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1400691-55-5

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1400691-55-5 Usage

Uses

The Colby Trifluoromethylation Reagent is an air-stable, white solid, which can be used as a source of fluoroform through the release of trifluoroacetate. This reagent can add trifluoromethyl groups in a nucleophlic fashion to carbonyls and sulfides.

General Description

Colby trifluoromethylation reagent is an amidinate salt of hexafluoroacetone hydrate. This reagent can be prepared from the ethereal solution of hexafluoroacetone trihydrate. It undergoes various trifluoromethylation reactions with electrophiles under different reaction conditions to afford trifluoromethylated products.

Check Digit Verification of cas no

The CAS Registry Mumber 1400691-55-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,0,6,9 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1400691-55:
(9*1)+(8*4)+(7*0)+(6*0)+(5*6)+(4*9)+(3*1)+(2*5)+(1*5)=125
125 % 10 = 5
So 1400691-55-5 is a valid CAS Registry Number.

1400691-55-5 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (803774)  Colby trifluoromethylation reagent  

  • 1400691-55-5

  • 803774-1G

  • 497.25CNY

  • Detail
  • Aldrich

  • (803774)  Colby trifluoromethylation reagent  

  • 1400691-55-5

  • 803774-10G

  • 3,105.18CNY

  • Detail

1400691-55-5Relevant articles and documents

Amidinate salt of hexafluoroacetone hydrate for the preparation of fluorinated compounds by the release of trifluoroacetate

Riofski, Mark V.,Hart, Allison D.,Colby, David A.

supporting information, p. 208 - 211 (2013/04/10)

A powerful, new reagent, an amidinate salt of hexafluoroacetone hydrate, is an air-stable salt that can be used for the preparation of fluorinated organic molecules. Nucleophilic trifluoromethylation reactions are demonstrated following the base-promoted release of trifluoroacetate. This reagent is soluble in many polar organic solvents and produces fluoroform, following the release of trifluoroacetate. Reactions with this reagent and common electrophiles provide excellent yields of trifluoromethylated products.

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