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3-Hexanone, 6-bromo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20434-22-4

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20434-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20434-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,3 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20434-22:
(7*2)+(6*0)+(5*4)+(4*3)+(3*4)+(2*2)+(1*2)=64
64 % 10 = 4
So 20434-22-4 is a valid CAS Registry Number.

20434-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromohexan-3-one

1.2 Other means of identification

Product number -
Other names 3-Hexanone,6-bromo

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:20434-22-4 SDS

20434-22-4Relevant academic research and scientific papers

C3-homologation. Synthesis of C19-skipped polyenic pheromones

Viala,Munier,Santelli

, p. 3347 - 3352 (2007/10/02)

Total synthesis of three sex pheromone components including an all-cis diene or triene unit are described. Starting from decanal, cis-Wittig reactions, by using C3 homologating agent 4 and convenient phosphonium salts, allowed us to built up all-cis skipp

LES ORGANOCUPRATES DANS UNE NOUVELLE SYNTHESE D'AMINOACIDES ENANTIOMERIQUEMENT PURS

Bajgrowicz, J. A.,Hallaoui, A. El,Jacquier, R.,Pigiere, Ch.,Viallefont, Ph.

, p. 1833 - 1845 (2007/10/02)

A new general method of synthesis of optically pure α- amino esters was elaborated during studies on the reaction of organocuprates with tosyl and halogeno derivatives of L-serine and L-homoserine.

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