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354-76-7

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354-76-7 Usage

Uses

2,2,3,3,3-Pentafluoropropionamide, is used as a chemical, organic, pharamceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 354-76-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 354-76:
(5*3)+(4*5)+(3*4)+(2*7)+(1*6)=67
67 % 10 = 7
So 354-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H2F5NO/c4-2(5,1(9)10)3(6,7)8/h(H2,9,10)

354-76-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B21566)  2,2,3,3,3-Pentafluoropropionamide, 97%   

  • 354-76-7

  • 5g

  • 607.0CNY

  • Detail
  • Alfa Aesar

  • (B21566)  2,2,3,3,3-Pentafluoropropionamide, 97%   

  • 354-76-7

  • 25g

  • 2423.0CNY

  • Detail

354-76-7SDS

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 PENTAFLUOROPROPIONAMIDE

1.2 Other means of identification

Product number -
Other names pentafluoropropionic acid amide

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:354-76-7 SDS

354-76-7Relevant articles and documents

-

Hauptschein,M.,Braid,M.

, p. 2500 - 2505 (1961)

-

-

Husted,Ahlbrecht

, p. 1605,1607 (1953)

-

FLUOROALKYL-CONTAINING β,β'-TRICARBONYL COMPOUNDS: TAUTOMERISM AND REACTION WITH N-NUCLEOPHILES

Krokhalev, V. M.,Saloutin, V. I.,Romas', A. D.,Ershov, B. A.,Pashkevich, K. I.

, p. 316 - 322 (2007/10/02)

The tautomeric composition of α-polyfluoroacyl derivatives of acetylacetone and malonic ester has been established and it has been shown that with N-nucleophiles (ammonia, 1,2-ethylenediamine, o-phenylenediamine) these compounds undergo 'acid' decomposition with the elimination of the polyfluoroacyl group.With hydrazines, malonic ester derivatives react similarly but acetylacetone derivatives undergo cyclization into pyrazoles.The regiodirectivity of the interaction of fluoroalkyl-containing β,β'-tricarbonyl compounds with N-nucleophiles does not depend on their tautomeric composition and is determined by orbital control.

SYNTHESIS AND REACTIONS OF OXYGEN CONTAINING ORGANOFLUORINE COMPOUNDS. IX. REACTION OF POLYFLUOROALKYL KETONES WITH AMMONIA

Saloutina, L. V.,Zapevalov, A. Ya.,Kolenko, I. P.

, p. 2019 - 2024 (2007/10/02)

The reaction of polyfluoroalkyl ketones with ammonia at reduced temperature was studied.The products from addition of ammonia at the carbonyl group, i.e., geminal amino alkohols, were obtained.If there are chlorine and bromine atoms at the α position, the polyfluoroalkyl ketones dissociate under the influence of ammonia to carboxamides and polyhalogenoalkanes.

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