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138249-74-8

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138249-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138249-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,2,4 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138249-74:
(8*1)+(7*3)+(6*8)+(5*2)+(4*4)+(3*9)+(2*7)+(1*4)=148
148 % 10 = 8
So 138249-74-8 is a valid CAS Registry Number.

138249-74-8SDS

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 2-(2,2,2-trifluoro-1-hydroxyethyl)cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-(2,2,2-trifluoro-1-hydroxyethyl)cyclohexanone

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:138249-74-8 SDS

138249-74-8Downstream Products

138249-74-8Relevant articles and documents

Organocatalytic asymmetric direct aldol reactions of trifluoroacetaldehyde ethyl hemiacetal with aromatic methyl ketones

Funabiki, Kazumasa,Itoh, Yuya,Kubota, Yasuhiro,Matsui, Masaki

experimental part, p. 3545 - 3550 (2011/06/22)

The organocatalytic asymmetric direct aldol reaction of trifluoroacetaldehyde ethyl hemiacetal with aromatic methyl ketones in the presence of a catalytic amount of (S)-5-(pyrrolidin-2-yl)-1H-tetrazole in dichloroethane at 40 °C proceeds smoothly to produ

Facile Synthesis of α-Trifluoromethylated Alcohols from Trifluoroacetaldehyde Ethyl Hemiacetal

Kubota, Toshio,Iijima, Masahiro,Tanaka, Tatsuo

, p. 1351 - 1354 (2007/10/02)

Trifluoroacetaldehyde ethyl hemiacetal reacted with nucleophilic organosilanes such as cyanotrimethylsilane, allyltrimethylsilane, or enol trimethylsilyl ethers in the presence of Lewis acid to afford a series of α-trifluoromethylated alcohols in high yield. Key Words: trifluoroacetaldehyde ethyl hemiacetal; Lewis acid; trimethylsilylated nucleophiles; carbon-carbon bond formation; α-trifluoromethylated alcohol.

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