Cas 505061-18-7,2-[4-(2-benzyl-1H-benzimidazol-1-yl)butyl]-3-phenyl-2,3-dihydro-1,4-phthalazinedione

505061-18-7

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Basic information

Product Name: 2-[4-(2-benzyl-1H-benzimidazol-1-yl)butyl]-3-phenyl-2,3-dihydro-1,4-phthalazinedione
Synonyms: 2-[4-(2-benzyl-1H-benzimidazol-1-yl)butyl]-3-phenyl-2,3-dihydro-1,4-phthalazinedione
CAS NO:505061-18-7
Molecular Formula: C32H28N4O2
Molecular Weight: 500.59032
EINECS: N/A
Product Categories: N/A
Mol File: 505061-18-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-[4-(2-benzyl-1H-benzimidazol-1-yl)butyl]-3-phenyl-2,3-dihydro-1,4-phthalazinedione(CAS DataBase Reference)
NIST Chemistry Reference: 2-[4-(2-benzyl-1H-benzimidazol-1-yl)butyl]-3-phenyl-2,3-dihydro-1,4-phthalazinedione(505061-18-7)
EPA Substance Registry System: 2-[4-(2-benzyl-1H-benzimidazol-1-yl)butyl]-3-phenyl-2,3-dihydro-1,4-phthalazinedione(505061-18-7)

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: 505061-18-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 505061-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,5,0,6 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 505061-18:
(8*5)+(7*0)+(6*5)+(5*0)+(4*6)+(3*1)+(2*1)+(1*8)=107
107 % 10 = 7
So 505061-18-7 is a valid CAS Registry Number.

505061-18-7Upstream product

621-72-7 2-benzylbenzimidazole

505061-18-7Downstream Products

505061-18-7Relevant academic research and scientific papers

Studies on the syntheses of 1-substituted benzimidazole derivatives

Kowalska, Teresa,Kowalski, Piotr,Bojarski, Andrzej J.,Duszynska, Beata

, p. 361 - 366 (2007/10/03)

Several novel 1-heteroarylalkyl substituted benzimidazoles were synthesized in the reaction of various halogenoalkylheterocycles with benzimidazoles. The structures of the products were confirmed by their spectral and analytical data. The potential biolog

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