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10479-42-2

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10479-42-2 Usage

General Description

Trans-6-methylcyclohex-3-ene-1-carboxylic acid is a chemical compound with a molecular formula C8H12O2. It is a carboxylic acid derivative and belongs to the cyclohexene family. trans-6-methylcyclohex-3-ene-1-carboxylic acid has a trans configuration, indicating that the methyl group and the carboxylic acid group are on opposite sides of the double bond in the cyclohexene ring. It is commonly used in organic synthesis and can be involved in various chemical reactions to produce other compounds. Its specific properties and potential uses depend on the context and application within the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 10479-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,7 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10479-42:
(7*1)+(6*0)+(5*4)+(4*7)+(3*9)+(2*4)+(1*2)=92
92 % 10 = 2
So 10479-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O2/c1-6-4-2-3-5-7(6)8(9)10/h2-3,6-7H,4-5H2,1H3,(H,9,10)/t6-,7-/m1/s1

10479-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name siglure acid

1.2 Other means of identification

Product number -
Other names (1R,6R)-6-METHYLCYCLOHEX-3-ENE-1-CARBOXYLIC ACID

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:10479-42-2 SDS

10479-42-2Relevant articles and documents

STUDIES OF COMPOUNDS IN THE MENTHANE SERIES. XIX. SYNTHESIS AND PROPERTIES OF TRANS-o-4-MENTHEN-8-OL AND STEREOISOMERIC o-5-METHEN-8-OLS

Bazyl'chik, V. V.,Fedorov, P. I.,Klyuev, N. A.,Dank, E. Kh.

, p. 1320 - 1327 (2007/10/02)

Trans-o-4-Menthen-8-ol and cis- and trans-o-5-menthen-8-ols have been prepared via the Diels-Alder reactions of 1,3-butadiene with crotonaldehyde in the presence of boron trifluoride etherate, and piperylene with methyl acrylate, respectively.The dehydration reactions of these alcohols have been studied in the presence of acetic anhydride and potassium bisulfate; the latter reagent demonstrates a high reaction selectivity.

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