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CAS

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832-09-7

CIS-1,3-DIACETOXYCYCLOHEXANE is a cyclic organic compound with the molecular formula C10H16O4. It features a cyclohexane ring with two acetoxy groups attached in the cis configuration, making it a versatile reagent in organic synthesis.

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  • 832-09-7 Structure

  • Basic information

    1. Product Name: CIS-1,3-DIACETOXYCYCLOHEXANE
    2. Synonyms: CIS-1,3-DIACETOXYCYCLOHEXANE
    3. CAS NO:832-09-7
    4. Molecular Formula: C10H16O4
    5. Molecular Weight: 200.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 832-09-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: CIS-1,3-DIACETOXYCYCLOHEXANE(CAS DataBase Reference)
    10. NIST Chemistry Reference: CIS-1,3-DIACETOXYCYCLOHEXANE(832-09-7)
    11. EPA Substance Registry System: CIS-1,3-DIACETOXYCYCLOHEXANE(832-09-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 832-09-7(Hazardous Substances Data)

832-09-7 Usage

Uses

Used in Pharmaceutical and Biotechnology Industries:
CIS-1,3-DIACETOXYCYCLOHEXANE is used as a reagent in organic synthesis for the development of new drugs and biologically active compounds. Its unique structure allows for the formation of complex organic molecules, contributing to the advancement of pharmaceutical and biotechnological research.
Used in Perfume and Fragrance Production:
CIS-1,3-DIACETOXYCYCLOHEXANE is used as a component in the production of perfumes and fragrances. Its chemical properties enable the creation of various scent profiles, enhancing the variety and complexity of fragrances available in the market.
Used in Coatings and Adhesives Formulation:
CIS-1,3-DIACETOXYCYCLOHEXANE is also utilized in the formulation of certain types of coatings and adhesives. Its presence in these products contributes to their performance characteristics, such as adhesion strength and durability.

Check Digit Verification of cas no

The CAS Registry Mumber 832-09-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 832-09:
(5*8)+(4*3)+(3*2)+(2*0)+(1*9)=67
67 % 10 = 7
So 832-09-7 is a valid CAS Registry Number.

832-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1S,3R)-3-acetyloxycyclohexyl] acetate

1.2 Other means of identification

Product number -
Other names cis-Cyclohexan-1,3-dioldiacetat

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:832-09-7 SDS

832-09-7Downstream Products

832-09-7Relevant articles and documents

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

Rhodium(I)- and iridium(I)-catalyzed hydroboration reactions: Scope and synthetic applications

Evans, David A.,Fu, Gregory C.,Hoveyda, Amir H.

, p. 6671 - 6679 (2007/10/02)

A study of the rhodium(I)- and iridium(I)-catalyzed hydroboration of olefins with catecholborane is described. Applications to organic synthesis were one focus of this investigation. The scope of the reaction was defined, and issues of stereoselection were addressed. The rhodium-catalyzed hydroboration of several classes of allylic alcohols was found to be highly diastereoselective, preferentially affording the isomer complementary to that furnished by the uncatalyzed variant of the reaction (9-BBN). The first two general approaches to effecting a directed olefin hydroboration were developed. Both phosphinites and amides proved capable of delivering the transition metal reagent.

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