74115-04-1 Usage
Class
Benzazepine derivative
Structural Features
Chloro Group (6-position)
Methyl Group (3-position)
Phenyl Ring
Two Hydroxyl Groups (7and 8-positions)
Biological Activity
Chloro and methyl groups suggest potential biological activity due to their common occurrence in pharmacologically active compounds.
Presence of a phenyl ring further indicates potential pharmacological relevance.
Solubility
Presence of hydroxyl groups may influence the compound's solubility in aqueous and organic solvents.
Pharmacological Relevance
Further research is required to understand its pharmacological properties and potential applications.
Potential Applications
Due to its complex structure and benzazepine class, it may have potential pharmaceutical applications.
Research Requirement
Further research is necessary to fully elucidate its pharmacological properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 74115-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,1 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74115-04:
(7*7)+(6*4)+(5*1)+(4*1)+(3*5)+(2*0)+(1*4)=101
101 % 10 = 1
So 74115-04-1 is a valid CAS Registry Number.
74115-04-1Relevant academic research and scientific papers
6-HALO-3-LOWER ALKYL-7,8-DIHYDROXY-1-PHENYL-2,3,4,5-TETRAHYDRO-1H-3-BENZAZEPINES
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, (2008/06/13)
6-Halo-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines whose structures have a lower alkyl substituted at the 3 or N-position have potent and often specific anti-Parkinsonism activity by means of their central dopaminergic effect. The lead compound of the series is 6-chloro-3-methyl-1-phenyl-7,8-dihydroxy-2,3,4,5-tetrahydro-1H-3-benzazepin e as the base or its salts such as the hydrochloride, hydrobromide or methane sulfonate.
