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383-67-5

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383-67-5 Usage

Description

ALLYL TRIFLUOROACETATE is a clear, colorless liquid that serves as a nucleophilic ally metal precursor in alkylation reactions, which generate homoallylic amines. It is also utilized as a chemical reagent and intermediate in the pharmaceutical industry.

Uses

Used in Pharmaceutical Industry:
ALLYL TRIFLUOROACETATE is used as a chemical reagent and intermediate for the synthesis of various pharmaceutical compounds. Its role in alkylation reactions that produce homoallylic amines makes it a valuable component in the development of new drugs and medications.
Used in Chemical Synthesis:
As a nucleophilic ally metal precursor, ALLYL TRIFLUOROACETATE is employed in alkylation reactions, which are essential for the synthesis of a wide range of chemical compounds. This application is crucial in the development of new materials and products across various industries, including pharmaceuticals, agrochemicals, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 383-67-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 383-67:
(5*3)+(4*8)+(3*3)+(2*6)+(1*7)=75
75 % 10 = 5
So 383-67-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H5F3O2/c1-2-3-10-4(9)5(6,7)8/h2H,1,3H2

383-67-5 Well-known Company Product Price

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

  • (A11690)  Allyl trifluoroacetate, 97%   

  • 383-67-5

  • 10g

  • 372.0CNY

  • Detail
  • Alfa Aesar

  • (A11690)  Allyl trifluoroacetate, 97%   

  • 383-67-5

  • 50g

  • 1350.0CNY

  • Detail
  • Alfa Aesar

  • (A11690)  Allyl trifluoroacetate, 97%   

  • 383-67-5

  • 250g

  • 5130.0CNY

  • Detail
  • Aldrich

  • (374075)  Allyltrifluoroacetate  98%

  • 383-67-5

  • 374075-25G

  • 1,270.62CNY

  • Detail

383-67-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Allyltrifluoroacetate

1.2 Other means of identification

Product number -
Other names Acetic acid, trifluoro-, 2-propenyl ester

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:383-67-5 SDS

383-67-5Relevant articles and documents

-

Hoffmann,H.M.R. et al.

, p. 2257 - 2261 (1971)

-

Ortho-Phenylene bridged palladium bis-N-heterocyclic carbene complexes: Synthesis, structure and catalysis

Munz, Dominik,Poethig, Alexander,Tronnier, Alexander,Strassner, Thomas

, p. 7297 - 7304 (2013/07/11)

A series of ortho-phenylene bridged palladium bis-NHC complexes has been synthesized. Complexes with imidazolium and benzimidazolium derived NHCs and methyl-/benzyl-wingtips are reported. Bis(benz)imidazoles with a doubly brominated ortho-phenylene bridge could be obtained by an electrophilic substitution reaction. The structure of the complexes could be confirmed by three solid-state structures. All catalysts have been tested in the catalytic functionalisation of propane. The catalytic activity is highly dependent on the ligand, whereas ligand effects on the regioselectivity (n/iso) are much smaller.

Synthesis of bicyclo[2.2.1]hept-5-enyl methyl esters of haloacetic acids

Kyazimova,Mamedbeili,Nagiev,Suleimanova,Khalilov

experimental part, p. 1803 - 1807 (2009/09/08)

Synthesis of norbornenyl methyl esters of a number of haloacetic acids via [4+2] cycloaddition of cyclopentadiene to allyl esters of these acids was examined. The yield and isomer composition of the synthesized compounds were examined in relation to the reaction conditions, and the best conditions for their preparation were found.

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