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3,3,4,4,4-PENTAFLUOROBUTENE-1 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

374-27-6

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374-27-6 Usage

Flammability and Explosibility

Flammable

Check Digit Verification of cas no

The CAS Registry Mumber 374-27-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 374-27:
(5*3)+(4*7)+(3*4)+(2*2)+(1*7)=66
66 % 10 = 6
So 374-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H3F5/c1-2-3(5,6)4(7,8)9/h2H,1H2

374-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,4,4,4-pentafluorobut-1-ene

1.2 Other means of identification

Product number -
Other names 3,3,4,4,4-pentafluorobutene

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:374-27-6 SDS

374-27-6Relevant academic research and scientific papers

Novel Fire Retardant Compounds

-

Paragraph 0062-0063, (2017/01/19)

Compounds with fire extinguishing properties having the formula: wherein R1 is —CR5R6R7 or —CR5R6CR8R9R10 as well as fire extinguishing units including one or more of the compounds.

Preparation, fluorination and synthetic utility of a CFC-olefin adduct

Van Der Puy, Michael,Demmin, Timothy R.,Bindu Madhavan,Thenappan, Alagappan,Tung, Harry S.

, p. 49 - 54 (2007/10/03)

1,1,1-Trichlorotrifluoroethane was added to ethylene using the catalyst system Fe/triethylphosphite, which eliminated the need for a solvent and avoided the corrosion problems inherent in CuCl-catalyzed reactions. The adduct, CF3CCl2CH2CH2Cl, was fluorinated with HF over a chromium(III) oxide catalyst. A series of alternating dehydrochlorinations and HF additions to internal C=C double bonds was proposed and supported by thermodynamic calculations to explain the formation of CF3CF2CH=CH2 as the principal fluorination product. An intermediate, CF3CCl=CHCH2Cl, formed cleanly by dehydrochlorination of the adduct in the absence of HF, was converted into 4,4,4-trifluorobutanol and other compounds of the type CF3CCl=CHCH2X (X =OAc, OH, Br, I, H).

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