158585-82-1 Usage
Derivative of imidazole and aldehyde
The compound is derived from imidazole (a five-membered ring with three nitrogen atoms) and aldehyde (a carbonyl group with at least one hydrogen atom attached).
Chemical structure
The structure of 1-METHYL-4-PHENYL-1H-IMIDAZOLE-5-CARBALDEHYDE consists of a five-membered imidazole ring with a methyl (CH3) and phenyl (C6H5) group attached to it.
Pharmaceutical applications
This compound has potential applications in the pharmaceutical industry, such as being used as a building block for the synthesis of other organic compounds.
Potential biological activities
1-METHYL-4-PHENYL-1H-IMIDAZOLE-5-CARBALDEHYDE may exhibit biological activities, making it a subject of research in medicinal chemistry.
Safety precautions
It is important to handle this chemical with care and follow safety guidelines to avoid any potential hazards or adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 158585-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,5,8 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 158585-82:
(8*1)+(7*5)+(6*8)+(5*5)+(4*8)+(3*5)+(2*8)+(1*2)=181
181 % 10 = 1
So 158585-82-1 is a valid CAS Registry Number.
158585-82-1Relevant articles and documents
THERAPEUTIC AGENTS
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Page 47, (2010/02/07)
A compound of the Formula: (I) (A chemical formula should be inserted here-please see paper copy enclosed herewith) Formula: (I); for use as a Tie2 receptor tyrosine kinase inhibitor in a warm-blooded animal such as man.
Carboxylate protection for the synthesis of 4,5-disubstituted 1-methylimidazoles
Shapiro,Gomez-Lor
, p. 5524 - 5526 (2007/10/02)
Using the carboxylate function as a readily removed blocking group for the 2-position, a regioselective synthesis of diverse 4,5-disubstituted 1-methylimidazoles has been developed starting from 1-methyltribromoimidazole, 5.
