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2-Ethyl-1,2-diphenylbutan-1-ol is an organic compound with the molecular formula C20H24O. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is classified as a secondary alcohol due to the presence of a hydroxyl group (-OH) attached to a carbon atom bonded to two other carbon atoms. 2-ethyl-1,2-diphenylbutan-1-ol is characterized by a butane chain with an ethyl group at the 2nd position, and two phenyl rings attached to the 1st and 2nd carbon atoms. It is a colorless liquid with a distinct aromatic odor and is insoluble in water but soluble in organic solvents. 2-Ethyl-1,2-diphenylbutan-1-ol has potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals, as well as in the field of materials science.

5351-08-6

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5351-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5351-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5351-08:
(6*5)+(5*3)+(4*5)+(3*1)+(2*0)+(1*8)=76
76 % 10 = 6
So 5351-08-6 is a valid CAS Registry Number.

5351-08-6SDS

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-ethyl-1,2-diphenylbutan-1-ol

1.2 Other means of identification

Product number -
Other names 2-Aethyl-1,2-diphenyl-butan-1-ol

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:5351-08-6 SDS

5351-08-6Relevant academic research and scientific papers

Enantioselective hydrogenation and transfer hydrogenation of bulky ketones catalysed by a ruthenium complex of a chiral tridentate ligand

Diaz-Valenzuela, M. Belen,Phillips, Scott D.,France, Marcia B.,Gunn, Mary E.,Clarke, Matthew L.

supporting information; experimental part, p. 1227 - 1232 (2009/08/10)

A study on the enantioselective hydrogenation of tertiary alkyl ketones catalysed by a novel class of tridentate-Ru complex is reported. In contrast to the extensively studied [RuCl2(diphos)(di-primary amine)] complexes, this new class of hydro

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