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Silane, trimethyl[(3-pentyl-1-cyclohexen-1-yl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92210-69-0

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92210-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92210-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,1 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92210-69:
(7*9)+(6*2)+(5*2)+(4*1)+(3*0)+(2*6)+(1*9)=110
110 % 10 = 0
So 92210-69-0 is a valid CAS Registry Number.

92210-69-0SDS

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 trimethyl-(3-pentylcyclohexen-1-yl)oxysilane

1.2 Other means of identification

Product number -
Other names -

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:92210-69-0 SDS

92210-69-0Relevant articles and documents

CYCLOHEXANE ANALOGS OF POISON IVY AND POISON OAK DERIVATIVES. A TOTALLY STEREOSELECTIVE SYNTHESIS OF TRANS,TRANS-3-ALKYL-1,2-CYCLOHEXANEDIOLS.

Lepoittevin, Jean-Pierre,Benezra, Claude

, p. 2505 - 2506 (1984)

Pure trans,trans-3-methyl-, 3-n-pentyl-, 3-n-decyl- and 3-n-pentadecyl-1,2-cyclohexanediols have been prepared in two steps, in 55-70percent overall yields from 2-cyclohexenone.

Saturated analogues of poison ivy allergens. Synthesis of trans,trans- and cis,trans-3-alkyl-1,2-cyclohexanediols and sensitizing properties in allergic contact dermatitis

Lepoittevin,Benezra

, p. 287 - 291 (2007/10/02)

Saturated analogues of poison ivy and oak allergens (3-alkylcatechols), i.e. trans,trans-3-alkyl-1,2-cyclohexanediols (alkyl = CH3, n-C5H11, n-C10H21, n-C15H31), have been prepared and used to sensitize guinea pigs. Only long-chain derivatives (carbon chain length > C10) are contact sensitizers. The sensitized animals cross-react to PDC (i.e. pentadecylcatechol, one of the allergens of poison ivy), but the converse is not true (PDC-sensitized animals do not react to cyclohexanediols). cis,trans-3-n-Pentadecyl-1,2-cyclohexanediol has also been synthesized and shown to be a sensitizer. There is not cross-reaction between trans,trans- and cis,trans-3-n-pentadecylcyclohexanediols, excluding a common skin metabolite.

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