Cas 143210-77-9,6-Quinazolinecarboxylic acid, 2,3,4,4a,5,6-hexahydro-5-(4-methoxyphenyl)-7-methyl-2,4-dioxo-, ethyl ester

143210-77-9

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Basic information

Product Name: 6-Quinazolinecarboxylic acid, 2,3,4,4a,5,6-hexahydro-5-(4-methoxyphenyl)-7-methyl-2,4-dioxo-, ethyl ester
Synonyms:
CAS NO:143210-77-9
Molecular Formula: C19H20N2O5
Molecular Weight: 356.378
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: 6-Quinazolinecarboxylic acid, 2,3,4,4a,5,6-hexahydro-5-(4-methoxyphenyl)-7-methyl-2,4-dioxo-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-Quinazolinecarboxylic acid, 2,3,4,4a,5,6-hexahydro-5-(4-methoxyphenyl)-7-methyl-2,4-dioxo-, ethyl ester(143210-77-9)
EPA Substance Registry System: 6-Quinazolinecarboxylic acid, 2,3,4,4a,5,6-hexahydro-5-(4-methoxyphenyl)-7-methyl-2,4-dioxo-, ethyl ester(143210-77-9)

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: 143210-77-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143210-77-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,1 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143210-77:
(8*1)+(7*4)+(6*3)+(5*2)+(4*1)+(3*0)+(2*7)+(1*7)=89
89 % 10 = 9
So 143210-77-9 is a valid CAS Registry Number.

143210-77-9Upstream product

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143210-77-9Relevant academic research and scientific papers

Synthesis of condensed heterocycles from 3-aryl-2,4-dicarbethoxy-5-methylcyclohexanones and their testing for antimicrobial activity

Metwally,El-Hossini,El-Ablak,Khalil

, p. 336 - 339 (2007/10/02)

Condensation of the title compounds (1) with hydroxylamine hydrochloride, hydrazines and/or aromatic amines resulted in the formation of the benzisoxazoles 2, oximes 3, indazolines 4 and β-keto anilides 6. The oxime derivatives and anilides underwent cycl

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