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2,2-Pyrrolidinedicarboxylic acid, 1-(4-methylphenyl)-5-oxo-3-phenyl-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32285-86-2

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32285-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32285-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,8 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32285-86:
(7*3)+(6*2)+(5*2)+(4*8)+(3*5)+(2*8)+(1*6)=112
112 % 10 = 2
So 32285-86-2 is a valid CAS Registry Number.

32285-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-oxo-3-phenyl-1-p-tolyl-pyrrolidine-2,2-dicarboxylic acid diethyl ester

1.2 Other means of identification

Product number -
Other names 5-Oxo-3-phenyl-1-p-tolyl-pyrrolidine-2,2-dicarboxylic acid diethyl ester

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:32285-86-2 SDS

32285-86-2Relevant academic research and scientific papers

Chemoselective reduction of a lactam carbonyl group in the presence of a gem-dicarboxylate by sodium borohydride and iodine: A facile entry to N-aryl trisubstituted pyrroles

Haldar, Pranab,Ray, Jayanta K.

, p. 8229 - 8231 (2007/10/03)

Several N-aryl γ-lactam gem dicarboxylates were chemoselectively reduced to cyclic amine diesters by using sodium borohydride-iodine system. The reduction in all cases was completed within 2.5 h after refluxing in THF. The cyclic amine products were isolated after aqueous (acidic) workup in good yields. Hydrolytic decarboxylation followed by dehydrogenation produced N-aryl carboethoxy pyrroles.

SYNTHESIS OF SOME 9-ARYL-9-AZA-2,8-DIOXO-4,5-BENZOBICYCLONONANE, A NEW HETEROCYCLIC SYSTEM

Ghosh, Malay,Kar, Gandhi K. Ray, Jayanta K.,Chatterjee, Basanta G.

, p. 667 - 676 (2007/10/02)

A new and vaersatile synthetic procedure for the title compound is reported.Two routes for the cyclization of diazoketones (4) has been developed.

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