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1,2,3-Cyclohexanetriol, 1-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

439667-21-7

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439667-21-7 Usage

Structure

Cyclohexane ring with three hydroxyl groups and one methyl group attached

Type

Cyclic polyol derivative

Functional groups

Three hydroxyl (-OH) groups and one methyl (-CH3) group

Applications

a. Production of pharmaceuticals
b. Fragrances
c. Chemical intermediate in organic synthesis

Reactivity

Versatile compound due to the presence of three hydroxyl groups

Safety

Handle with care and follow safety guidelines in a laboratory setting

Check Digit Verification of cas no

The CAS Registry Mumber 439667-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,6,6 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 439667-21:
(8*4)+(7*3)+(6*9)+(5*6)+(4*6)+(3*7)+(2*2)+(1*1)=187
187 % 10 = 7
So 439667-21-7 is a valid CAS Registry Number.

439667-21-7Downstream Products

439667-21-7Relevant academic research and scientific papers

Regio- And Stereoselective Addition of HO/OOH to Allylic Alcohols

Wang, Xiao-Tao,Han, Wei-Bo,Chen, Hui-Jun,Zha, Qinghong,Wu, Yikang

, p. 10007 - 10021 (2020/08/28)

A range of allylic alcohols are shown to readily react with ethereal H2O2 in the presence of catalytic amounts of Na2MoO4-gly or MoO2(acac)2, affording the C═C trans hydroxylation-hydroperoxylation products in good yields with high regio- and stereoselect

THE SYNTHESIS OF CHIRAL ISOPROPYLIDENE DERIVATIVES OF 1,2,3-CYCLOHEXANETRIOLS BY ENZYMATIC DIFFERENTIATION

Dumortier, L.,Eycken, J. Van der,Vandewalle, M.

, p. 3201 - 3204 (2007/10/02)

2,3-O-Isopropylidene-1-cyclohexanol chiral building blocks have been prepared with high enantiomeric purities by enzymatic hydrolysis of their racemic acetates or n.butyrates.

ON STEREOCHEMISTRY OF OSMIUM TETRAOXIDE OXIDATION OF ALLYLIC ALCOHOL SYSTEMS. EMPIRICAL RULE

Cha, J. K.,Christ, W. J.,Kishi, Y.

, p. 2247 - 2256 (2007/10/02)

An empirical formulation is presented to predict the stereochemistry of major osmylation products of allylic alcohols and their derivatives.

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