Cas 125041-02-3,Pyrido[2,3-d]pyridazine-8-carboxylic acid, 2,4-diamino-6-(4-chlorophenyl)-3-cyano-5,6-dihydro-5-imino-, ethyl ester

125041-02-3

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Basic information

Product Name: Pyrido[2,3-d]pyridazine-8-carboxylic acid, 2,4-diamino-6-(4-chlorophenyl)-3-cyano-5,6-dihydro-5-imino-, ethyl ester
Synonyms:
CAS NO:125041-02-3
Molecular Formula: C17H14ClN7O2
Molecular Weight: 383.797
EINECS: N/A
Product Categories: N/A
Mol File: 125041-02-3.mol

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: Pyrido[2,3-d]pyridazine-8-carboxylic acid, 2,4-diamino-6-(4-chlorophenyl)-3-cyano-5,6-dihydro-5-imino-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Pyrido[2,3-d]pyridazine-8-carboxylic acid, 2,4-diamino-6-(4-chlorophenyl)-3-cyano-5,6-dihydro-5-imino-, ethyl ester(125041-02-3)
EPA Substance Registry System: Pyrido[2,3-d]pyridazine-8-carboxylic acid, 2,4-diamino-6-(4-chlorophenyl)-3-cyano-5,6-dihydro-5-imino-, ethyl ester(125041-02-3)

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: 125041-02-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 125041-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,0,4 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125041-02:
(8*1)+(7*2)+(6*5)+(5*0)+(4*4)+(3*1)+(2*0)+(1*2)=73
73 % 10 = 3
So 125041-02-3 is a valid CAS Registry Number.

125041-02-3Upstream product

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125041-02-3Relevant academic research and scientific papers

Studies on Alkyl Heterocyclic Aromatic Compounds: New Routes for the Synthesis of Polyazanaphthalenes

Elnagdi, Mohamed Hilmy,Aal, Fatma Abdel Maksoud Abdel,Hafez, Ebtisam Abdel Aziz,Yassin, Youssef Mahfouz

, p. 683 - 689 (2007/10/02)

Several new polyfunctionally substituted polyazanaphthalene derivatives could be synthesized via condensing readily obtainable polyfunctional nitriles with substituted akyl heteroaromatic derivatives and reacting the latter derivatives with electrophilic

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