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2-Amino-5-[(p-methoxyphenyl)thiomethyl]-2-oxazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50510-13-9

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50510-13-9 Usage

Properties

Contains an oxazoline ring, amino group, thiomethyl substituent, and p-methoxyphenyl group

Usage

Organic synthesis, medicinal chemistry, pharmaceutical development

Potential applications

Treatment of diseases, building block for complex organic compounds

Additional uses

Reagent, catalyst in organic reactions

Check Digit Verification of cas no

The CAS Registry Mumber 50510-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,1 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50510-13:
(7*5)+(6*0)+(5*5)+(4*1)+(3*0)+(2*1)+(1*3)=69
69 % 10 = 9
So 50510-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O2S/c1-14-8-2-4-10(5-3-8)16-7-9-6-13-11(12)15-9/h2-5,9H,6-7H2,1H3,(H2,12,13)

50510-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(4-methoxyphenyl)sulfanylmethyl]-4,5-dihydro-1,3-oxazol-2-amine

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:50510-13-9 SDS

50510-13-9Downstream Products

50510-13-9Relevant academic research and scientific papers

Sulfenocyclization of Unsaturated Ureas and Thioureas

El-Samii, Z. K. Abd

, p. 609 - 614 (2007/10/02)

A general method for the formation of cyclic sulfenylated 2-oxazoline, 2-thiazolines, 5,6-dihydro-4H-1,3-oxazines, and 5,6-dihydro-4H-1,3-thiazines is described.The procedure employs arylsulfenyl chloride and ethyldiisopropylamine to generate an episulfon

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