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78473-00-4

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78473-00-4 Usage

Chemical Properties

white powder

Check Digit Verification of cas no

The CAS Registry Mumber 78473-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,7 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78473-00:
(7*7)+(6*8)+(5*4)+(4*7)+(3*3)+(2*0)+(1*0)=154
154 % 10 = 4
So 78473-00-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Cl2N2/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2H,11H2

78473-00-4 Well-known Company Product Price

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  • Alfa Aesar

  • (A11269)  4-Amino-3,5-dichlorobenzonitrile, 97%   

  • 78473-00-4

  • 1g

  • 574.0CNY

  • Detail
  • Alfa Aesar

  • (A11269)  4-Amino-3,5-dichlorobenzonitrile, 97%   

  • 78473-00-4

  • 5g

  • 2157.0CNY

  • Detail
  • Alfa Aesar

  • (A11269)  4-Amino-3,5-dichlorobenzonitrile, 97%   

  • 78473-00-4

  • 25g

  • 10681.0CNY

  • Detail

78473-00-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-3,5-dichlorobenzonitrile

1.2 Other means of identification

Product number -
Other names 4-Cyano-2,6-dichloroaniline

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:78473-00-4 SDS

78473-00-4Relevant articles and documents

A practical and cost-efficient, one-pot conversion of aldehydes into nitriles mediated by 'activated DMSO'

Augustine, John Kallikat,Bombrun, Agnes,Atta, Rajendra Nath

, p. 2223 - 2227 (2011/10/31)

Participation of activated DMSO in the one-pot transformation of aldehydes to nitriles has been described by reacting aldehydes with NHHHCl in DMSO in the absence of any added base or catalyst. The method is applicable to access a wide range of aromatic, heterocyclic, and aliphatic nitriles, in which only water is a byproduct. A straightforward and practical procedure is demonstrated on a multigram scale. Georg Thieme Verlag Stuttgart - New York.

USE OF 2-[(3,5-DIHALO-4-AMINOBENZYL)] IMIDAZOLINES TO STIMULATE ALPHA-1 ADRENERGIC RECEPTORS AND TO TREAT NASAL CONGESTION

-

, (2008/06/13)

Disclosed herein are alpha adrenergic and nasal decongestant compounds of the formula STR1 wherein R 1 and R 2, each being the same or different, are halogens, and the pharmaceutically acceptable salts thereof.

Method for lowering intraocular pressure using phenylimino-imidazoles

-

, (2008/06/13)

2-(Trisubstituted phenylimino)-imidazole compounds also known as 2-(trisubstituted anilino)-1,3 diazacyclopentene-(2) compounds are used to lower intraocular pressure.

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