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1-Benzyl-2-methyl-3-pyrrolidone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69079-26-1

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69079-26-1 Usage

Chemical Properties

Orange Oil

Check Digit Verification of cas no

The CAS Registry Mumber 69079-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,7 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69079-26:
(7*6)+(6*9)+(5*0)+(4*7)+(3*9)+(2*2)+(1*6)=161
161 % 10 = 1
So 69079-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO/c1-10-12(14)7-8-13(10)9-11-5-3-2-4-6-11/h2-6,10H,7-9H2,1H3

69079-26-1SDS

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 1-benzyl-2-methylpyrrolidin-3-one

1.2 Other means of identification

Product number -
Other names 1-Benzyl-2-methyl-3-pyrrolidon

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:69079-26-1 SDS

69079-26-1Downstream Products

69079-26-1Relevant academic research and scientific papers

Heterocyclization of oximes of 3,5-dimethyl(1,3,5-trimethyl)-2,6- diphenylpiperid-4-ones and N-benzylpyrrolid-3-ones with acetylene in a superbasic medium

Voskressensky,Borisova,Varlamov

, p. 326 - 333 (2007/10/03)

It has been established that on heterocyclization of 3,5-dimethyl-2,6- diphenylpiperid-4-one oxime with acetylene in a superbasic medium migration of the 3a-CH3 group to the anionic nitrogen atom occurs, leading to the formation of 5,7-dimethyl-4,6-diphenyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridine. The formation of the N-anion causes aromatization of the tetrahydropyridine ring. Tetrahydropyrrolo-[1,2-c]pyrimidines are formed in the Trofimov reaction as a result of decomposition of the intermediate 3H-pyrrole in a retro-Mannich reaction.

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