Cas 908003-25-8,2-(4,5-dimethoxy-2-nitrophenyl)-4,5-bis-(4-methoxyphenyl)-1H-imidazole

908003-25-8

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Basic information

Product Name: 2-(4,5-dimethoxy-2-nitrophenyl)-4,5-bis-(4-methoxyphenyl)-1H-imidazole
Synonyms: 2-(4,5-dimethoxy-2-nitrophenyl)-4,5-bis-(4-methoxyphenyl)-1H-imidazole
CAS NO:908003-25-8
Molecular Formula:
Molecular Weight: 461.474
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-(4,5-dimethoxy-2-nitrophenyl)-4,5-bis-(4-methoxyphenyl)-1H-imidazole(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4,5-dimethoxy-2-nitrophenyl)-4,5-bis-(4-methoxyphenyl)-1H-imidazole(908003-25-8)
EPA Substance Registry System: 2-(4,5-dimethoxy-2-nitrophenyl)-4,5-bis-(4-methoxyphenyl)-1H-imidazole(908003-25-8)

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: 908003-25-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 908003-25-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,0,0 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 908003-25:
(8*9)+(7*0)+(6*8)+(5*0)+(4*0)+(3*3)+(2*2)+(1*5)=138
138 % 10 = 8
So 908003-25-8 is a valid CAS Registry Number.

908003-25-8Upstream product

908003-25-8Downstream Products

908003-29-2 2-[4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl]-4,5-dimethoxyphenylamine

908003-25-8Relevant academic research and scientific papers

Synthesis of a novel structural variant of imidazoquinazoline with three-point diversity

Sharma, Sunil,Saha, Biswajit,Sawant, Devesh,Kundu, Bijoy

, p. 1841 - 1847 (2006)

An efficient strategy for the preparation of a novel structural variant of imidazoquinazolines with three-point diversity has been described. The compounds were obtained by treating benzil with o-nitrobenzaldehyde to give imidazoles, followed by reduction

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