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115062-74-3

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115062-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115062-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,0,6 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 115062-74:
(8*1)+(7*1)+(6*5)+(5*0)+(4*6)+(3*2)+(2*7)+(1*4)=93
93 % 10 = 3
So 115062-74-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H12N2O2/c1-9-5-3-6-10(2)13(9)17-14(18)11-7-4-8-16-12(11)15(17)19/h3-8H,1-2H3

115062-74-3SDS

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 6-(2,6-dimethylphenyl)pyrrolo[3,4-b]pyridine-5,7-dione

1.2 Other means of identification

Product number -
Other names DP-2,3-Pdc

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:115062-74-3 SDS

115062-74-3Downstream Products

115062-74-3Relevant articles and documents

Novel and versatile methodology for synthesis of cyclic imides and evaluation of their cytotoxic, DNA binding, apoptotic inducing activities and molecular modeling study

Abdel-Aziz, Alaa A.-M.

, p. 614 - 626 (2008/02/10)

Versatile method has been developed for synthesis of N-substituted imides. Thus, acid anhydrides, imides and dicarboxylic acids were successfully subjected to dehydrative cyclization with substituted amines using DPPOx and Et3N to afford N-substituted imides under mild conditions. The DNA binding and apoptosis induction were investigated with regard to their potential utility as cytotoxic agents. Molecular modeling methods are used to study the cytotoxic activity of the active compounds by means of molecular and quantum mechanics.

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