Cas 503056-30-2,Acetamide, 2-[2-[[[(4-hydroxyphenyl)methylene]amino]thioxomethyl]hydrazino]-N-(2- methyl-4-oxo-3(4H)-quinazolinyl)-

503056-30-2

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Basic information

Product Name: Acetamide, 2-[2-[[[(4-hydroxyphenyl)methylene]amino]thioxomethyl]hydrazino]-N-(2- methyl-4-oxo-3(4H)-quinazolinyl)-
Synonyms:
CAS NO:503056-30-2
Molecular Formula: C19H18N6O3S
Molecular Weight: 410.456
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: Acetamide, 2-[2-[[[(4-hydroxyphenyl)methylene]amino]thioxomethyl]hydrazino]-N-(2- methyl-4-oxo-3(4H)-quinazolinyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Acetamide, 2-[2-[[[(4-hydroxyphenyl)methylene]amino]thioxomethyl]hydrazino]-N-(2- methyl-4-oxo-3(4H)-quinazolinyl)-(503056-30-2)
EPA Substance Registry System: Acetamide, 2-[2-[[[(4-hydroxyphenyl)methylene]amino]thioxomethyl]hydrazino]-N-(2- methyl-4-oxo-3(4H)-quinazolinyl)-(503056-30-2)

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: 503056-30-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 503056-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,0,5 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 503056-30:
(8*5)+(7*0)+(6*3)+(5*0)+(4*5)+(3*6)+(2*3)+(1*0)=102
102 % 10 = 2
So 503056-30-2 is a valid CAS Registry Number.

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503056-30-2Downstream Products

503056-30-2Relevant academic research and scientific papers

Synthesis and blood pressure lowering activity of some newer quinazolinones

Tyagi, Mirdula,Srivastava,Chandra, Ramesh,Kumar, Ashok

, p. 2367 - 2370 (2007/10/03)

Some new 3-[3′-(aminoacetylthiosemicarbazido)-4′-oxo-2′- (substituted-aryl)-1′-thiazolidinyl]-2-methylmonosubstituted- quinazolin-4(3H)-ones 5a-j have been synthesized by 1,5 cyclocondensation of thioglycolic acid with 3-(aminoacetylthiosemicarbazidosubst

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