Cas 4695-22-1,5-methyl-3-phenyl-2-(N-phenylimino)-1,3-thiazolidin-4-one

4695-22-1

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Basic information

Product Name: 5-methyl-3-phenyl-2-(N-phenylimino)-1,3-thiazolidin-4-one
Synonyms: 5-methyl-3-phenyl-2-(N-phenylimino)-1,3-thiazolidin-4-one
CAS NO:4695-22-1
Molecular Formula:
Molecular Weight: 282.366
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-methyl-3-phenyl-2-(N-phenylimino)-1,3-thiazolidin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 5-methyl-3-phenyl-2-(N-phenylimino)-1,3-thiazolidin-4-one(4695-22-1)
EPA Substance Registry System: 5-methyl-3-phenyl-2-(N-phenylimino)-1,3-thiazolidin-4-one(4695-22-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 4695-22-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 4695-22-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,9 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4695-22:
(6*4)+(5*6)+(4*9)+(3*5)+(2*2)+(1*2)=111
111 % 10 = 1
So 4695-22-1 is a valid CAS Registry Number.

4695-22-1Upstream product

4695-22-1Downstream Products

1012-88-0 5-methyl-3-phenyl-thiazolidine-2,4-dione

4695-22-1Relevant academic research and scientific papers

Efficient synthetic procedure to new 2-imino-1,3-thiazolines and thiazolidin-4-ones promoted by acetonitrile electrogenerated base

Haouas, Beya,Sbei, Najwa,Ayari, Hana,Benkhoud, M. Lamine,Batanero, Belen

, p. 11776 - 11781 (2018)

A novel and convenient strategy is described for the regioselective conversion of N,N′-disubstituted thioureas and 1,2-dielectrophiles into the highly biologically valuable 2-imino-thiazoline and 2-imino thiazolidine-4-one derivatives. The synthesis proce

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