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5-(4-methoxyphenyl)-1,3-oxazole-2(3H)-thione is a chemical compound with the molecular formula C10H9NO2S. It is a derivative of oxazole, a heterocyclic compound containing oxygen and nitrogen atoms. The structure of 5-(4-methoxyphenyl)-1,3-oxazole-2(3H)-thione features a 1,3-oxazole ring fused with a thiol group at the 2-position and a 4-methoxyphenyl group at the 5-position. 5-(4-methoxyphenyl)-1,3-oxazole-2(3H)-thione is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as in materials science. Its properties, such as reactivity and stability, make it a valuable intermediate in the development of various chemical products.

35801-73-1

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35801-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35801-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,0 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35801-73:
(7*3)+(6*5)+(5*8)+(4*0)+(3*1)+(2*7)+(1*3)=111
111 % 10 = 1
So 35801-73-1 is a valid CAS Registry Number.

35801-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-methoxyphenyl)-3H-1,3-oxazole-2-thione

1.2 Other means of identification

Product number -
Other names 5-(4-methoxyphenyl)-1,3-oxazole-2(3H)-thione

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

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More Details:35801-73-1 SDS

35801-73-1Downstream Products

35801-73-1Relevant academic research and scientific papers

A convenient synthesis of 2-mercapto-oxazoles via β-ketoazide and its application to a key intermediate of PI3Kγ inhibitors

Oka, Yusuke,Yabuuchi, Tetsuya,Sekiguchi, Yoshinori

, p. 1881 - 1887 (2013/10/22)

A convenient synthesis of 2-mercapto-oxazoles via the reaction of β-ketoazide with triphenylphosphine (TPP) and carbon disulfide and its application to the synthesis of a key intermediate of phosphoinositide 3-kinase γ (PI3Kγ) inhibitors are described. The Japan Institute of Heterocyclic Chemistry.

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