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2-Cyclohexen-1-one, 3-methyl-5-(1-methylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98909-91-2

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98909-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98909-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,9,0 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98909-91:
(7*9)+(6*8)+(5*9)+(4*0)+(3*9)+(2*9)+(1*1)=202
202 % 10 = 2
So 98909-91-2 is a valid CAS Registry Number.

98909-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-Methyl-5-isopropenyl-2-cyclohexen-1-on

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:98909-91-2 SDS

98909-91-2Downstream Products

98909-91-2Relevant academic research and scientific papers

METHOD FOR PRODUCING CARBONYL COMPOUND AN PRO-OXIDANT USED FOR PRODUCTION OF CARBONYL COMPOUND

-

Page/Page column 13; 14-15, (2009/08/16)

The invention provides a process for the preparation of a carbonyl compound in high efficiency by oxidizing an alcohol. The process for the preparation of a carbonyl compound of the present invention includes a step of oxidizing an alcohol in the presence of a compound of the formula (I) or a derivative or a salt thereof, and an oxidant, wherein R1 and R2 independently represent hydrogen, a halogen, a nitro or acidic group, or an alkyl or alkoxy group, each of which optionally has a substituent, or R1 and R2 combine the two carbon atoms to which they are boned to form an aromatic ring.

Addition of Aldehydes to Activated Double Bonds, XXXVI. Syntheses and Reactions of 3-Acyl-1,5-dicarbonyl Compounds

Stetter, Hermann,Simons, Leo

, p. 3172 - 3187 (2007/10/02)

Thiazolium salt-catalyzed addition of aldehydes to the 2-methylene-1,4-ketoketals 6-10 and to the unsaturated 2-(alkoxycarbonyl)-1,5-ketoketals 21-24 leads to 3-acyl-1,5-dicarbonyl compounds 30-41.Furthermore, the 4- and 5-(2-oxoalkyl)-2-cyclopenten-1-one

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