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60283-15-0

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60283-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60283-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,8 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60283-15:
(7*6)+(6*0)+(5*2)+(4*8)+(3*3)+(2*1)+(1*5)=100
100 % 10 = 0
So 60283-15-0 is a valid CAS Registry Number.

60283-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-acetylphenyl)-2,2,2-trifluoroethanone

1.2 Other means of identification

Product number -
Other names 1-(3-ACETYLPHENYL)-2,2,2-TRIFLUORO-ETHANONE

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:60283-15-0 SDS

60283-15-0Downstream Products

60283-15-0Relevant articles and documents

Chemo- and Stereoselective Synthesis of Fluorinated Amino Alcohols through One-pot Reactions using Alcohol Dehydrogenases and Amine Transaminases

González-Martínez, Daniel,Gotor, Vicente,Gotor-Fernández, Vicente

supporting information, p. 5398 - 5410 (2020/10/06)

A series of amino alcohols have been prepared in a chemo-, diastereo- and enantioselective fashion starting from the corresponding (het)aryl diketones, avoiding tedious chemical protection and deprotection steps. Different alcohol dehydrogenases have been

Chemoselective reduction of ketones: Trifluoromethylketones versus methylketones

Sasaki, Shigeru,Yamauchi, Takayasu,Kubo, Hajime,Kanai, Masatomi,Ishii, Akihiro,Higashiyama, Kimio

, p. 1497 - 1500 (2007/10/03)

Treatment of an equimolar mixture of trifluoromethylketones (TFMKs) and methylketones (MKs) with Et2Zn resulted in selective reduction of the TFMKs in good yield. In contrast, treatment of an equimolar mixture of TFMKs and MKs with NaBH4 in the presence of CeCl3 in EtOH/H 2O (10:1) at -10°C reduced only the MKs.

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