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3273-78-7

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3273-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3273-78-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,7 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3273-78:
(6*3)+(5*2)+(4*7)+(3*3)+(2*7)+(1*8)=87
87 % 10 = 7
So 3273-78-7 is a valid CAS Registry Number.

3273-78-7SDS

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-(4-amino-3-nitrophenoxy)-2-nitroaniline

1.2 Other means of identification

Product number -
Other names 3,3'-dinitro-4,4'-diaminodiphenyl ether

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:3273-78-7 SDS

3273-78-7Relevant articles and documents

Design of novel bis-benzimidazole derivatives as DNA minor groove binding agents

Wang, Xiu-Jun,Yang, Ming-Li,Zhang, Lan-Ping,Yao, Tong,Chen, Cheng,Mao, Lian-Gang,Wang, Yin,Wu, Jie

, p. 589 - 592 (2014/05/06)

A new series of bis-benzimidazole derivatives were designed and synthesized. In vitro cytotoxicity evaluation showed that these compounds exhibited high activity against the selected tumor cells. Among them, compound 9 owned the best potential, its IC50 values being 5.95 μmol/L (mononuclear tumor cell line (U937)) and 5.58 μmol/L (cervical cancer cell (HeLa)). Fluorescence and UV-vis studies showed that compound 9 could bind into the minor groove of DNA.

Oppi briefs practical and efficient synthesis of 4,4'-dihydroxy-3,3'- dinitrodiphenyl ether and 1,3-bis(4-hydroxy-3-nitrophenoxy)benzene in aqueous alkaline medium

Imoto, Mitsutaka,Takeda, Motonori,Tamaki, Akihiro,Taniguchi, Hisaji,Mizuno, Kazuhiko

scheme or table, p. 161 - 167 (2010/09/05)

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Synthesis and structure of Di[methoxy(ethoxy)carbonylamino-1H-benzimidazol- 5-yl] ethers

Pilyugin,Sapozhnikov,Kiseleva,Sapozhnikova,Vorob'eva,Klimakova

, p. 1509 - 1513 (2007/10/03)

A procedure was developed for preparing di[methoxy(ethoxy)carbonylamino-1H- benzimidazol-5-yl] ethers by the reaction of methyl or ethyl chloroformate with sodium cyanamide, followed by the reaction of the resulting methyl or ethyl cyanocarbamate with 4-(3,4-diaminophenoxy)-1,2-phenylenediamine in acidic solution. 2005 Pleiades Publishing, Inc.

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