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
Appearance
Not specified in the material provided
Solubility
Not specified in the material provided
Boiling point
Not specified in the material provided
Melting point
Not specified in the material provided
Density
Not specified in the material provided
Stability
Not specified in the material provided
Toxicity
Not specified in the material provided
Environmental impact
Not specified in the material provided
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.
439667-21-7Relevant articles and documents
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.