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4-{[(Z)-(3-chloro-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]amino}benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71937-06-9

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71937-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71937-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,3 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71937-06:
(7*7)+(6*1)+(5*9)+(4*3)+(3*7)+(2*0)+(1*6)=139
139 % 10 = 9
So 71937-06-9 is a valid CAS Registry Number.

71937-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-{[(Z)-(3-Chloro-6-oxo-2,4-cyclohexadien-1-ylidene)methyl]amino} benzoic acid

1.2 Other means of identification

Product number -
Other names 6-(4-arsono-phenyl)-hexanoic acid

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:71937-06-9 SDS

71937-06-9Downstream Products

71937-06-9Relevant academic research and scientific papers

A ratiometric fluorescent pH probe based on aggregation-induced emission enhancement and its application in live-cell imaging

Song, Panshu,Chen, Xiaotong,Xiang, Yu,Huang, Lei,Zhou, Zhaojuan,Wei, Ruirui,Tong, Aijun

, p. 13470 - 13475 (2011)

A ratiometric fluorescent pH probe, 4-carboxylaniline-5- chlorosalicylaldehyde Schiff base (1) was synthesized via a facile reaction and used for pH sensing in live cells. While exhibiting weak fluorescence when dispersed in solution, 1 displayed aggregat

4-aminobenzoic acid derivatives: Converting folate precursor to antimicrobial and cytotoxic agents

Brablíková, Michaela,Jan?ourek, Ond?ej,Janou?ek, Ji?í,Kone?ná, Klára,Krátky, Martin,Stola?íková, Ji?ina,Trejtnar, Franti?ek,Vin?ová, Jarmila

, (2020/01/25)

4-aminobenzoic acid (PABA), an essential nutrient for many human pathogens, but dispensable for humans, and its derivatives have exhibited various biological activities. In this study, we combined two pharmacophores using a molecular hybridization approach: this vitamin-like molecule and various aromatic aldehydes, including salicylaldehydes and 5-nitrofurfural, via imine bond in one-step reaction. Resulting Schiff bases were screened as potential antimicrobial and cytotoxic agents. The simple chemical modification of non-toxic PABA resulted in constitution of antibacterial activity including inhibition of methicillin-resistant Staphylococcus aureus (minimum inhibitory concentrations, MIC, from 15.62 μM), moderate antimycobacterial activity (MIC ≥ 62.5 μM) and potent broad-spectrum antifungal properties (MIC of ≥ 7.81 μM). Some of the Schiff bases also exhibited notable cytotoxicity for cancer HepG2 cell line (IC50 ≥ 15.0 μM). Regarding aldehyde used for the derivatization of PABA, it is possible to tune up the particular activities and obtain derivatives with promising bioactivities.

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