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2-Cyclohexen-1-one, 3-methyl-2-(1-methylethyl)-, also known as 3-methyl-2-isopropylidene-cyclohexanone, is an organic compound with the molecular formula C10H16O. It is a colorless to pale yellow liquid with a strong, pungent odor. This chemical is a cyclic ketone derivative, featuring a cyclohexenone ring with a methyl group at the 3-position and an isopropylidene group at the 2-position. It is used as a fragrance ingredient and a synthetic intermediate in the production of various chemicals, particularly in the synthesis of musk compounds. Due to its potential to cause skin irritation and its classification as a sensitizer, it is important to handle this chemical with care, following proper safety procedures.

7291-87-4

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7291-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7291-87-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7291-87:
(6*7)+(5*2)+(4*9)+(3*1)+(2*8)+(1*7)=114
114 % 10 = 4
So 7291-87-4 is a valid CAS Registry Number.

7291-87-4SDS

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 3-methyl-2-propan-2-ylcyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 1-Methyl-2-methoaethyl-cyclohexen-(1)-on-(3)

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:7291-87-4 SDS

7291-87-4Relevant academic research and scientific papers

A Conformationally Defined 6-s-trans-Retinoic Acid Isomer: Synthesis, Chemopreventive Activity, and Toxicity

Vaezi, Michael F.,Alam, Muzaffar,Sani, Brahma P.,Rogers, Tina S.,Simpson-Herren, Linda,et al.

, p. 4499 - 4507 (2007/10/02)

A conformationally defined retinoic acid analog (1) which contains a dimethylene bridge to maintain the 6-s-trans orientation for two terminal double bonds in the polyene chain was synthesized.A Reformatsky reaction was utilized to extend the polyene chai

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