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6-METHYLCYCLOHEX-3-ENECARBOXYLIC ACID is a cyclic organic compound characterized by a 6-carbon ring with a methyl group and a double bond, featuring a carboxylic acid functional group. It is classified as a cycloalkene carboxylic acid and is known for its structural and reactive properties, making it a valuable intermediate in the synthesis of various organic compounds.

92284-35-0

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92284-35-0 Usage

Uses

Used in Pharmaceutical Industry:
6-METHYLCYCLOHEX-3-ENECARBOXYLIC ACID is used as an intermediate in the synthesis of drugs, leveraging its reactivity and structural properties to contribute to the development of pharmaceutical compounds.
Used in Chemical Industry:
In the chemical industry, 6-METHYLCYCLOHEX-3-ENECARBOXYLIC ACID serves as a building block in organic synthesis, enabling the creation of more complex structures and contributing to the production of fragrances and other fine chemicals.
Used in Organic Synthesis:
6-METHYLCYCLOHEX-3-ENECARBOXYLIC ACID is utilized as a versatile chemical compound in organic synthesis, where it aids in constructing intricate molecular structures that are essential in various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 92284-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,8 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92284-35:
(7*9)+(6*2)+(5*2)+(4*8)+(3*4)+(2*3)+(1*5)=140
140 % 10 = 0
So 92284-35-0 is a valid CAS Registry Number.

92284-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-METHYLCYCLOHEX-3-ENECARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names trans-2-methylcyclohex-2-ene 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:92284-35-0 SDS

92284-35-0Relevant academic research and scientific papers

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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