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356-27-4

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356-27-4 Usage

Chemical Properties

Clear colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 356-27-4 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 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 356-27:
(5*3)+(4*5)+(3*6)+(2*2)+(1*7)=64
64 % 10 = 4
So 356-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H5F7O2/c1-2-15-3(14)4(7,8)5(9,10)6(11,12)13/h2H2,1H3

356-27-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (H0594)  Ethyl Heptafluorobutyrate  >97.0%(GC)

  • 356-27-4

  • 5g

  • 230.00CNY

  • Detail
  • TCI America

  • (H0594)  Ethyl Heptafluorobutyrate  >97.0%(GC)

  • 356-27-4

  • 25g

  • 670.00CNY

  • Detail
  • Alfa Aesar

  • (A16742)  Ethyl heptafluorobutyrate, 98%   

  • 356-27-4

  • 25g

  • 605.0CNY

  • Detail
  • Alfa Aesar

  • (A16742)  Ethyl heptafluorobutyrate, 98%   

  • 356-27-4

  • 100g

  • 1781.0CNY

  • Detail

356-27-4SDS

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 ethyl 2,2,3,3,4,4,4-heptafluorobutanoate

1.2 Other means of identification

Product number -
Other names Ethyl heptafluorobutanoate

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:356-27-4 SDS

356-27-4Relevant articles and documents

Synthesis and studies of nucleophilic reactions of vicinal bis(fluorosulfonyloxy)perfluoroisononanes

Avetisyan,Cherstkov,Tumanskii,Sterlin

, p. 2429 - 2433 (2007/10/03)

The addition of peroxydisulfuryl difluoride (FSO3)2 to isomeric perfluoroisononenes (perfluoropropylene trimers) was studied. Isomers containing the trisubstituted C=C bond form adducts which were converted to the corresponding ketofluorosulfates under the action of weak nucleophiles (DMF and AcONa/AcOH) and underwent haloform-type decomposition under the action of CsF to form perfluoroalkenyl fluorosulfates and products of their subsequent conversions.

PERFLUOROCARBOXYLIC ACID ANHYDRIDES AND HALIDES IN THE WITTING REACTION

Volkonskii, A. Yu.,Mysov, E. I.,Rokhlin, E. M.

, p. 1246 - 1257 (2007/10/02)

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