85012-73-3 Usage
General Description
1H-Imidazole-5-carboxaldehyde, 1-methyl-4-nitro- (9CI) is a chemical compound with the molecular formula C7H7N3O3. It is a nitro-substituted derivative of 1-methylimidazole and is commonly used in the synthesis of various pharmaceuticals and organic compounds. This chemical is known for its diverse range of applications, including as a building block in the production of unique organic molecules and as a reagent in biochemical assays. Additionally, it has been studied for its potential as a pharmaceutical compound with various bioactivities, such as antimicrobial and anti-inflammatory properties. Overall, 1H-Imidazole-5-carboxaldehyde, 1-methyl-4-nitro- (9CI) is an important compound with a wide range of uses in the fields of pharmaceuticals and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 85012-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,1 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85012-73:
(7*8)+(6*5)+(5*0)+(4*1)+(3*2)+(2*7)+(1*3)=113
113 % 10 = 3
So 85012-73-3 is a valid CAS Registry Number.
85012-73-3Relevant articles and documents
Synthesis and calcium channel antagonist activity of 1,4-dihydropyridine derivatives containing 4-nitroimidazolyl substituents
Shafiee, Abbas,Rastkary, Noushin,Jorjani, Masoumeh
, p. 537 - 542 (2007/10/03)
Alkyl, cycloalkyl and arylalkyl ester analogues of nifedipine (CAS 21829-25-4), in which the ortho-nitro phenyl group at position 4 is replaced by 1-methyl-4-nitro-5-imidazolyl substituent, were synthesized and evaluated as calcium channel antagonists usi
Synthesis of Some New Imidazole Derivatives
Ostrowski, S.
, p. 2237 - 2248 (2007/10/02)
N-Protected (CH2Ph, CH3) 4-nitroimidazoles (1) react with carbanions of tert-butyl chloroacetate, chloroacetonitrile and chloroform, affording Vicarious Nucleophilic Substitution of Hydrogen (VNS) products 2, 3, and 7, respectively.These compounds, after
