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320-65-0

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320-65-0 Usage

Chemical Properties

clear light yellow liquid

Uses

2-Fluorobenzal Chloride is an important reagent in the synthesis of Benzenesulfonyl fluoride derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 320-65-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 320-65:
(5*3)+(4*2)+(3*0)+(2*6)+(1*5)=40
40 % 10 = 0
So 320-65-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Cl2F/c8-7(9)5-3-1-2-4-6(5)10/h1-4,7H

320-65-0 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (L03984)  2-Fluorobenzal chloride, 97%   

  • 320-65-0

  • 5g

  • 333.0CNY

  • Detail
  • Alfa Aesar

  • (L03984)  2-Fluorobenzal chloride, 97%   

  • 320-65-0

  • 25g

  • 1186.0CNY

  • Detail
  • Alfa Aesar

  • (L03984)  2-Fluorobenzal chloride, 97%   

  • 320-65-0

  • 100g

  • 3410.0CNY

  • Detail

320-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-FLUOROBENZAL CHLORIDE

1.2 Other means of identification

Product number -
Other names ortho-fluoro-benzal chloride

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:320-65-0 SDS

320-65-0Relevant articles and documents

A simple and efficient procedure for the preparation of benzal chlorides and benzal bromides

Léonel, Eric,Paugam, Jean-Paul,Heintz, Monique,Nédélec, Jean-Yves

, p. 4015 - 4024 (2007/10/03)

Benzal chlorides and benzal bromides were conveniently synthesized by reaction of aryl aldehydes with a Vilsmeier type reagent formed in situ by reduction of CCl4 or CBr4 in dimethylformamide (DMF) as solvent.

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