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14161-46-7

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14161-46-7 Usage

Type of compound

Bicyclic organic compound

Structural features

Contains a cyclopropane ring
Contains an acetate group

Applications

Organic synthesis as a reagent
Formation of epoxides
Generation of carbenes

Industrial uses

Production of fragrances and flavorings
Pharmaceutical applications

Importance in organic chemistry

Potential as a chiral building block
Synthesis of complex molecules

Check Digit Verification of cas no

The CAS Registry Mumber 14161-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,6 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14161-46:
(7*1)+(6*4)+(5*1)+(4*6)+(3*1)+(2*4)+(1*6)=77
77 % 10 = 7
So 14161-46-7 is a valid CAS Registry Number.

14161-46-7SDS

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 acetic acid,7-oxabicyclo[4.1.0]heptan-6-ol

1.2 Other means of identification

Product number -
Other names 1-Acetoxycyclohexan-1,2-oxid

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:14161-46-7 SDS

14161-46-7Relevant articles and documents

-

Shine,Hunt

, p. 2434 (1958)

-

First lipase catalysed resolution of epoxy enol esters

Gravil, Sébastien,Veschambre, Henri,Chênevert, Robert,Bolte, Jean

, p. 6153 - 6157 (2007/10/03)

We report the first enzyme-catalysed kinetic resolution of epoxy enol esters. The lipase-promoted hydrolysis of these compounds provided α-hydroxyketones or α-hydroxyaldehydes (arising from the spontaneous rearrangement of the epoxy enols) and the residual esters with moderate to good enantioselectivity (E up to 100).

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