Category: 2160-93-2

Purt, G. published an article in 1962, the title of the article was The binary system BaO-WO3.Formula: C8H19NO2 And the article contains the following content:

With more than 40 samples of different compositions, the equilibrium diagram BaO-WO3 could be established, m.p. determinations and Debye-Scherrer pictures being used. Two congruently melting compounds appear, leading to 3 eutectics in the system. The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).Formula: C8H19NO2

2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Formula: C8H19NO2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Fishbein, Lawrence; Cavanaugh, M. A. published an article in 1965, the title of the article was Detection and paper chromatography of N-substituted hydroxy, 2-hydroxyethyl, 2-chloroethyl, and N,N-bis(2-hydroxyethyl) derivatives.Product Details of 2160-93-2 And the article contains the following content:

Studies of the metabolism, degradation, and mutagenicity of N-substituted 2-hydroxyethyl, and 2-chloroethyl pesticides, N-hydroxy carbamates and related N and C substituted OH derivatives prompted the need to evaluate various categories of detecting reagents as to their possible utility for subsequent differentiation, and identification of the above moieties in a variety of aliphatic, aromatic, and cyclic compounds One-dimensional descending chromatography was carried out on Whatman Number 1 filter paper by using the following solvent systems: BuOH-HOAc-H2O (5:1:4); BuOH-EtOH-H2O (7:1:2); and iso-PrOH-NH4OH-H2O (80:5:15). Detecting reagents were: (1) 5% Na nitroprusside-10% MeCHO mixed with an equal volume of 2% aqueous Na2CO3; (2) FCNP reagent (mixture of equal volumes of 10% NaOH, 10% Na nitroprusside, and 10% K ferricyanide diluted with 3 volumes of H2O, and mixed with an equal volume of Me2CO); (3) 0.2% ninhydrin in Me2CO; (4) 0.2% ninhydrin in Me2CO with 5% C5H5N; (5) 1% FeCl3 in MeOH; (6) 10% p-dimethylaminobenzaldehyde in 1:4 Me2CO-concentrated HCl; (7) 2 ml. trans-cinnamaldehyde in 95 ml. EtOH, 18.5 ml. H2O, and 6 ml. concentrated HCl; (8) 5% 4-(p-nitrobenzyl)pyridine in Me2CO; (9) 0.5% barbituric acid in EtOH containing 2 ml. 85% H3P4O (10) equal volumes of C5H5N and MeCHO; (11) 1% isatin in iso-PrOH containing 1% C5H5N and 1.5% Zn(OAc)2; (12) 0.5% Cu(OAc)2 in EtOH containing 0.1% Me2NH and 2% (HOC2H4)3N; (13) 0.5 % 2,6-dibromo-N-chloro-p-quinone imine in 4:1 dioxane-Me2CO; (14) 5% N,2,6-trichlorobenzoquinone imine in 4:1 dioxane-Me2CO; (15) 3% K nitrosodisulfonate in N NaOH; (16) 1% KMnO4. The Rf values and color of spots with the reagents are given for 76 N and C substituted N-hydroxy, 2-hydroxyethyl, 2-chloroethyl, and N,N-bis(2-hydroxyethyl) derivatives and related compounds The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).Product Details of 2160-93-2

2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Product Details of 2160-93-2

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Alcohol – Wikipedia,
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Liteanu, C.; Gocan, S. published an article in 1961, the title of the article was Paper thermochromatography. I. Separation of the mixture Cu++ and Cd++ with butanol + HCl.Category: alcohols-buliding-blocks And the article contains the following content:

Rf values change as the temperature gradient increases. Changes in Rf values for Cd++ and Cu++ are different in 80% butanol + 3N 20% HCl, so that better separation is obtained. The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).Category: alcohols-buliding-blocks

2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
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Chremos, George N.; Zimmerman, Howard K. published an article in 1962, the title of the article was Protolysis equilibrium of N-substituted diethanolamines.Formula: C8H19NO2 And the article contains the following content:

Limiting pK values for the acidic dissociation of 6 N-substituted diethanolammonium ions in sq. solution are given, each at a series of temperatures in the range 15-55掳. The effect of the 3rd substituent on the N atom on the equilibrium appears to be chiefly an influence on the mutual interaction between the 2 hydroxyethyl groups present in each mol., although the ex- pected basicity-depressing effects are also found for the N-phenyl and N-benzyl compounds The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).Formula: C8H19NO2

2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Formula: C8H19NO2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Mazitova, F. N.; Ermakova, S. K.; Virobyants, R. A. published an article in 1962, the title of the article was The analysis of gaseous hydrocarbons by chromatographic adsorption on alumina.HPLC of Formula: 2160-93-2 And the article contains the following content:

cf. Korol, CA 54, 18176f; Kondrat’ev, et al., CA 54, 8468a. By use of 20-50 mesh Al2O3, to which 2% silicone oil (MS-2) has been added in a 6 mm. 脳 2 m. column at 30掳, the separation at a gas-carrier velocity of 50 cc./mm. of a mixture of 11 C1-4 gases is accomplished in 1 hr. A microflame detector with a registering instrument is illustrated. The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).HPLC of Formula: 2160-93-2

2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. HPLC of Formula: 2160-93-2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Valkenburg, Alvin Van Jr. published an article in 1962, the title of the article was Visual observations of high-pressure transitions.Synthetic Route of 2160-93-2 And the article contains the following content:

Phase changes in transparent solids and liquids were visually observed with microscopic techniques by means of a diamond “squeezer” high-pressure cell (Lippincott, et al., CA 55, 17211b). Pressures up to 115 kilobars were obtained and observations were made with a polarizing microscope focused through I diamond onto the surface of the specimen. Transitions in AgBr at 86 kilobars and room temperature and in KNO3 are illustrated. At least 2 crystalline ice phases were detected in H2O frozen at room temperature The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).Synthetic Route of 2160-93-2

2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Synthetic Route of 2160-93-2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Zimmerman, Howard K. Jr.; Cosmatos, Alexandros published an article in 1962, the title of the article was Migration of amino alcohols on paper.Name: 2,2′-(tert-Butylazanediyl)diethanol And the article contains the following content:

Rf values are tabulated for 69 amino alcs. on Whatman Number 1 paper with the following solvent systems: 77:6:17 BuOH:AcOH:H2O, BuOH saturated with 0.1% NH4OH, and 42:25:25:8 C5H5N:EtOAc:H2O:AcOH. Variations in migration rates with structural characteristics of the alcs. are briefly discussed. The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).Name: 2,2′-(tert-Butylazanediyl)diethanol

2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Name: 2,2′-(tert-Butylazanediyl)diethanol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Ishidate, Morizo; Sakurai, Yoshio; Aiko, Isao published an article in 1960, the title of the article was Cancerocidal substances. XXVI. Preparation of bis(2-chloroethyl)amine derivatives and related N-oxides.COA of Formula: C8H19NO2 And the article contains the following content:

Fourteen new RN(CH2CH2Cl)2 (I) and 6 of their N-oxides were prepared and tested for their in vivo and in vitro antitumor activity against the Yoshida sarcoma. The methods used were previously described (CA 49, 8304h). The intermediate RN(CH2CH2OH)2 (II) were prepared by either method A, [RX + HN(CH2CH2OH)2], or method B, (RNH2 + 2CH2.CH2O) (R, method used, phys. constants of II or its derivatives given): tert-Bu, B, b8 132-5掳; C12H25, A or B, b4 200-10掳; 2-(10-phenothiazinyl)ethyl (III), A, b0.02 250-60掳; 9-camphoryl (IV), B, HCl salt m. 218-20掳 (decomposition), picrate m. 116-19掳; MeOCH2CH2, A, b4 133-40掳; BuOCH2CH2, A, b7 154-60掳; PhOCH2CH2, A, b4 200-10掳; (MeO)2CHCH2, A, b4 127-33掳, b5 165-9掳; (EtO)2CHCH2, A, b4 138-42掳, b4 161-5掳; and (BuO)2CHCH2, A, b4 175-6掳. II were chlorinated without further purification to give I, which were oxidized to the corresponding N-oxides in 6 cases (R, phys. constants of I or its derivatives given): tert-Bu (30% yield), HCl salt m. 178-9掳, N-oxide (48%) picrate m. 95-6掳, and HCl salt m. 89掳; C6H13, b7.5 125-9掳, HCl salt m. 78-82掳; C12H25, picrylsulfonate m. 92-3掳; III, HCl salt m. 96-8掳; IV, HCl salt m. 218-20掳 (decomposition), [伪]23D -60.6掳 (c 1.58, H2O), N-oxide HCl salt m. 178-80掳 (decomposition); MeOCH2CH2, HCl salt m. 130掳, N-oxide HCl salt m. 109-11掳 and picrate m. 89-90掳; BuOCH2CH2, HCl salt m. 126-7掳, N-oxide HCl salt m. 75-6掳, and picrate m. 81-2掳; PhOCH2CH2, HCl salt m. 150-1掳, picrate m. 117-18掳, N-oxide HCl salt m. 173-4掳 (decomposition) and picrate m. 126-7掳; (MeO)2CHCH2, HCl salt m. 129-30掳, N-oxide HCl salt m. 110掳 and picrate m. 89-90掳; (EtO)2CHCH2, HCl salt m. 132-3掳; and (BuO)2CHCH2, b3 111-13掳, HCl salt m. 121-2掳. The 3 remaining compounds of this series were: the N-oxide of I (R = EtOCH2CH2), which had been previously prepared (loc. cit.); I (R = OHCCH2) (picrate m. 131掳), prepared by hydrolysis of I [R = (MeO)2CHCH2] by heating it 5 hrs. at 80掳 with 20% HCl; and I (R = AcCH2CH2) (picrate m. 113-15掳), prepared by warming 1.5 hrs. at 40-5掳 41 g. HCl salt of I (R = H) with 23 cc. 30% HCHO, and 95 cc. Me2CO. The 9-aminocamphor (m. 172掳; HCl salt m. 334掳 (decomposition); toluenesulfonamide m. 182掳) for the preparation of II (R = IV) was prepared in 70 g. yield by the catalytic hydrogenation (Raney Ni) of a mixture of 71 g. 9-oxocamphor oxime and 100 g. liquid NH3 in 300 cc. EtOH. The results of tests of these 20 compounds for biol. activity and toxicity were reported and discussed. A few were very effective against Yoshida sarcoma. The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).COA of Formula: C8H19NO2

2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. COA of Formula: C8H19NO2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Psarras, Theodore G.; Zimmerman, Howard K. Jr.; Rasiel, Yecheskel; Weidmann, Hans published an article in 1962, the title of the article was Amino alcohol esters of hydroxy boranes. VI. diptych-Boroxazolidines.Related Products of 2160-93-2 And the article contains the following content:

cf. CA 56, 12915d. The rates of hydrolysis (results tabulated) of the N 鈫?B bonds of 12 diptyvh-boroxazolidines (I) in 90% Me2CO were determined The results indicated that the rates of hydrolysis were chiefly a function of the size of the substituents on the N atom and that the substituents on the ester C atom exerted only a secondary effect. The new I were prepared by azeotropic estcrification of the appropriate amino alc. with phenyldihydroxyborane anhydride. The mol. weights (determined by the Rast method) confirmed the monomeric character of the I with exception of the diptych-boroxazolidine of RN(CH2CH2OH)2 (II) (R = H), which was dimeric (mol. weight 379). The following newly prepared I were reported (amino alc. used, % yield, and m.p. given): PhCH2N(CH2CH2OH)2, 91, 196.5掳 (C6H6); tert-BuN(CH2CH2OH)2, 81, 189掳 (MeCN); HN(CH2CHMeOH)2, 100, 251-2掳 (C6H6); [(HOCH2CH2)2NCH2]2, 86, 204掳 (MeCN); (HOCHMeCH2)2NCH2CH2N(CH2CHMeOH)CH2CH2OH, 100, 280掳 (decomposition) (MeCN); [(HOCH-MeCH2)2NCH2]2, 94, 302掳 (decomposition) (MeCN); [(HOCHEtCH2)2NCH2]2, 66, 277掳 (EtOAc). The following I were also investigated (amino alc. given): II (R = H); II [R = Me); II (R = Et); II (R = Bu); II (.R = iso-Pr). The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).Related Products of 2160-93-2

2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Related Products of 2160-93-2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Gelbard, Georges; Rumpf, Paul published an article in 1969, the title of the article was N-Alkylated diethylenetriamines and triethylenetetramines.Electric Literature of 2160-93-2 And the article contains the following content:

The synthesis of polyamines H2N(CH2)2(NHCH2CH2)nNH2 selectively alkylated on the terminal NH2 group by reductive alkylation with ketones. With diethylenetriamine good yields of 1,7-dialkylated polyamines were obtained. Also, 1,10-dialkylated polyamines were obtained with triethylenetetramine. With excess NH3, the yield of dialkylated product decreased in favor of monoalkylated polyamines. The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).Electric Literature of 2160-93-2

2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Electric Literature of 2160-93-2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts