Category: 100-55-0

Recommanded Product: 3-PyridinemethanolIn 2021 ,《Synthesis of TEMPO radical decorated hollow porous aromatic frameworks for selective oxidation of alcohols》 was published in Chemical Communications (Cambridge, United Kingdom). The article was written by Shen, Yan-Ming; Xue, Yun; Yan, Mi; Mao, Hui-Ling; Cheng, Hu; Chen, Zhuo; Sui, Zhi-Wei; Zhu, Shao-Bin; Yu, Xiu-Jun; Zhuang, Jin-Liang. The article contains the following contents:

A bottom-up approach was developed to prepare TEMPO radical decorated hollow aromatic frameworks (HPAF-TEMPO) by using TEMPO radical functionalized monomers and SiO2 nanospheres as templates. The accessible inner layer, high d. of TEMPO sites, and hybrid micro-/mesopores of the HPAF-TEMPO enable the aerobic oxidation of a broad range of alcs. with high efficiency and excellent selectivity. The experimental process involved the reaction of 3-Pyridinemethanol(cas: 100-55-0Recommanded Product: 3-Pyridinemethanol)

3-Pyridinemethanol(cas: 100-55-0) belongs to pyridine. Pyridines, quinolines, and isoquinolines have found a function in almost all aspects of organic chemistry. Pyridine has found use as a solvent, base, ligand, functional group, and molecular scaffold. As structural elements, these moieties are potent electron-deficient groups, metal-directing functionalities, fluorophores, and medicinally important pharmacophores. Recommanded Product: 3-Pyridinemethanol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Related Products of 100-55-0In 2021 ,《A predictive model for additions to N-alkyl pyridiniums》 appeared in Chemical Communications (Cambridge, United Kingdom). The author of the article were Knight, Brian J.; Tolchin, Zachary A.; Smith, Joel M.. The article conveys some information:

Disclosed in this communication is a thorough study on the dearomative addition of organomagnesium nucleophiles to N-alkyl pyridinium electrophiles. The regiochem. outcomes have observable and predictable trends associated with the substituent patterns on the pyridinium electrophile. Often, the substituent effects can be either additive, giving high selectivities, or ablative, giving competing outcomes. Addnl., the nature of the organometallic nucleophilic component was also investigated for its role in the regioselective outcome. The effects of either reactive component are important to both the overall reactivity and site of nucleophilic addition The utility of these observed trends is demonstrated in a concise, dearomative synthesis of a tricyclic compound shown to have insecticidal activity. In the experiment, the researchers used many compounds, for example, 3-Pyridinemethanol(cas: 100-55-0Related Products of 100-55-0)

3-Pyridinemethanol(cas: 100-55-0) belongs to pyridine. The basicity and metallophilic high donor number of these π-deficient systems has long favored them as ligands in metal catalysis. The last decade saw pyridine assume a stronger role as functional group for directed C–H oxidation/activation.Related Products of 100-55-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

HPLC of Formula: 100-55-0In 2021 ,《KF/clinoptilolite NPs: An efficient and heterogeneous catalyst for chemoselective silylation of alcohols and phenols》 appeared in Phosphorus, Sulfur and Silicon and the Related Elements. The author of the article were Oladee, Razieh; Zareyee, Daryoush; Khalilzadeh, Mohammad A.. The article conveys some information:

Potassium fluoride incorporated on clinoptilolite nanoparticles (KF/CP NPs) by ion exchanging is found to be an effective and inexpensive heterogeneous nanocatalyst for chemoselective silylation of alcs. and phenols with 1,1,1,3,3,3-hexamethyldisilazane (HMDS) at room temperature Nano-powder of clinoptilolite (CP) was prepared using a planetary ball mill mech. method and characterized by dynamic light scattering (DLS), X-ray powder diffraction (XRD) and scanning electron microscope (SEM) analyses. Almost all of products were obtained in high yields as well as short reaction times and the catalyst was also reused eight times without loss of its catalytic activity. In the experiment, the researchers used many compounds, for example, 3-Pyridinemethanol(cas: 100-55-0HPLC of Formula: 100-55-0)

3-Pyridinemethanol(cas: 100-55-0) belongs to pyridine. Pyridine derivatives lend themselves to many roles in the spirited field of supramolecular chemistry – whether as the ligand backbone of metal-organic polymers or presiding over the key electronic stations of nanodevices. In biochemistry, pyridine-containing cofactors are necessary nutrients on which our lives depend. HPLC of Formula: 100-55-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

《Pyridinium salts of dithiophosphoric acids on the basis of nicotinic acids and their isomers, 3-hydroxypyridine, and 3-pyridinemethanol》 was published in Phosphorus, Sulfur and Silicon and the Related Elements in 2020. These research results belong to Nizamov, Ilyas S.; Salikhov, Ramazan Z.; Timushev, Ildus D.; Nikitin, Yevgeniy N.; Nizamov, Ilnar D.; Yakimov, Vladimir Yu.; Shulaeva, Marina P.; Pozdeev, Oscar K.; Batyeva, Elvira S.; Cherkasov, Rafael A.; Ponomareva, Anna S.. Quality Control of 3-Pyridinemethanol The article mentions the following:

A new series of chiral carboxypyridinium dithiophosphates I (R = pyridin-2-yl, pyridin-3-yl, pyridin-4-yl) was synthesized by the reactions of acids RC(O)OH with dithiophosphoric acid on the basis (1S)-endo-(-)-borneol in benzene or ethanol. The compound 5,5-dimethyl-2-mercapto-2-thiono-1,3,2-dioxaphosphorinane reacted with 3-hydroxypyridine or 3-pyridinemethanol in EtOH to afford the 3-hydroxypyridinium/3-hydroxymethylpyridinium 5,5-dimethyl-2-mercapto-2-thiono-1,3,2-dioxaphosphorinane which possessed antifungal activity against Candida albicans. The results came from multiple reactions, including the reaction of 3-Pyridinemethanol(cas: 100-55-0Quality Control of 3-Pyridinemethanol)

3-Pyridinemethanol(cas: 100-55-0) belongs to pyridine. Pyridines are often used as catalysts or reagents; particular notice has been paid recently to how pyridine coordinates to metal centers enabling a wide range of valuable reactions. Quality Control of 3-Pyridinemethanol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts