24111-57-7

Basic information

• Product Name: 5-Chloro-2-(β-hydroxypropylaminoacetylamino)benzophenone
• Synonyms: 5-Chloro-2-(β-hydroxypropylaminoacetylamino)benzophenone
• CAS NO: 24111-57-7
• Molecular Formula: C₁₈H₁₉ClN₂O₃
• Molecular Weight: 346.80806
• Mol File: 24111-57-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-Chloro-2-(β-hydroxypropylaminoacetylamino)benzophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Chloro-2-(β-hydroxypropylaminoacetylamino)benzophenone(24111-57-7)
• EPA Substance Registry System: 5-Chloro-2-(β-hydroxypropylaminoacetylamino)benzophenone(24111-57-7)

Safety Data

• Hazardous Substances Data: 24111-57-7(Hazardous Substances Data)

Upstream product

• 29912-93-4 oxazolam 
• 32580-26-0 2-(2-bromoacetamido)-5-chloro-benzophenone 
• 78-96-6 3-amino-2-propanol 
• 24143-17-7 oxazolam 

Downstream Products

• 24143-17-7 oxazolam 

Relevant articles and documents

The behavior of 1,4-benzodiazepine drugs in acidic media. V. Kinetics of hydrolysis of flutazolam and haloxazolam in aqueous solution

-

Intermediates for tricyclic benzodiazepines

Tricyclic benzodiazepine derivatives ("A") bearing a hydroxylower alkyl substituent in the 1-position and a heterocyclic ring joined between positions 4 and 5 of the benzodiazepine moiety are described. The heterocyclic ring will contain the nitrogen atom appearing at position 4 of the benzodiazepine ring as well as the hetero atom, which may be either oxygen or nitrogen, attached to the carbon atom at the 5-position of the benzodiazepine ring. "A" bearing an oxygen atom in the new heterocyclic ring may be formed from the corresponding 4,5-unsaturated benzodiazepines by treatment with an epoxide compound in the presence of an acid catalyst. "A" bearing either a nitrogen or an oxygen atom in the new heterocyclic ring may be prepared by cyclization of the corresponding open compound. "A" are useful as sedative, muscle relaxant and anti-convulsant agents.