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100961-91-9

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100961-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100961-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,6 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100961-91:
(8*1)+(7*0)+(6*0)+(5*9)+(4*6)+(3*1)+(2*9)+(1*1)=99
99 % 10 = 9
So 100961-91-9 is a valid CAS Registry Number.

100961-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-dicyano-N-methyldiphenylamine

1.2 Other means of identification

Product number -
Other names N,N-bis(4-cyanophenyl)methylamine

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:100961-91-9 SDS

100961-91-9Downstream Products

100961-91-9Relevant articles and documents

Highly blue luminescent triazine-amine conjugated oligomers

Murase, Takashi,Fujita, Makoto

, p. 9269 - 9278 (2005)

The novel synthetic strategy and optical properties of highly fluorescent, triazine-amine conjugated oligomers are described herein. Under basic conditions, aromatic dinitrile compounds, NC-C6H4-X-C 6H4-CN (X =

Optimization of the central linker of dicationic bis-benzimidazole anti-MRSA and anti-VRE agents

Hu, Laixing,Kully, Maureen L.,Boykin, David W.,Abood, Norman

scheme or table, p. 3374 - 3377 (2010/02/28)

A series of bis-benzimidazole diamidine compounds containing different central linkers has been synthesized and evaluated for in vitro antibacterial activities, including drug-resistant bacterial strains. Seven compounds have shown potent antibacterial activities. The anti-MRSA and anti-VRE activities of compound 1h were more potent than that of the lead compound 1a and vancomycin.

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