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2-Butanone, 1,1,1,4,4,4-hexafluoro-3,3-bis(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88995-83-9

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88995-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88995-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,9 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88995-83:
(7*8)+(6*8)+(5*9)+(4*9)+(3*5)+(2*8)+(1*3)=219
219 % 10 = 9
So 88995-83-9 is a valid CAS Registry Number.

88995-83-9SDS

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 1,1,1,4,4,4-hexafluoro-3,3-bis(trifluoromethyl)butan-2-one

1.2 Other means of identification

Product number -
Other names 2-Butanone,1,1,1,4,4,4-hexafluoro-3,3-bis(trifluoromethyl)

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:88995-83-9 SDS

88995-83-9Downstream Products

88995-83-9Relevant academic research and scientific papers

The Reaction of Trifluoromethyl Radicals with Neopentane. An SH2 Reaction at a Saturated Aliphatic Carbon Atom

Jackson, Richard A,Townson, Michael

, p. 1452 - 1456 (2007/10/02)

When hexafluoroacetone is photolysed in the presence of neopentane at 300 deg C, isobutane is formed as a primary product, and 1,1,1-trifluoroethane is formed in amounts much greater than would be expected from combination of methyl and trifluoromethyl radicals.These results strongly support the occurence of a homolytic bimolecular substitution reaction (SH2) by a trifluoromethyl radical at a methyl carbon atom, with the displacement of a t-butyl radical.

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