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39580-38-6

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39580-38-6 Usage

Chemical class

Phenyl ketones

Structure

Propenone group with a bromine-substituted phenyl ring and two methylsulfanyl substituents

Applications

Organic synthesis and pharmaceutical research

Biological activities

Anti-inflammatory, antifungal, and antitumor properties

Drug development

Valuable target due to its potential biological activities

Synthesis

Versatile building block for the synthesis of various functionalized compounds

Safety

Handle with caution, may pose health hazards

Usage

Should only be used in a controlled laboratory setting

Check Digit Verification of cas no

The CAS Registry Mumber 39580-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,8 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39580-38:
(7*3)+(6*9)+(5*5)+(4*8)+(3*0)+(2*3)+(1*8)=146
146 % 10 = 6
So 39580-38-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H11BrOS2/c1-14-11(15-2)7-10(13)8-3-5-9(12)6-4-8/h3-7H,1-2H3

39580-38-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-bromophenyl)-3,3-bis(methylsulfanyl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 1-Propene-1,3-dione,3-(p-bromophenyl)-,1-(dimethyl mercaptole) (6CI)

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:39580-38-6 SDS

39580-38-6Relevant articles and documents

Transition metal free synthesis of multifunctional thiomethylated-benzenes from aryl/heteroaryl/cyclopropyl methyl ketones

Panwar, Rahul,Althagafi, Ismail,Shally,Shaw, Ranjay,Elagamy, Amr,Shah, Chandan,Yadav, Pratik,Pratap, Ramendra

, (2020/04/28)

A base-promoted strategic synthesis of various functionalized thiomethylated-benzenes has been established from aryl/heteroaryl/cyclopropyl methyl ketone. We can directly access the thiomethylated-benzene nucleus embedded with diverse functional group by

Synthesis and anti-HCV determinant motif identification in pyranone carboxamide scaffold

Balaraju, Tuniki,Konreddy, Ananda Kumar,Parveen, Afsana,Toyama, Massaki,Ito, Wataru,Karampuri, Srinivas,Baba, Masanori,Sharon, Ashoke,Bal, Chandralata

supporting information, p. 5224 - 5227 (2015/11/09)

Hepatitis C Virus exhibits high genetic diversity. The current treatment for genotype-1 with ~80% sustained virologic responses is a combination of pegylated interferon, ribavirin and boceprevir/telaprevir/simeprevir which is associated with several side

Bronsted acid catalyzed PhSe transfer versus radical aryl transfer: Linear codimerization of styrenes and internal olefins

Wu, Ping,Wang, Liandi,Wu, Kaikai,Yu, Zhengkun

supporting information, p. 868 - 871 (2015/03/30)

Bronsted acid p-TsOH·H2O-catalyzed hydrovinylation of styrenes with internal olefins α-oxo ketene dithioacetals was efficiently achieved in the presence of N-phenylselenophthalimide (N-PSP), regioselectively affording Markovnikov phenylselenati

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