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29553-26-2

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29553-26-2 Usage

General Description

2,2,3,3-Tetrafluoro-1,1-dimethylpropanol is a chemical compound with the molecular formula C5H9F4O. It is a colorless liquid with a boiling point of 70-72°C and a molecular weight of 160.11 g/mol. 2,2,3,3-TETRAFLUORO-1,1-DIMETHYLPROPANOL is used as a solvent, surfactant, and in the production of various industrial products. It is also known to be non-flammable and non-toxic, making it suitable for use in a wide range of applications. This chemical is an important intermediate in the production of fluorinated organic compounds and is used in the pharmaceutical and agrochemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 29553-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,5 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29553-26:
(7*2)+(6*9)+(5*5)+(4*5)+(3*3)+(2*2)+(1*6)=132
132 % 10 = 2
So 29553-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H8F4O/c1-4(2,10)5(8,9)3(6)7/h3,10H,1-2H3

29553-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,4,4-tetrafluoro-2-methylbutan-2-ol

1.2 Other means of identification

Product number -
Other names 3,3,4,4-Tetrafluor-2-methyl-butan-2-ol

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:29553-26-2 SDS

29553-26-2Relevant articles and documents

Promising prospects for using partially fluorinated alcohols as O-nucleophilic reagents in organofluoric synthesis

Il'in,Il'in,Bakhmutov,Furin,Pokrovskii

, p. 405 - 418 (2008/02/02)

Perfluoroolefins react with isopropyl alcohol under the conditions of radical initiation to form partially fluorinated aliphatic alcohols. The reactions of these alcohols with hexafluoropropylene and compounds containing labile halogen atoms (in particular, with allyl bromide and epichlorohydrin) were studied.

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