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37172-87-5

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37172-87-5 Usage

Chemical Class

Perfluorinated compound

Structure

Ketone derivative with a perfluorobutanoyl group attached to a cyclohexanone ring

Industrial Applications

Building block for specialty polymers, surfactants, and fluorinated coatings

Properties

Highly resistant to heat, chemical reactions, and environmental degradation

Environmental Concerns

Persistence in the environment and potential toxicity

Handling and Disposal

Proper handling, use, and disposal required to minimize potential risks.

Check Digit Verification of cas no

The CAS Registry Mumber 37172-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,7 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37172-87:
(7*3)+(6*7)+(5*1)+(4*7)+(3*2)+(2*8)+(1*7)=125
125 % 10 = 5
So 37172-87-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H9F7O2/c11-8(12,9(13,14)10(15,16)17)7(19)5-3-1-2-4-6(5)18/h5H,1-4H2

37172-87-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,2,3,3,4,4,4-heptafluorobutanoyl)cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-(2,2,3,3,4,4,4-heptafluorobutanoyl)cyclohexanone

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:37172-87-5 SDS

37172-87-5Downstream Products

37172-87-5Relevant articles and documents

Reaction of cycloalkylphosphorane with perfluoroalkylnitrile: A new synthesis of some fluorine-containing cyclic 1,3-diketones and oxo esters

Trabelsi,Cambon

, p. 315 - 319 (2007/10/02)

The preparation of some new perfluoroalkyl 1,3-dicarbonyl compounds is reported. The alcoholysis reaction of these 2-perfluoroalkanoylcycloalkanones in the presence or in the absence of base catalysis occurs, involving ring cleavage to yield fluorinated o

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