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139373-54-9

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139373-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139373-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,3,7 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 139373-54:
(8*1)+(7*3)+(6*9)+(5*3)+(4*7)+(3*3)+(2*5)+(1*4)=149
149 % 10 = 9
So 139373-54-9 is a valid CAS Registry Number.

139373-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-5-phenyl-3-(2-phenylethyl)pentan-2-one

1.2 Other means of identification

Product number -
Other names 2-Pentanone,3-methyl-5-phenyl-3-(2-phenylethyl)

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:139373-54-9 SDS

139373-54-9Downstream Products

139373-54-9Relevant articles and documents

Non-dehydrative pinacol rearrangement using a Lewis acid-trialkyl orthoester combined system

Kita, Yasuyuki,Yoshida, Yutaka,Mihara, Sachiko,Furukawa, Akihiro,Higuchi, Kazuhiro,Fang, Dai-Fei,Fujioka, Hiromichi

, p. 14689 - 14704 (2007/10/03)

An efficient pinacol rearrangement mediated by trialkyl orthoformate has been developed. The reactions of various types of diols with a catalytic amount of a Lewis acid in the presence of an orthoester afforded the rearranged product in good yields via a cyclic orthoester intermediate. This combined system is applicable not only to cyclic and acyclic tri- and tetra- substituted diols but also to the diols having acid-sensitive acetals.

The Catalytic Pinacol Rearrangement of 1,2-Diols Using an Antimony(V)Salt

Harada, Tsunehiro,Mukaiyama, Teruaki

, p. 81 - 84 (2007/10/02)

In the presence of a catalytic amount of antimony(V)chloride or antimony(V)salt generated from antimony(V)chloride and silver hexafluoroantimonate, the pinacol rearrangement of several 1,2-diols or their trimethylsilyl ethers proceeds smoothly to give the corresponding ketones in good yields.

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