Lu, Ru-mei et al. published their research in Zhongcaoyao in 2014 | CAS: 10030-85-0

(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal hydrate (cas: 10030-85-0) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Computed Properties of C6H14O6

Chemical constituents of Gynostemma pentaphyllum was written by Lu, Ru-mei;Pan, Li-wei;Wei, Jian-hua;Zhong, Zhen-guo. And the article was included in Zhongcaoyao in 2014.Computed Properties of C6H14O6 This article mentions the following:

The chem. constituents of Gynostema pentaphyllum were studied. The chem. constituents were isolated and purified by silica gel, polyamide, and Sephadex LH-20 chromatog. Their structures were elucidated by physicochem. properties and spectral anal. Seventeen compounds were isolated and identified as dodecanoic acid (1), β-sitosterol (2), 3,3′,5-trihydroxy-4′,7-dimethoxyflavone (3), 1-2-benzenediol (4), 3′-O-methyltaxifolin (5), quercetin (6), rhamnetin (7), α-spinasterol-3-O-β-D-glucopyranoside (8), 3,4-dihydroxy benzoic acid (9), narcissoside (10), L-rhamnosemonohydrate (11), malonic acid (12), β-ethoxy-rutinoside (13), rutin (14), ombuoside (15), ginsenoside Rb1 (16), and β-daucosterol (17). Compound 1,3-5,7,9,10, and 12 are obtained from G. pentaphyllum for the first time. In the experiment, the researchers used many compounds, for example, (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal hydrate (cas: 10030-85-0Computed Properties of C6H14O6).

(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal hydrate (cas: 10030-85-0) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Computed Properties of C6H14O6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts