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Acetamide, 2-(phenylsulfinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

49639-34-1

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49639-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49639-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,3 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 49639-34:
(7*4)+(6*9)+(5*6)+(4*3)+(3*9)+(2*3)+(1*4)=161
161 % 10 = 1
So 49639-34-1 is a valid CAS Registry Number.

49639-34-1SDS

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-(benzenesulfinyl)acetamide

1.2 Other means of identification

Product number -
Other names Phenylsulfinyl-acetamid

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:49639-34-1 SDS

49639-34-1Downstream Products

49639-34-1Relevant academic research and scientific papers

One-Pot Sequential Multistep Transformation of α,β-Unsaturated Trifluoromethyl Ketones: Facile Synthesis of Trifluoromethylated 2-Pyridones

Lv, Ning,Tian, Yi-Qiang,Zhang, Fa-Guang,Ma, Jun-An

supporting information, p. 605 - 609 (2019/03/07)

A one-pot transformation of α,β-unsaturated trifluoromethyl ketones with 2-(phenylsulfinyl)acetamide to give trifluoromethylated 2-pyridones is realized. The reaction proceeds under mild conditions and involves multiple steps in an expeditious and controlled sequence to provide efficient access to a broad range of trifluoromethylated 2-pyridones in moderate to high yields. Moreover, further synthetic manipulations permit the routine synthesis of a diverse array of trifluoromethylated pyridines with good efficiency.

2-pyridone synthesis using 2-(phenylsulfinyl)acetamide

Fujii, Masaya,Nishimura, Takuya,Koshiba, Takahiro,Yokoshima, Satoshi,Fukuyama, Tohru

supporting information, p. 232 - 234 (2013/04/10)

2-Pyridones were prepared by means of an efficient protocol including the 1,4-addition of 2-(phenylsulfinyl)acetamide to α,β-unsaturated ketones followed by cyclization and sulfoxide elimination.

EFFECT OF MOLECULAR STRUCTURE ON OPTICAL PROPERTIES OF SULFOXIDE SYSTEMS. PHENYL- AND m-BROMOPHENYLSULFINYLACETIC ACIDS AND SOME OF THEIR DERIVATIVES. PART I

Janczewski, Marian,Najda, Teresa,Jablonska-Pikus, Teresa

, p. 1297 - 1312 (2007/10/02)

The synthesis of phenylsulfinyl- and sulfonyl-acetic acids and their m-bromo derivatives is described.The racemic sulfoxides were resolved into enantiomers.The absolute configurations of enantiomers were elucitated.The optical rotatory dispersion of laevorotatory enantiomers, their amides, p-nitrobenzyl and p-bromophenacyl esters was determined.

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