Cas 874461-75-3,2,4(1H,3H)-Pyrimidinedione, 5-(6H-cyclohepta[b]naphthalen-6-yl)-1,3-dimethyl-6-(phenylamino)-

874461-75-3

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Basic information

Product Name: 2,4(1H,3H)-Pyrimidinedione, 5-(6H-cyclohepta[b]naphthalen-6-yl)-1,3-dimethyl-6-(phenylamino)-
Synonyms:
CAS NO:874461-75-3
Molecular Formula: C27H23N3O2
Molecular Weight: 421.499
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: 2,4(1H,3H)-Pyrimidinedione, 5-(6H-cyclohepta[b]naphthalen-6-yl)-1,3-dimethyl-6-(phenylamino)-(CAS DataBase Reference)
NIST Chemistry Reference: 2,4(1H,3H)-Pyrimidinedione, 5-(6H-cyclohepta[b]naphthalen-6-yl)-1,3-dimethyl-6-(phenylamino)-(874461-75-3)
EPA Substance Registry System: 2,4(1H,3H)-Pyrimidinedione, 5-(6H-cyclohepta[b]naphthalen-6-yl)-1,3-dimethyl-6-(phenylamino)-(874461-75-3)

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: 874461-75-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 874461-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,4,6 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 874461-75:
(8*8)+(7*7)+(6*4)+(5*4)+(4*6)+(3*1)+(2*7)+(1*5)=203
203 % 10 = 3
So 874461-75-3 is a valid CAS Registry Number.

874461-75-3Upstream product

874461-75-3Downstream Products

874461-75-3Relevant academic research and scientific papers

Synthesis, properties, and oxidizing ability of areno-annulated 1,3-dimethyl-10-phenylcyclohepta[4,5]pyrrolo[2,3-d]pyrimidine-2,4(1,3H) -dionylium ions

Naya, Shin-Ichi,Ohtoshi, Hiroshi,Nitta, Makoto

, p. 176 - 184 (2006)

Novel areno-annulated 1,3-dimethyl-10-phenylcyclohepta[4,5]pyrrolo[2,3-d] pyrimidine-2,4(1,3H)-dionylium ions 12a,b+·BF4 - and 16a+-BF4- were synthesized by three-step reactions, starting f

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