Cas 138990-70-2,4-Thiazoleacetamide, 2-(1-acetyl-2-oxopropylidene)-2,3-dihydro-N-(4-methylphenyl)-3-phenyl-

138990-70-2

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Basic information

Product Name: 4-Thiazoleacetamide, 2-(1-acetyl-2-oxopropylidene)-2,3-dihydro-N-(4-methylphenyl)-3-phenyl-
Synonyms:
CAS NO:138990-70-2
Molecular Formula: C23H22N2O3S
Molecular Weight: 406.505
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: 4-Thiazoleacetamide, 2-(1-acetyl-2-oxopropylidene)-2,3-dihydro-N-(4-methylphenyl)-3-phenyl-(CAS DataBase Reference)
NIST Chemistry Reference: 4-Thiazoleacetamide, 2-(1-acetyl-2-oxopropylidene)-2,3-dihydro-N-(4-methylphenyl)-3-phenyl-(138990-70-2)
EPA Substance Registry System: 4-Thiazoleacetamide, 2-(1-acetyl-2-oxopropylidene)-2,3-dihydro-N-(4-methylphenyl)-3-phenyl-(138990-70-2)

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: 138990-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138990-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,9 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138990-70:
(8*1)+(7*3)+(6*8)+(5*9)+(4*9)+(3*0)+(2*7)+(1*0)=172
172 % 10 = 2
So 138990-70-2 is a valid CAS Registry Number.

138990-70-2Upstream product

138990-70-2Downstream Products

138990-70-2Relevant academic research and scientific papers

γ-BROMOACETOACETANILIDES IN HETEROCYCLIC SYNTHESIS: A CONVENIENT SYNTHESIS OF POLYFUNCTIONALLY SUBSTITUTED 2,3-DIHYDROTHIAZOLE, PYRIDIN-2-ONE, 1,2,3-TRIAZINE, OXAZOLOPYRIDINE AND PYRAZOLOPYRIDINE DERIVATIVES

Mohareb, Rafat M.,Abdel-Sayed, Nadia I.,Sherif, Sherif M.

, p. 119 - 130 (2007/10/02)

The active methylene reagents 1a-d reacted with phenyl isothiocyanate in basic DMF at room temperature to yield the non-isolable 1:1 adducts 2a-d.In situ cyclization of the latter with γ-bromoacetoanilides afforded the 2,3-dihydrothiazoles 3a-h.The reacti

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