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359-61-5

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359-61-5 Usage

General Description

1,1,1-Trifluoro-3,3-dimethyl-butan-2-one is a chemical compound with the molecular formula C6H9F3O. It is a colorless liquid with a fruity odor and is commonly used as a solvent in various industrial processes. 1,1,1-TRIFLUORO-3,3-DIMETHYL-BUTAN-2-ONE is also used as an intermediate in the production of pharmaceuticals and agrochemicals. 1,1,1-Trifluoro-3,3-dimethyl-butan-2-one is known for its high solvency power, low boiling point, and good stability, making it a versatile chemical in different applications. However, it is important to handle this compound with care due to its potential health hazards and environmental impacts.

Check Digit Verification of cas no

The CAS Registry Mumber 359-61-5 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 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 359-61:
(5*3)+(4*5)+(3*9)+(2*6)+(1*1)=75
75 % 10 = 5
So 359-61-5 is a valid CAS Registry Number.

359-61-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-trifluoro-3,3-dimethylbutan-2-one

1.2 Other means of identification

Product number -
Other names 1,1,1-trifluoro-3,3-dimethyl-butan-2-one

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:359-61-5 SDS

359-61-5Downstream Products

359-61-5Relevant articles and documents

Direct preparation of trifluoromethyl ketones from carboxylic esters: Trifluoromethylation with (trifluoromethyl)trimethylsilane

Wiedemann, Juergen,Heiner, Thomas,Mloston, Gregorz,Prakash, G.K. Surya,Olah, George A.

, p. 820 - 821 (2007/10/03)

Previously difficult to prepare, alipathic and alicyclic trifluoromethylketones (e.g. 1 and 2), which are of pharmacologic interest as potential enzyme inhibitors, can now be synthesized easily and efficiently. The one-step reaction starting with carbonic esters and trimethyl(trifluoromethyl)silane is induced by tetrabutylammonium fluoride in nonpolar, aprotic solvents and proceeds without formation of double-addition products.

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