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88134-15-0

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88134-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88134-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,3 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88134-15:
(7*8)+(6*8)+(5*1)+(4*3)+(3*4)+(2*1)+(1*5)=140
140 % 10 = 0
So 88134-15-0 is a valid CAS Registry Number.

88134-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-N-[2-[(2-nitrobenzoyl)amino]phenyl]benzamide

1.2 Other means of identification

Product number -
Other names -

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:88134-15-0 SDS

88134-15-0Relevant articles and documents

Regio- and stereoselectivity in preparation of benzene bridged bis- and tris-Troeger's bases

Valik, Martin,Dolensky, Bohumil,Petrickova, Hana,Kral, Vladimir

, p. 609 - 621 (2007/10/03)

Synthetic strategy for novel multiple Troeger's base derivatives is presented. Compounds were prepared in three steps: o-nitrobenzoylation of benzene-1,2- and -1,3-diamines 3 followed by reduction of nitro and amide groups to amino functions and treatment

Metal Template Reactions. XVI. Design and Synthesis of Primary Diamine Ligands with Additional Nitrogen Donor Atoms

Black, David St. C.,Rothnie, Neil E.

, p. 1141 - 1147 (2007/10/02)

Five new primary diamines (8), (10), (12), (20) and (22) have been synthesized.These compounds contain additional nitrogen donor atoms suitable for metal chelation.An improved preparation of the triamine (6) is also reported.

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