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2,5-Pyrrolidinedione, 1-[(2-bromophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115363-86-5

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115363-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115363-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,6 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115363-86:
(8*1)+(7*1)+(6*5)+(5*3)+(4*6)+(3*3)+(2*8)+(1*6)=115
115 % 10 = 5
So 115363-86-5 is a valid CAS Registry Number.

115363-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-bromobenzyl)pyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names N-(o-bromobenzyl)succinimide

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:115363-86-5 SDS

115363-86-5Relevant academic research and scientific papers

Design and optimization of tricyclic phtalimide analogues as novel inhibitors of HIV-1 integrase

Verschueren, Wim G.,Dierynck, Inge,Amssoms, Katie I. E.,Hu, Lili,Boonants, Paul M. J. G.,Pille, Geert M. E.,Daeyaert, Frits F. D.,Hertogs, Kurt,Surleraux, Dominique L. N. G.,Wigerinck, Piet B. T. P.

, p. 1930 - 1940 (2007/10/03)

Human immunodeficiency virus type-1 integrase is an essential enzyme for effective viral replication and hence a valid target for the design of inhibitors. We report here on the design and synthesis of a novel series of phthalimide analogues as integrase

Formation of Fused Tricyclic Azetidinones and Pyrrolidinones by Intramolecular SH2 Processes

Beckwith, A. L. J.,Boate, D. R.

, p. 4339 - 4348 (2007/10/02)

Treatment of a variety of suitably substituted sulfides of N-(o-halobenzyl)- or N-(o-halophenyl)azetidinone (e.g., 4 and 8) and -pyrrolidinone (e.g., 12 and 14) systems with either tributylstannane or tributyltin deuteride affords, by aryl radical substit

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