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166312-68-1

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166312-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 166312-68-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,3,1 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 166312-68:
(8*1)+(7*6)+(6*6)+(5*3)+(4*1)+(3*2)+(2*6)+(1*8)=131
131 % 10 = 1
So 166312-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H13F3O3/c1-2-19-12(18)7-6-11(17)9-4-3-5-10(8-9)13(14,15)16/h3-5,8H,2,6-7H2,1H3

166312-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-oxo-4-[3-(trifluoromethyl)phenyl]butanoate

1.2 Other means of identification

Product number -
Other names ETHYL 4-OXO-4-(3-TRIFLUOROMETHYLPHENYL)BUTYRATE

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:166312-68-1 SDS

166312-68-1Downstream Products

166312-68-1Relevant articles and documents

A process for preparing γ - ketone carbonyl compounds

-

Paragraph 0150; 0151; 0152, (2018/07/30)

The present invention discloses a gamma-ketone carbonyl compound preparation method, wherein in the presence of an oxidizing agent, a styrene compound and ethyl diazoacetate are adopted as reactants, copper or a copper compound is adopted as a catalyst, DABCO is adopted as an alkali, and a free radical reaction is performed in a polar solvent isopropyl alcohol to obtain the product gamma-ketone carbonyl compound. According to the method of the present invention, the reaction activity of the catalyst is high, the reaction conditions are mild, the substrate application range is wide, the post-treatment is convenient, the yield of the target product is high, the preparation process is simple, and the sources of the used raw materials are wide.

Tris(4-methoxylphenyl)phosphine-catalyzed C-C bond formation reaction: Mutual addition of aromatic aldehydes and ethyl acrylate

Teng, Jun-Jiang,Qiao, Yan-Hui,Zhang, Qing,Li, Chun-Hai,Huang, Min

, p. 848 - 858 (2013/02/25)

A highly efficient intermolecular mutual addition of aromatic aldehydes with ethyl acrylate was developed by using tris(4-methoxylphenyl)phosphine as the catalyst. The reaction corresponds to the construction of 1,4-dicarbonyl compound and allylic alcohol

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