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141023-04-3

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141023-04-3 Usage

Synthesis Reference(s)

Tetrahedron, 51, p. 2573, 1995 DOI: 10.1016/0040-4020(95)00006-T

Check Digit Verification of cas no

The CAS Registry Mumber 141023-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,2 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 141023-04:
(8*1)+(7*4)+(6*1)+(5*0)+(4*2)+(3*3)+(2*0)+(1*4)=63
63 % 10 = 3
So 141023-04-3 is a valid CAS Registry Number.

141023-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-trifluorododec-11-en-2-one

1.2 Other means of identification

Product number -
Other names 1,1,1-TRIFLUORO-11-DODECENE-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:141023-04-3 SDS

141023-04-3Downstream Products

141023-04-3Relevant articles and documents

Chemoselective Trifluoromethylation of Methyl Esters Using an Et3GeNa/C6H5SCF3 Combination: Efficient Synthesis of Trifluoromethyl Ketones

Yokoyama, Yasuo,Mochida, Kunio

, p. 907 - 908 (1997)

Various trifluoromethyl ketones were synthesized from the corresponding methyl esters by effective nucleophilic trifluoromethylation using an Et3GeNa/C6H5SCF3 combination. This trifluoromethylation proceeded che

A new entry for the oxidation of fluoroalkyl-substituted methanol derivatives: Scope and limitation of the organoiodine(V) reagent-catalyzed oxidation

Tanaka, Yusuke,Ishihara, Takashi,Konno, Tsutomu

experimental part, p. 99 - 104 (2012/05/07)

Oxidation of various fluoroalkyl-substituted methanol derivatives under the influence of a catalytic amount of sodium 2-iodobenzenesulfonate and Oxone in CH3CN or CH3NO2 was investigated in detail. The efficiency of the newly developed oxidation was also evaluated by comparison to other oxidations, such as Dess-Martin, PDC, and Swern oxidation.

An expedient access to trifluoromethyl ketones from carboxylic acids

Boivin, Jean,El Kaim, Laurent,Zard, Samir Z.

, p. 1285 - 1288 (2007/10/02)

Trifluoromethyl ketones are prepared in good yield from carboxylic acid chlorides by reaction with pyridine and trifluoroacetic anhydride.

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