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3-(phenyl(phenylthio)methyl)pentane-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51679-37-9

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51679-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51679-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,7 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51679-37:
(7*5)+(6*1)+(5*6)+(4*7)+(3*9)+(2*3)+(1*7)=139
139 % 10 = 9
So 51679-37-9 is a valid CAS Registry Number.

51679-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(phenyl(phenylthio)methyl)pentane-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-(α-phenylsulfanyl-benzyl)-pentane-2,4-dione

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:51679-37-9 SDS

51679-37-9Downstream Products

51679-37-9Relevant academic research and scientific papers

Synthesis of Unsymmetrical Sulfides and Their Oxidation to Sulfones to Discover Potent Antileishmanial Agents

Dar, Ajaz A.,Enjamuri, Nagasuresh,Shadab,Ali, Nahid,Khan, Abu T.

supporting information, p. 671 - 681 (2015/11/17)

Unsymmetrical sulfides were first synthesized using combinations of a 1,3-dicarbonyl, an aromatic aldehyde and a thiol in the presence of 10 mol % ethanolic piperidine. These sulfides derivatives were subsequently converted into corresponding sulfones via

C-H bond oxidation initiated pummerer- And knoevenagel-Type reactions of benzyl sulfide and 1,3-dicarbonyl compounds

Li, Zhiping,Li, Haijun,Guo, Xingwei,Cao, Lin,Yu, Rong,Li, Huanrong,Pan, Shiguang

supporting information; experimental part, p. 803 - 805 (2009/04/06)

A novel Pummerer-type reaction was developed via o-chloranil-mediated C-H bond oxidation. The reaction provides a simple and efficient method to construct sulfide derivatives. A Knoevenagel-type reaction was also achieved via multiple C-H bonds activation under neutral reaction conditions.

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