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1,4-Pentanediamine,N4-[10-(4-chlorophenyl)-3-[(4-chlorophenyl)amino]-2(10H)-phenazinylidene]-N1,N1-diethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111436-11-4

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111436-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111436-11-4 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 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111436-11:
(8*1)+(7*1)+(6*1)+(5*4)+(4*3)+(3*6)+(2*1)+(1*1)=74
74 % 10 = 4
So 111436-11-4 is a valid CAS Registry Number.

111436-11-4SDS

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-chloroanilino)-10-(4-chlorophenyl)-2-<<4-(diethylamino)-1-methylbutyl>imino>-2,10-dihydrophenazine

1.2 Other means of identification

Product number -
Other names N4-[10-(4-Chloro-phenyl)-3-(4-chloro-phenylamino)-10H-phenazin-(2E)-ylidene]-N1,N1-diethyl-pentane-1,4-diamine

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:111436-11-4 SDS

111436-11-4Downstream Products

111436-11-4Relevant academic research and scientific papers

Clofazimine Analogues Active against a Clofazimine-Resistant Organism

O'Sullivan, John F.,Conalty, Michael L.,Morrison, Norman E.

, p. 567 - 572 (2007/10/02)

Clofazimine analogues active against a strain of Mycobacterium smegmatis 607 made resistant to the antileprosy agent have been synthesized.Activity (i.e., /= 2 μg/mL causing complete inhibition of growth) requires that there be a basic nitrogen in the "rimino" side chain and that the spacer distance between this nitrogen and the imino nitrogen be at least three carbon atoms.The nitrogen may be primary, secondary, or tertiary and may be part of an open chain or enclosed in a ring compound.Provided that the criteria of basicity and spacer distance are satisfied, all are active in vitro against both the sensitive and resistant strains.Substitution elswhere in the molecule had little effect on the activity.The compounds have been shown to have growth inhibitory activity against human-derived Mycobacterium leprae in murine macrophages in culture.

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