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914225-70-0

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914225-70-0 Usage

Notes

Light Sensitive. Incompatible with light and oxidizing agents.

Uses

5'-Fluoro-2'-iodoacetophenone is used as pharmaceutical intermediates.

Materials Uses

1-(5-Fluoro-2-iodophenyl)ethanone is a reactant in the preparation of PF-06463922, a potent macrocyclic ALK inhibitor as potential antitumor.

Check Digit Verification of cas no

The CAS Registry Mumber 914225-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,2,2 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 914225-70:
(8*9)+(7*1)+(6*4)+(5*2)+(4*2)+(3*5)+(2*7)+(1*0)=150
150 % 10 = 0
So 914225-70-0 is a valid CAS Registry Number.

914225-70-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H66475)  5'-Fluoro-2'-iodoacetophenone, 97%   

  • 914225-70-0

  • 250mg

  • 336.0CNY

  • Detail
  • Alfa Aesar

  • (H66475)  5'-Fluoro-2'-iodoacetophenone, 97%   

  • 914225-70-0

  • 1g

  • 1008.0CNY

  • Detail
  • Alfa Aesar

  • (H66475)  5'-Fluoro-2'-iodoacetophenone, 97%   

  • 914225-70-0

  • 5g

  • 4032.0CNY

  • Detail

914225-70-0SDS

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 1-(5-Fluoro-2-iodophenyl)ethanone

1.2 Other means of identification

Product number -
Other names TD1027

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:914225-70-0 SDS

914225-70-0Relevant articles and documents

Preparation method of lorlatinib intermediate compound

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Paragraph 0033; 0037-0042; 0043; 0046-0047, (2020/04/06)

The invention relates to a preparation method of a lorlatinib intermediate compound. 4-fluoroacetanilide is taken as a raw material and carry out visible light Fries rearrangement in the presence of avisible light catalyst and visible light to obtain an i

Preparation method of 1-(5-fluoro-2-iodophenyl)ethanone

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Paragraph 0024; 0030; 0034, (2017/03/17)

The invention relates to a preparation method of 1-(5-fluoro-2-iodophenyl)ethanone.According to the method, 2-amino-5-fluorobenzoic acid and 5-fluoro-2-iodobenzoic acid react to prepare the final product 1-(5-fluoro-2-iodophenyl)ethanone.The method is sim

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