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

83507-17-9

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83507-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83507-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,0 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83507-17:
(7*8)+(6*3)+(5*5)+(4*0)+(3*7)+(2*1)+(1*7)=129
129 % 10 = 9
So 83507-17-9 is a valid CAS Registry Number.

83507-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-2-phenylimino-1,3-thiazolidin-5-one

1.2 Other means of identification

Product number -
Other names 3-phenyl-2-phenyliminothiazolidin-5-one

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:83507-17-9 SDS

83507-17-9Relevant academic research and scientific papers

Synthesis of some new thiazolidin-5-one derivatives of pharmaceutical interest

Metwally,Keshk,Fekry,Etman

, p. 2067 - 2079 (2007/10/03)

Condensation of thiazolidin-5-one derivative 1 with different aromatic aldehydes gave the corresponding arylidenes 2a-e. Compound 2e was reacted with urea and thiourea to give the corresponding thiazolo[5,4-d]pyrimidine derivatives 3a,b, respectively. Treatment of compound 1 with phenyl isothiocyanate in basic DMF gave the nonisolable potassium salt of the adduct 4, which underwent heterocyclization upon treatment with chloroacetyl chloride and phenacyl bromide to give the corresponding [2,4′] bisthiazolidinylidenes 5 and 8. Moreover, the reactions of compound 1 with a variety of reagents, e.g., ninhydrin and isatin, were investigated. The structures of these compounds were established by analytical and spectral data.

A FACILE SYNTHESIS OF THIAZOLIDIN-5-ONES AND THEIR STRUCTURAL ASSINGMENT

Okawara, Tadashi,Nakayama, Kentaro,Furukawa, Mitsuru

, p. 1571 - 1574 (2007/10/02)

The reaction of 1,3-disubstituted thioureas (I) with α-halacyl halides (II) was found to afford thiazolidin-5-ones (IV) in 5percent sodium hydroxide-dichloromethane in the yields of 34-89percent.The structures of IV were discussed in details.

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