Cas 143210-75-7,4H-3,1-Benzothiazine-6-carboxylic acid, 2-amino-5,6-dihydro-7-methyl-5-(3-nitrophenyl)-4-oxo-, ethyl ester

143210-75-7

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Basic information

Product Name: 4H-3,1-Benzothiazine-6-carboxylic acid, 2-amino-5,6-dihydro-7-methyl-5-(3-nitrophenyl)-4-oxo-, ethyl ester
Synonyms:
CAS NO:143210-75-7
Molecular Formula: C18H17N3O5S
Molecular Weight: 387.416
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: 4H-3,1-Benzothiazine-6-carboxylic acid, 2-amino-5,6-dihydro-7-methyl-5-(3-nitrophenyl)-4-oxo-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4H-3,1-Benzothiazine-6-carboxylic acid, 2-amino-5,6-dihydro-7-methyl-5-(3-nitrophenyl)-4-oxo-, ethyl ester(143210-75-7)
EPA Substance Registry System: 4H-3,1-Benzothiazine-6-carboxylic acid, 2-amino-5,6-dihydro-7-methyl-5-(3-nitrophenyl)-4-oxo-, ethyl ester(143210-75-7)

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: 143210-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143210-75-7 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 143210-75:
(8*1)+(7*4)+(6*3)+(5*2)+(4*1)+(3*0)+(2*7)+(1*5)=87
87 % 10 = 7
So 143210-75-7 is a valid CAS Registry Number.

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143210-75-7Relevant 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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