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66049-63-6

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66049-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66049-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,4 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66049-63:
(7*6)+(6*6)+(5*0)+(4*4)+(3*9)+(2*6)+(1*3)=136
136 % 10 = 6
So 66049-63-6 is a valid CAS Registry Number.

66049-63-6SDS

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 cis-[(3,5-dimethyl-1-cyclohexen-1-yl)oxy]trimethylsilane

1.2 Other means of identification

Product number -
Other names cis-3,5-Dimethyl-1-((trimethylsilyl)oxy)-1-cyclohexene

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:66049-63-6 SDS

66049-63-6Relevant articles and documents

Synthesis of syn-4,6-dimethyldodecanal, the male sex pheromone and trail-following pheromone of two species of the termite Zootermopsis

Ghostin,Bordereau,Braekman

, p. 560 - 568 (2011/05/12)

Recently, we reported that syn-4,6-dimethyldodecanal is the male sex pheromone and the trail-following pheromone of the Termopsidae Zootermopsis nevadensis and Zootermopsis angusticollis. In this article, we describe the syntheses of the mixture of the fo

Enantioselective Formation of cis-3,5-Dimethylcyclohexanone Lithium Enolate and Stereoselective Aldol Reaction with Benzaldehyde

Majewski, Marek,Gleave, D. Mark

, p. 3599 - 3605 (2007/10/02)

Deprotonation of cis-3,5-dimethylcyclohexanone (6) with chiral lithium amide bases 10-12 has been investigated.The resulting lithium enolates 7a,b react with benzaldehyde, acetic anhydride, or trimethylsilyl chloride to yield, respectively, the aldols 8 a

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