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396102-32-2

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396102-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 396102-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,6,1,0 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 396102-32:
(8*3)+(7*9)+(6*6)+(5*1)+(4*0)+(3*2)+(2*3)+(1*2)=142
142 % 10 = 2
So 396102-32-2 is a valid CAS Registry Number.

396102-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dimethoxy-5-methyl-3-(1,2,2-trimethylcyclopentyl)benzene

1.2 Other means of identification

Product number -
Other names Benzene,1,2-dimethoxy-5-methyl-3-(1,2,2-trimethylcyclopentyl)

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:396102-32-2 SDS

396102-32-2Relevant articles and documents

Total synthesis of (±)-herbertenediol

Srikrishna,Satyanarayana

, p. 2892 - 2900 (2007/10/03)

A formal total synthesis of the sesquiterpene (±)-herbertenediol and its dimers mastigophorenes A-D has been accomplished, starting from vanillin via 2,3-dimethoxy-5-methylbenzaldehyde. A combination of Claisen rearrangement and ring-closing metathesis reactions were employed for the generation of the two vicinal quaternary carbons on a cyclopentane ring.

New total synthesis of (±)-herbertene, (±)-β-herbertenol and (±)-herbertenediol

Gupta,Pal,Roy,Mukherjee

, p. 7563 - 7566 (2007/10/03)

The total syntheses of the herbertane sesquiterpenes (±)-herbertene (1), (±)-β-herbertenol (2) and (±)-herbertenediol (5) have been successfully accomplished involving copper-catalysed conjugate addition of Grignard reagents to unsaturated compounds and α

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