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26944-42-3

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26944-42-3 Usage

Physical state

Colorless, clear liquid

Odor

Strong

Uses

a. Solvent
b. Intermediate in the production of various chemicals and pharmaceuticals

Boiling point

High

Water solubility

Low

Applications

a. Reaction chemistry
b. Organic synthesis

Stability

a. High thermal stability
b. High chemical stability

Suitability

a. High-temperature processes
b. Harsh chemical environments

Potential use

Building block for the synthesis of complex organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 26944-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,4 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26944-42:
(7*2)+(6*6)+(5*9)+(4*4)+(3*4)+(2*4)+(1*2)=133
133 % 10 = 3
So 26944-42-3 is a valid CAS Registry Number.

26944-42-3SDS

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 1,1,1-trifluorotetradecan-2-one

1.2 Other means of identification

Product number -
Other names 1,1,1,-trifluorotetradecan-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:26944-42-3 SDS

26944-42-3Relevant articles and documents

An efficient and expeditious synthesis of funcionalized trifluoromethyl ketones through lithium-iodine exchange reaction

Villuendas, Isabel,Parrilla, Alfredo,Guerrero, Angel

, p. 12673 - 12684 (1994)

A straightforward and very efficient synthesis of unsaturated long-chain trifluoromethyl ketones is achieved by metallation of the corresponding iodides in the presence of an equimolecular amount of tert-butyllithium, followed by reaction with a fluoroacylating agent.Metallation occurs quantitatively at -78 deg C and, in contrast to what has been generally recommended, there is no need to add the second equivalent of base, since its presence may be detrimental if other electrophilic functions are present in the molecule.

A new, practical and efficient sulfone-mediated synthesis of trifluoromethyl ketones from alkyl and alkenyl bromides

Mu?oz, Lourdes,Rosa, Esmeralda,Bosch, Ma. Pilar,Guerrero, Angel

, p. 3311 - 3313 (2007/10/03)

We report herein a new and efficient method to prepare trifluoromethyl ketones from the corresponding bromides through sulfones in good yields.

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