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2(3H)-Oxazolethione, 4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17371-97-0

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17371-97-0 Usage

Chemical Family

2(3H)-Oxazolethione, 4-phenylbelongs to the oxazolethione family.

Structure

It is a thione derivative of oxazole, containing a phenyl group at the 4th position.

Usage

It is often used in organic synthesis and pharmaceutical research as a building block or intermediate.

Applications

It has potential applications in the production of various drugs and agrochemicals.

Biological Activities

2(3H)-Oxazolethione, 4-phenylmay possess biological activities.

Pharmacological Properties

It may exhibit various pharmacological properties, making it a subject of interest in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 17371-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,7 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17371-97:
(7*1)+(6*7)+(5*3)+(4*7)+(3*1)+(2*9)+(1*7)=120
120 % 10 = 0
So 17371-97-0 is a valid CAS Registry Number.

17371-97-0SDS

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 4-phenyl-3H-1,3-oxazole-2-thione

1.2 Other means of identification

Product number -
Other names 4-phenyl-3H-oxazole-2-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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17371-97-0 SDS

17371-97-0Relevant academic research and scientific papers

Pyridinium ylides in the synthesis of 2,3-dihydrofurans

Chuang, Che-Ping,Tsai, An-I.

, p. 675 - 679 (2006)

A new method for the synthesis of 2,3-dihydrofurans from readily available starting enones and pyridinium salts has been developed. This protocol can provide a novel and effective methodology for the preparation of 2,3-dihydrofurans in a stereoselective f

Tetrazolinone compound and application for same

-

Paragraph 0738; 0739; 0740; 0741, (2016/10/08)

Provided is a tetrazolinone compound given by formula (1) (wherein E represents a 5-membered aromatic hetero group, such as the pyrazolyl group, the thiazolyl group, or the imidazolyl group; R4 and R5 represent hydrogen atoms or the like; R6 represents a C1-12 alkyl group; R7, R8, and R9 represent hydrogen atoms or the like; R10 represents a C1-3 alkyl group, or a C1-3 haloalkyl group; Y represents an oxygen atom or the like; and Q represents an oxygen atom or the like), and having exceptional efficacy in controlling harmful organisms.

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