Cas 1283135-30-7,1-(2-(4-chlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl)-2-methyl-4-nitro-1H-imidazole

1283135-30-7

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Basic information

Product Name: 1-(2-(4-chlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl)-2-methyl-4-nitro-1H-imidazole
Synonyms: 1-(2-(4-chlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl)-2-methyl-4-nitro-1H-imidazole
CAS NO:1283135-30-7
Molecular Formula:
Molecular Weight: 440.713
EINECS: N/A
Product Categories: N/A
Mol File: 1283135-30-7.mol
Article Data: 1

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: 1-(2-(4-chlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl)-2-methyl-4-nitro-1H-imidazole(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-(4-chlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl)-2-methyl-4-nitro-1H-imidazole(1283135-30-7)
EPA Substance Registry System: 1-(2-(4-chlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl)-2-methyl-4-nitro-1H-imidazole(1283135-30-7)

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: 1283135-30-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1283135-30-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,3,1,3 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1283135-30:
(9*1)+(8*2)+(7*8)+(6*3)+(5*1)+(4*3)+(3*5)+(2*3)+(1*0)=137
137 % 10 = 7
So 1283135-30-7 is a valid CAS Registry Number.

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1283135-30-7Relevant articles and documents

Synthesis and antitubercular activity of monocyclic nitroimidazoles: Insights from econazole

Lee, Sang-Ho,Kim, Suhyun,Yun, Min-Han,Lee, Yong Sup,Cho, Sang-Nae,Oh, Taegwon,Kim, Pilho

, p. 1515 - 1518 (2011/04/22)

We have designed and synthesized econazole-derived nitroimidazoles to investigate the antitubercular activity of the nitroimidazole compounds. The introduction of a nitro group at the 4-position of the imidazole on econazole abolished the antitubercular a

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