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155628-02-7

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155628-02-7 Usage

General Description

Ethanone, 2,2,2-trifluoro-1-[3-(1-methylethyl)phenyl]- (9CI) is a chemical compound that consists of a trifluoromethyl group, a ketone group, and a phenyl group with an isopropyl substituent. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Ethanone, 2,2,2-trifluoro-1-[3-(1-methylethyl)phenyl]- (9CI) has potential uses in the field of organic chemistry for the development of new synthetic pathways and as a building block for the creation of more complex molecules. However, it is important to handle this chemical with care as it may have hazardous properties and should be used in a controlled environment with appropriate safety measures in place.

Check Digit Verification of cas no

The CAS Registry Mumber 155628-02-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,6,2 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 155628-02:
(8*1)+(7*5)+(6*5)+(5*6)+(4*2)+(3*8)+(2*0)+(1*2)=137
137 % 10 = 7
So 155628-02-7 is a valid CAS Registry Number.

155628-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-1-(3-propan-2-ylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 3'-iso-Propyl-2,2,2-trifluoroacetophenone

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:155628-02-7 SDS

155628-02-7Downstream Products

155628-02-7Relevant articles and documents

Catalytic asymmetric hydrogenation of α-CF3- or β-CF3-Substituted acrylic acids using Rhodium(I) complexes with a combination of chiral and achiral ligands

Dong, Kaiwu,Li, Yang,Wang, Zheng,Ding, Kuiling

supporting information, p. 14191 - 14195 (2014/01/06)

Only the mixture works! Acrylic acid derivatives with CF3 substituents in α or β position were efficiently hydrogenated in the presence of a RhI complex with a chiral secondary phosphine oxide (SPO; see scheme) and an achiral Ph3P as ligands. The corresponding propanoic acid derivatives were obtained with generally high conversion (>99 %) and high enantioselectivity (92->99 %). Copyright

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