Cas 862534-98-3,3-benzylideneamino-8,9-diphenylpyridazino[4',3':4,5]thieno[3,2-d]-1,2,3-triazin-4(3H)-one

862534-98-3

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Basic information

Product Name: 3-benzylideneamino-8,9-diphenylpyridazino[4',3':4,5]thieno[3,2-d]-1,2,3-triazin-4(3H)-one
Synonyms: 3-benzylideneamino-8,9-diphenylpyridazino[4',3':4,5]thieno[3,2-d]-1,2,3-triazin-4(3H)-one
CAS NO:862534-98-3
Molecular Formula:
Molecular Weight: 460.519
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: 3-benzylideneamino-8,9-diphenylpyridazino[4',3':4,5]thieno[3,2-d]-1,2,3-triazin-4(3H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-benzylideneamino-8,9-diphenylpyridazino[4',3':4,5]thieno[3,2-d]-1,2,3-triazin-4(3H)-one(862534-98-3)
EPA Substance Registry System: 3-benzylideneamino-8,9-diphenylpyridazino[4',3':4,5]thieno[3,2-d]-1,2,3-triazin-4(3H)-one(862534-98-3)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 862534-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 862534-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,5,3 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 862534-98:
(8*8)+(7*6)+(6*2)+(5*5)+(4*3)+(3*4)+(2*9)+(1*8)=193
193 % 10 = 3
So 862534-98-3 is a valid CAS Registry Number.

862534-98-3Upstream product

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862534-98-3Relevant academic research and scientific papers

Pyridazine derivatives and related compounds, Part 12: Synthesis of some pyridazino [4′,3′:4,5]thieno[3,2-d]-1,2,3-triazines

Deeb, Ali,Kotb, Mahmoud,El-Abbasy, Mohamed

, p. 591 - 599 (2007/10/03)

The syntheses of pyridazino[4′,3′:4, 5]thieno[3, 2-d]-1,2,3-triazinones 2, 3, 6, derivatives of the ring system thieno[2,3-c]pyridazine, have been accomplished by a diazotization reaction. Reaction of triazine 3 with phosphorous oxychloride led to 4-chlor

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