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3492-41-9

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3492-41-9 Usage

Uses

Solvent in industrial applications; production of perfumes, flavors, and in the pharmaceutical and cosmetic industries

Physical Properties

Colorless liquid; fruity odor

Flammability

Flammable

Health Hazards

Potential health hazards; precautions should be taken when handling

Reaction

Derived from the esterification of 3-bromo-2,2-dimethyl-1-propanol with acetic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 3492-41-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,9 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3492-41:
(6*3)+(5*4)+(4*9)+(3*2)+(2*4)+(1*1)=89
89 % 10 = 9
So 3492-41-9 is a valid CAS Registry Number.

3492-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid (3-bromo-2,2-dimethyl-1-propyl)ester

1.2 Other means of identification

Product number -
Other names 3-Brom-2,2-dimethyl-propylacetat

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:3492-41-9 SDS

3492-41-9Relevant articles and documents

Asymmetric Synthesis of (+)-Hirsutene

Hua, Duy H.,Venkataraman, S.,Ostrander, Robert A.,Sinai, Gurudas-Z.,McCann, Peggy J.,et al.

, p. 507 - 515 (2007/10/02)

The asymmetric total synthesis of (+)-hirsutene from the regio- and enantioselective 1,4-γ-addition reaction of (-)-(S)-allyl p-tolyl sulfoxide and 2-methyl-2-cyclopentenone is presented.In this total synthesis, a facile ring closure reaction involving enol thioether and enol acetate moieties and the deoxygenation reaction of a highly hindered secondary alcohol via its 2-propanesulfonate were found.An unexpected displacement reaction at the sulfur atom of alkenyl sulfoxides and the addition reactions of the cis sulfinylallyl anions with cyclic enones were also observed during the studies.

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