150681-95-1

Basic information

• Product Name: (Methyl-{1-[4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}-amino)-acetic acid ethyl ester
• Synonyms: (Methyl-{1-[4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}-amino)-acetic acid ethyl ester
• CAS NO: 150681-95-1
• Molecular Weight: 499.61
• Mol File: 150681-95-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (Methyl-{1-[4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}-amino)-acetic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (Methyl-{1-[4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}-amino)-acetic acid ethyl ester(150681-95-1)
• EPA Substance Registry System: (Methyl-{1-[4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}-amino)-acetic acid ethyl ester(150681-95-1)

Safety Data

• Hazardous Substances Data: 150681-95-1(Hazardous Substances Data)

Upstream product

• 105-36-2 ethyl bromoacetate 
• 154890-02-5 5-methylamino-1-[4-[(2-methylbenzoyl)amino]benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine 
• 137976-61-5 2-methyl-4'-[(5-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl)carbonyl]benzanilide 
• 137975-89-4 1-(4-nitrobenzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one 
• 137976-09-1 1-(4-aminobenzoyl)-2,3,4,5-tetrahydro1H-1-benzazepin-5-one 
• 122-04-3 4-nitro-benzoyl chloride 
• 1127-74-8 1,2,3,4-tetrahydro-5H-benzo[b] azepin-5-one 

Relevant articles and documents

Orally active, nonpeptide vasopressin V2 receptor antagonists: A novel series of 1-[4-(benzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepines and related compounds

This paper describes a novel series of nonpeptide vasopressin V2 receptor antagonists. It has been demonstrated that the 1-[4- (benzoylamino)benzoyl]-2,3,4,5-1H-benzazepines and 1-[4- (benzoylamino)benzoyl]-2,3,4,5-1H-1,5-benzodiazepines show a high affinity for V2 (and V(1a)) receptors. Among the 1-[4-(benzoylamino)benzoyl]-2,3,4,5- 1H-benzazepine series, compounds with an alkylamino group on the benzazepine ring have been shown to have oral activity. A lipophilic group at the ortho position on the terminal benzoyl ring is important for both high V2 receptor affinity and oral activity. On the basis of these favorable properties, clinical testing of 31b has begun for use as an oral and iv aquaretic agent.