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1520-46-3

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1520-46-3 Usage

General Description

1,3-DIPHENYL-2-METHYLPROPANE is a chemical compound with the molecular formula C19H20. It is a colorless liquid with a molecular weight of 248.36 g/mol. 1,3-DIPHENYL-2-METHYLPROPANE is primarily used in organic synthesis as a building block for the production of various pharmaceuticals, agrochemicals, and other fine chemicals. Its structure consists of a central carbon atom with two phenyl groups and one methyl group attached to it. The compound has several isomers and can be synthesized through various reactions, including Friedel-Crafts alkylation and McMurry coupling. 1,3-DIPHENYL-2-METHYLPROPANE is also known by other names, including 1,3-diphenyl-2-methylpropane and isopropyldiphenylmethane.

Check Digit Verification of cas no

The CAS Registry Mumber 1520-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1520-46:
(6*1)+(5*5)+(4*2)+(3*0)+(2*4)+(1*6)=53
53 % 10 = 3
So 1520-46-3 is a valid CAS Registry Number.

1520-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methyl-3-phenylpropyl)benzene

1.2 Other means of identification

Product number -
Other names 1,1-Dibenzyl-aethan

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:1520-46-3 SDS

1520-46-3Downstream Products

1520-46-3Relevant articles and documents

Iron-Catalyzed Remote Arylation of Aliphatic C-H Bond via 1,5-Hydrogen Shift

Zhou, Bingwei,Sato, Hiroki,Ilies, Laurean,Nakamura, Eiichi

, p. 8 - 11 (2018/01/17)

Catalytic amounts of an iron(III) salt and a N-heterocyclic carbene ligand catalyze the arylation of 2-iodoalkylarenes with diphenylzinc selectively at the C-H bond of the alkyl side chain. Several lines of evidence suggest that the iron catalyst reacts with the aryl iodide moiety of the substrate to generate an aryliron intermediate that behaves in a radical manner and cleaves the aliphatic C-H bond through 1,5-hydrogen transfer; the resulting alkyliron intermediate undergoes reductive elimination to give the arylated product.

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