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2-(1,3-benzoxazol-2-ylsulfanyl)-N-(2,5-dimethoxyphenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5356-55-8

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5356-55-8 Usage

Molecular weight

355.4

Structural features

Contains a benzoxazol ring, a sulfanyl group, an acetamide group, and two methoxyphenyl groups

Potential pharmaceutical applications

May interact with biological targets due to its structural features

Research and testing needs

Further research and testing are required to determine its specific properties, potential uses, and pharmacological effects.

Check Digit Verification of cas no

The CAS Registry Mumber 5356-55-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5356-55:
(6*5)+(5*3)+(4*5)+(3*6)+(2*5)+(1*5)=98
98 % 10 = 8
So 5356-55-8 is a valid CAS Registry Number.

5356-55-8SDS

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-(1,3-benzoxazol-2-ylsulfanyl)-N-(2,5-dimethoxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names acetamide,2-(2-benzoxazolylthio)-n-(2,5-dimethoxyphenyl)

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:5356-55-8 SDS

5356-55-8Downstream Products

5356-55-8Relevant academic research and scientific papers

Biomimetic oxidation of 3β-hydroxy-olean-12-ene and its acetoxy derivative with monooxygen donors catalyzed by 5,10,15,20-tetraarylporphyrinatoiron(III) chlorides in dichloromethane

Chauhan,Mohapatra,Mamta,Parkash,Azam

, p. 183 - 189 (2007/10/03)

The oxidation of 3β-hydroxy-olean-12-ene with monooxygen donors catalyzed by 5,10,15,20-tetraarylporphyrinatoiron(III) chlorides in dichloromethane gives 3β,11α-dihydroxy-olean-12-ene, 3-oxo-olean-12-ene, 3,11-dioxo-olean-12-ene and 3β-hydroxy-olean-9(11),12-diene whereas the oxidation of 3β-acetoxy-olean-12-ene under similar conditions gives 11(-hydroxy-3β-acetoxy-olean-12-ene, 11-oxo-3β-acetoxy-olean-12-ene and 3β-acetoxy-olean-9(11),12-diene in moderate yields.

Triterpenes of Diospyros peregrina Gurke: Partial Synthesis of Olean-9(11),12-dien-3-one and Ursan-9(11),12-dien-3-one (Marsformosanone)

Bhaumik, Tapanjyoti,Dey, A. K.,Das, P. C.,Mukhopadhyay, A. K.,Chatterjee, A.

, p. 664 - 668 (2007/10/02)

Petrol extract of the fruits of Diospyros peregrina (Ebenaceae) has afforded a pentacyclic triterpene ketone with a homoannular diene system, besides betulin and lupeol.In order to establish the structure of the ketone, partial synthesis of both olean- and ursan-9(11),12-dien-3-ones have been achieved.The structure of the pentacyclic triterpene ketone has been established as marsformosanone (II) from spectral data, chemical reactions and synthesis.The occurrence of marsformosanone in Marsdenia formosana Masamune has been recently reported .

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