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94087-40-8

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94087-40-8 Usage

Chemical Properties

white to light yellow crystal powder

Check Digit Verification of cas no

The CAS Registry Mumber 94087-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,8 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 94087-40:
(7*9)+(6*4)+(5*0)+(4*8)+(3*7)+(2*4)+(1*0)=148
148 % 10 = 8
So 94087-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClFN/c9-7-3-1-2-6(4-5-11)8(7)10/h1-3H,4H2

94087-40-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H31443)  3-Chloro-2-fluorobenzonitrile, 97%   

  • 94087-40-8

  • 1g

  • 468.0CNY

  • Detail
  • Alfa Aesar

  • (H31443)  3-Chloro-2-fluorobenzonitrile, 97%   

  • 94087-40-8

  • 5g

  • 1991.0CNY

  • Detail

94087-40-8SDS

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 3-Chloro-2-fluorobenzonitrile

1.2 Other means of identification

Product number -
Other names 2-fluoro-3-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:94087-40-8 SDS

94087-40-8Upstream product

94087-40-8Relevant articles and documents

A 2-fluoro-3-chlorobenzene process for the preparation of formaldehyde

-

Paragraph 0025; 0026, (2017/03/08)

The invention relates to the field of fine chemical intermediates, in particular to a preparation method for 2-fluoro-3-chlorobenzaldehyde, namely, a fluorine-containing medical intermediate. According to the method, 2,3-dichlorobenzonitrile serves as raw materials, and 2-fluoro-3-chlorobenzaldehyde is obtained after fluorination, hydrolysis, oxidation and reduction are conducted. The method is low in raw material cost, high in apparent availability, mature and stable in reaction technology, high in operability and beneficial to industrial production.

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