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1,5-Pentanedione, 3-methyl-2-methylene-1,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112583-77-4

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112583-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112583-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,5,8 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 112583-77:
(8*1)+(7*1)+(6*2)+(5*5)+(4*8)+(3*3)+(2*7)+(1*7)=114
114 % 10 = 4
So 112583-77-4 is a valid CAS Registry Number.

112583-77-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dibenzoyl-3-methylbutene

1.2 Other means of identification

Product number -
Other names -

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:112583-77-4 SDS

112583-77-4Relevant academic research and scientific papers

REACTIONS OF 1,5-DIKETONES. XLIX. SYNTHESIS OF THE PHENYL ANALOG OF THE ALKALOID ONYCHINE

Pavel', G. V.,Mel'nik, I. A.,Tilichenko, M. N.

, p. 758 - 760 (2007/10/02)

1-Methyl-3-phenyl-4-azafluorene was obtained by intramolecular cyclization of 2,4-dibenzoyl-3-methylbutene by the action of sulfuric acid followed by closure of the pyridine ring in the obtained 2-(3-oxo-1-methyl-3-phenylpropyl)-1-indanone by the action o

An Efficient and Convenient Method for the Preparation of α-Methylenated Ketones from Silyl Enol Ethers

Hayashi, Masaji,Mukaiyama, Teruaki

, p. 1283 - 1286 (2007/10/02)

In the presence of a catalytic amount of stannous halide, silyl enol ethers react with bromomethyl methyl ether to give the corresponding α-bromoethyl ketones, which are smoothly converted to α-methylenated ketones on the successive addition of tertiary amine by one-pot procedure.This method is successfully applied to a synthesis of sarkomycin intermediate.

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