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2-Cyclopenten-1-one, 4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23033-96-7

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23033-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23033-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,3 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23033-96:
(7*2)+(6*3)+(5*0)+(4*3)+(3*3)+(2*9)+(1*6)=77
77 % 10 = 7
So 23033-96-7 is a valid CAS Registry Number.

23033-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-cyclopenten-1-one

1.2 Other means of identification

Product number -
Other names 4-methylcyclopent-2-en-1-one

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:23033-96-7 SDS

23033-96-7Upstream product

23033-96-7Relevant academic research and scientific papers

Thermal decomposition of ascorbic acid

Vernin, Gaston,Chakib, Soundouss,Rogacheva, Sonia M.,Obretenov, Tzvetan D.,Parkanyi, Cyril

, p. 1 - 15 (1997)

Thermal degradation of L-ascorbic acid at 300 °C in the absence of a solvent yielded mostly furan derivatives and α,β-unsaturated cyclic ketones with a five-membered ring. Some of the furan derivatives are the same as those obtained in the Maillard reaction, with the reductones undergoing retroaldol reaction, decarboxylation, oxidation, and hydrolysis. In propylene glycol, under milder conditions (180 °C), the carbonyl and dicarbonyl derivatives resulting from the decomposition react with the solvent and give cyclic acetals and ketals (1,3-dioxolanes). The products were identified by GC-MS using the SPECMA data bank.

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