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2,5-Pyrrolidinedione, 3-(2-nitrophenyl)-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112616-40-7

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112616-40-7 Usage

Chemical structure

Consists of a pyrrolidinedione ring with a 3-(2-nitrophenyl)-1-(phenylmethyl) side chain

Classification

Heterocyclic compound (lactam)

Uses

Building block in the synthesis of pharmaceuticals and other organic compounds

Functional groups

Nitro and phenyl groups in side chain

Versatility

Allows for introduction of diverse functional groups and modifications to structure

Applications

Medicinal chemistry, agrochemicals, material science

Check Digit Verification of cas no

The CAS Registry Mumber 112616-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,1 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112616-40:
(8*1)+(7*1)+(6*2)+(5*6)+(4*1)+(3*6)+(2*4)+(1*0)=87
87 % 10 = 7
So 112616-40-7 is a valid CAS Registry Number.

112616-40-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-3-(2-nitrophenyl)pyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names 2,5-Pyrrolidinedione,3-(2-nitrophenyl)-1-(phenylmethyl)

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:112616-40-7 SDS

112616-40-7Relevant academic research and scientific papers

STEREOCONTROLLED FORMATION OF 1,2-DIHYDROINDOLES

Veenstra, S.J.,Fortgens, H.P.,Vijn, R.J.,Jong, B.S. de,Speckamp, W.N.

, p. 1147 - 1156 (2007/10/02)

Imines 4 cyclize stereoselectively to dihydroindoles 2 upon use of a Li or Na alkoxide-alcohol combination.Depending on the type of alcohol applied either cis (2C) or trans (2T) spiroindolines 2 are formed.In case of imines 4 derived from electron-rich ar

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