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Cyclohexane-1,3-diyl diacetate, also known as 1,3-diacetoxycyclohexane, is an organic compound with the chemical formula C10H16O4. It is a colorless liquid that is derived from cyclohexane, a cyclic hydrocarbon, by the substitution of two hydrogen atoms at positions 1 and 3 with acetate groups. cyclohexane-1,3-diyl diacetate is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Cyclohexane-1,3-diyl diacetate is known for its reactivity and can undergo various chemical transformations, making it a valuable building block in organic chemistry.

6939-74-8

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6939-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6939-74-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6939-74:
(6*6)+(5*9)+(4*3)+(3*9)+(2*7)+(1*4)=138
138 % 10 = 8
So 6939-74-8 is a valid CAS Registry Number.

6939-74-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-acetyloxycyclohexyl) acetate

1.2 Other means of identification

Product number -
Other names optically inactive 1.3-diacetoxy-cyclohexane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6939-74-8 SDS

6939-74-8Relevant academic research and scientific papers

METHOD FOR THE PRODUCTION OF DIARYLCYCLOALKYL DERIVATIVES

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Page/Page column 14, (2010/11/28)

The invention relates generally to a process for preparing diarylcycloalkyl derivatives of the formula (I). wherein the respective R-group substituents are defined herein. These compounds of formula (I) are activators for peroxisome proliferator-activated

Enzymatic resolution, desymmetrization, and dynamic kinetic asymmetric transformation of 1,3-cycloalkanediols

Fransson, Ann-Britt L.,Xu, Yongmei,Leijondahl, Karin,Baeckvall, Jan-E.

, p. 6309 - 6316 (2007/10/03)

An efficient desymmetrization of cis-1,3-cyclohexanediol to (1S,3R)-3-(acetoxy)-1-cyclohexanol ((R,S)-2a) was performed via Candida antarctica lipase B (CALB)-catalyzed transesterification, in high yield (up to 93%) and excellent enantioselectivity (ee's

OXYGENATION OF AROMATIC AND ALIPHATIC HYDROCARBONS BY A NEW REAGENT SYSTEM, Fe(CH3CN)6(2+)-H2O2-Ac2O: AN EFFECTIVE MODEL REAGENT FOR MONO-OXYGENASE

Kotani, Eiichi,Kobayashi. Shigeki,Ishii, Yoko,Tobinaga, Seisho

, p. 4671 - 4679 (2007/10/02)

Reactions of aromatic and aliphatic hydrocarbons with a new system, Fe(CH3CN)6(2+) - H2O2 - Ac2O in CH3CN, gave oxygenation products with fairly high reaction efficiency ( Tables I and II )compared to known to reagent systems used as enzyme models for mono-oxygenases.Investigations of the mechanism of these reactions indicated the involvement of either complex C.FeIV(OH)(OAc)(2+), or complex D, FeIV(OAc)(2+), dependig on the organic substrate.Keywords-oxygenation; aromatic hydrocarbon; aliphatic hydrocarbon; hexakisacetonitrile iron(II) perchlorate; hydrogen peroxide; enzyme model; mono-oxygenase

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