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2-Cyclohepten-1-one, 2-bromo-3-methyl-6-(1-methylethenyl)-, (6R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

322000-37-3

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322000-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 322000-37-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,2,0,0 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 322000-37:
(8*3)+(7*2)+(6*2)+(5*0)+(4*0)+(3*0)+(2*3)+(1*7)=63
63 % 10 = 3
So 322000-37-3 is a valid CAS Registry Number.

322000-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (6R)-2-bromo-3-methyl-6-prop-1-en-2-ylcyclohept-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Cyclohepten-1-one,2-bromo-3-methyl-6-(1-methylethenyl)-,(6R)

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:322000-37-3 SDS

322000-37-3Downstream Products

322000-37-3Relevant academic research and scientific papers

Enantiodivergent syntheses of cycloheptenone intermediates for guaiane sesquiterpenes

Leiva de Faria, Mary,De A. Magalhaes, Ruy,Silva, Fernando C,De O. Matias, Luiz G,Ceschi, Marco A,Brocksom, Ursula,John Brocksom, Timothy

, p. 4093 - 4103 (2007/10/03)

The syntheses of enantiomeric 6-isopropenyl-3-methyl-2-cycloheptenones 16 and 22 have been effected starting from (R)-(-)-carvone. In the synthesis of 16, (R)-(-)-carvone was reduced and the resulting dihydrocarvone transformed regioselectively into silyl

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