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359-61-5

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359-61-5 Usage

Physical state

Colorless liquid

Odor

Fruity

Common use

Solvent in various industrial processes

Application

Intermediate in the production of pharmaceuticals and agrochemicals

Solvency power

High

Boiling point

Low

Stability

Good

Versatility

Suitable for different applications

Health hazards

Potential health risks require careful handling

Environmental impact

Potential negative effects on the environment, necessitating careful handling and disposal

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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