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2-BROMO-4-CHLOROBENZONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 57381-49-4 Structure
  • Basic information

    1. Product Name: 2-BROMO-4-CHLOROBENZONITRILE
    2. Synonyms: 2-BROMO-4-CHLOROBENZONITRILE;2-bromo-4-chlorophenyl-carbonitrile
    3. CAS NO:57381-49-4
    4. Molecular Formula: C7H3BrClN
    5. Molecular Weight: 216.46242
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 57381-49-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 284.0±25.0℃ (760 Torr)
    3. Flash Point: 125.6±23.2℃
    4. Appearance: /
    5. Density: 1.74±0.1 g/cm3 (20 ºC 760 Torr)
    6. Vapor Pressure: 0.003mmHg at 25°C
    7. Refractive Index: 1.623
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-BROMO-4-CHLOROBENZONITRILE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-BROMO-4-CHLOROBENZONITRILE(57381-49-4)
    12. EPA Substance Registry System: 2-BROMO-4-CHLOROBENZONITRILE(57381-49-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 57381-49-4(Hazardous Substances Data)

57381-49-4 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 57381-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,8 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57381-49:
(7*5)+(6*7)+(5*3)+(4*8)+(3*1)+(2*4)+(1*9)=144
144 % 10 = 4
So 57381-49-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H3BrClN/c8-7-3-6(9)2-1-5(7)4-10/h1-3H

57381-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-4-chlorobenzonitrile

1.2 Other means of identification

Product number -
Other names 2-BROMO-4-CHLOROBENZONITRILE

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:57381-49-4 SDS

57381-49-4Relevant articles and documents

A radical cyclization cascade of 2-alkynylbenzonitriles with sodium arylsulfinates

Zhou, Bang,Chen, Wenqi,Yang, Yuzhong,Yang, Yuan,Deng, Guobo,Liang, Yun

, p. 7959 - 7963 (2018/11/21)

A convenient radical cyclization cascade procedure for the construction of sulfonated indenones from 2-alkynylbenzonitriles and sodium arylsulfinates has been explored under mild reaction conditions. The present methodology offers a low-cost and operationally straightforward approach to synthesizing various sulfonated indenones in moderate to good yields by simple use of cheap sodium persulfate as an oxidant and environmentally benign water as a co-solvent.

SUBSTITUTED QUINOLONES III

-

Page/Page column 9-10, (2009/07/25)

The invention relates to substituted quinolones and to methods for their preparation as well as to their use for the production of medicaments for the treatment and/or prophylaxis of diseases, especially for use as antiviral agents, particularly against cytomegaloviruses.

Synthesis of C-linked immobilized analogs of aloisine A by 'click' chemistry

Haddoub, Rose,Gueyrard, David,Goekjian, Peter G.

body text, p. 741 - 744 (2009/04/19)

An efficient approach for the immobilization of a series of analogs of aloisine A, an in vitro inhibitor of protein kinases, to polymeric supports via a [3+2] cycloaddition reaction is reported.

Substituted quinolones II

-

Page/Page column 9, (2008/12/04)

The invention relates to substituted quinolones of formula (I) and to methods for their preparation as well as their use for the production of medicaments for the treatment and/or prophylaxis of diseases, especially for use as antiviral agents, in particu

SUBSTITUTED QUINOLONES

-

Page/Page column 47-48, (2010/02/15)

The invention relates to substituted quinolones methods for production and use thereof for the production of medicaments for the treatment and/or prophylaxis of diseases, in particular, for use as antiviral agents, in particular, against cytomegaloviruses.

Simplified Synthesis of the Precursor for the Azo Dye Chlorindazone DS

Voss,Eichner

, p. 201 - 204 (2007/10/03)

Recently, Chlorindazone DS 1 has become an important analytical reagent for the detection of gunshot residues from newly introduced ammunition. A simplified synthesis of the precursor of the azo dye 1, 3-amino-6-chloroindazole (2), from commercially available 2,4-dichlorobenzonitrile (3a) has been described. The physical and spectroscopical properties of the known compounds 1 and 2 have been completed. 2-Chloro-4-hydrazinobenzonitrile (4a), 2-bromo-4-hydrazinobenzonitrile (4b) and a new azo dye, 1-(3′-chloro-4′-cyanobenzene-1′-ylazo)-2-hydroxynaphthalene-3, 6-disulfonic acid, disodium salt (5), have been investigated.

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