Cas 1217509-43-7,5-(2-amino-4-(4-fluorophenyl)thiazol-5-yl)-6-hydroxy-1,3-dimethylpyrimidine-2,4(1H,3H)-dione

1217509-43-7

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Basic information

Product Name: 5-(2-amino-4-(4-fluorophenyl)thiazol-5-yl)-6-hydroxy-1,3-dimethylpyrimidine-2,4(1H,3H)-dione
Synonyms:
CAS NO:1217509-43-7
Molecular Formula:
Molecular Weight: 348.358
EINECS: N/A
Product Categories: N/A
Mol File: 1217509-43-7.mol
Article Data: 1

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-(2-amino-4-(4-fluorophenyl)thiazol-5-yl)-6-hydroxy-1,3-dimethylpyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5-(2-amino-4-(4-fluorophenyl)thiazol-5-yl)-6-hydroxy-1,3-dimethylpyrimidine-2,4(1H,3H)-dione(1217509-43-7)
EPA Substance Registry System: 5-(2-amino-4-(4-fluorophenyl)thiazol-5-yl)-6-hydroxy-1,3-dimethylpyrimidine-2,4(1H,3H)-dione(1217509-43-7)

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: 1217509-43-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1217509-43-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,5,0 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1217509-43:
(9*1)+(8*2)+(7*1)+(6*7)+(5*5)+(4*0)+(3*9)+(2*4)+(1*3)=137
137 % 10 = 7
So 1217509-43-7 is a valid CAS Registry Number.

1217509-43-7Upstream product

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1217509-43-7Relevant articles and documents

Investigations on 5-(2-aryl-2-oxo-ethylidene)-1,3-dimethylbarbituric and thiobarbituric acids: Reactions with thioureas and thioacetamide

Kolos,Zamigaylo,Musatov

experimental part, p. 970 - 975 (2010/03/26)

Derivatives of 2-amino- and 2-methylthiazole have been synthesized by the reaction of 5-(2-aryl-2-oxoethylidene)-1,3-dimethylbarbituric and thiobarbituric acids with thioureas and thioacetamide, and also by a one-pot synthesis involving thiourea (or thioa

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