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2-Phenazinamine, N,5-bis(4-chlorophenyl)-3,5-dihydro-3-[[2-(1-piperazinyl)ethyl]imino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111435-92-8

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111435-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111435-92-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,3 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111435-92:
(8*1)+(7*1)+(6*1)+(5*4)+(4*3)+(3*5)+(2*9)+(1*2)=88
88 % 10 = 8
So 111435-92-8 is a valid CAS Registry Number.

111435-92-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(4-chloro-anilino)-10-(4-chloro-phenyl)-10H-phenazin-2-ylidene]-(2-piperazin-1-yl-ethyl)-amine

1.2 Other means of identification

Product number -
Other names (4-Chloro-phenyl)-{5-(4-chloro-phenyl)-3-[(Z)-2-piperazin-1-yl-ethylimino]-3,5-dihydro-phenazin-2-yl}-amine

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:111435-92-8 SDS

111435-92-8Downstream Products

111435-92-8Relevant academic research and scientific papers

Antitubercular agents. Part 1: Synthesis of phthalimido- and naphthalimido-linked phenazines as new prototype antitubercular agents

Kamal, Ahmed,Babu, A. Hari,Ramana, A. Venkata,Sinha, Rakesh,Yadav,Arora, Sudarshan K.

, p. 1923 - 1926 (2007/10/03)

The preparation and antitubercular properties of a series of phthalimido- and naphthalimido-linked phenazines are described. Some of these new compounds inhibited the growth of Mycobacterium tuberculosis ATCC 27294, Mycobacterium avium ATCC 49601, Mycobacterium intracellulare ATCC 13950 and some clinical isolates.

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