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3-(4-Fluorophenyl)-1,1,1-trifluoro-2-propanone, also known as α-fluorotoluene trifluoromethyl ketone, is a synthetic organic compound characterized by its molecular formula C10H7F4O. This colorless liquid is a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is derived from the reaction of 4-fluorophenylmagnesium bromide with trifluoroacetone, showcasing its importance in fluorochemical synthesis. Due to its reactivity and unique properties, it is widely used in the preparation of fluorinated compounds, which have applications in various industries, including medicine, materials science, and chemical research.

1735-92-8

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1735-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1735-92-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1735-92:
(6*1)+(5*7)+(4*3)+(3*5)+(2*9)+(1*2)=88
88 % 10 = 8
So 1735-92-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F4O/c10-7-3-1-6(2-4-7)5-8(14)9(11,12)13/h1-4H,5H2

1735-92-8SDS

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-trifluoro-3-(4-fluorophenyl)propan-2-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:1735-92-8 SDS

1735-92-8Downstream Products

1735-92-8Relevant academic research and scientific papers

Highly efficient synthesis of chiral α-CF3 amines via Rh-catalyzed asymmetric hydrogenation

Jiang, Jun,Lu, Wenxin,Lv, Hui,Zhang, Xumu

, p. 1154 - 1156 (2015)

Highly enantioselective catalytic asymmetric hydrogenation of α-CF3-enamides has been achieved by employing rhodium-DuanPhos as the catalyst, which provides a readily accessible method for the synthesis of chiral trifluoromethylated amines. The reaction has a broad substrate scope; both aryl- and alkyl-substituted α-CF3-enamides worked smoothly and afford the corresponding chiral amines in high yields and excellent enantioselectivities (up to 99% ee).

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