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756-09-2

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756-09-2 Usage

Uses

3H-Tetrafluoropropionic acid is used to produce 2,2,3,3-tetrafluoro-propionyl chloride. This reaction will need reagent benzotrichloride.

Check Digit Verification of cas no

The CAS Registry Mumber 756-09-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 756-09:
(5*7)+(4*5)+(3*6)+(2*0)+(1*9)=82
82 % 10 = 2
So 756-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H2F4O2/c4-1(5)3(6,7)2(8)9/h1H,(H,8,9)/p-1

756-09-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A19648)  3H-Tetrafluoropropionic acid, 97%   

  • 756-09-2

  • 2.5g

  • 442.0CNY

  • Detail
  • Alfa Aesar

  • (A19648)  3H-Tetrafluoropropionic acid, 97%   

  • 756-09-2

  • 10g

  • 1445.0CNY

  • Detail

756-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name flupropanate

1.2 Other means of identification

Product number -
Other names tetrapion

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:756-09-2 SDS

756-09-2Relevant articles and documents

PYRIMIDONE DERIVATIVES AS SELECTIVE CYTOTOXIC AGENTS AGAINST HIV INFECTED CELLS

-

Page/Page column 48, (2020/07/14)

The present disclosure is directed to pyrimidone derivatives of Formula I and their use for selectively killing HIV infected GAG-POL expressing cells without concomitant cytotoxicity to HIV nave cells, and for the treatment or prophylaxis of infection by HIV, or for the treatment, prophylaxis or delay in the onset or progression of AIDS or AIDS Related Complex (ARC).

Polyfluoroalkoxy phosphonic and phosphinic acid derivatives: II. Reversible esterase inhibitors

Krutikova,Krutikov,Erkin

experimental part, p. 434 - 439 (2010/08/04)

Polyfluoroalkyl esters of phosphoric, alkylphosphonic and 1-hydroxypolyfluoroalkylphosphonic acids exhibited significant antiesterase activity against various esterases of animal and microbial origin. Moreover, with some compounds reversible inhibition of enzymes was observed due to the specific influence of hydrophobic fragments of the target products.

Method for preparing α-substituted ω-hydroperfluoroalkanes

-

, (2008/06/13)

A method for the preparation of α-substituted ω-dihydroperluoroalkane derivatives of the general formula H(CF2 CF2)n R wherein R=H or COOH, and n=1-10 is characterized by oxidizing α, α, ω-trihydroperfluoroalcohols with an oxygen gas or an oxygen-containing gas in the presence of a homogeneous copper catalyst and an alkaline agent in an organic solvent with subsequent isolation of the desired product.

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