Camazepam

Base Information

• Chemical Name: Camazepam
• CAS No.: 36104-80-0
• Deprecated CAS: 102818-69-9
• Molecular Formula: C19H18 Cl N3 O3
• Molecular Weight: 371.823
• European Community (EC) Number: 252-866-6
• UNII: HZ3XRH03C3
• DSSTox Substance ID: DTXSID50865803
• Nikkaji Number: J19.779C
• Wikipedia: Camazepam
• Wikidata: Q3651150
• NCI Thesaurus Code: C98123
• Metabolomics Workbench ID: 146144
• ChEMBL ID: CHEMBL1095282
• Mol file: 36104-80-0.mol

Synonyms:B 5833;B-5833;camazepam;S-58-33;SB 5833

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Chemical Property of Camazepam

Chemical Property:

• Vapor Pressure: 6.22E-13mmHg at 25°C
• Melting Point: 173-174°
• Refractive Index: 1.6470 (estimate)
• Boiling Point: 568.3°Cat760mmHg
• PKA: 2.21±0.50(Predicted)
• Flash Point: 297.5°C
• PSA: 62.21000
• Density: 1.29g/cm³
• LogP: 2.67870
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 371.1036691
• Heavy Atom Count: 26
• Complexity: 574

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN1C2=C(C=C(C=C2)Cl)C(=NC(C1=O)OC(=O)N(C)C)C3=CC=CC=C3
• Uses: Anxiolytic. Controlled substance (depressant).

Technology Process of Camazepam

There total 1 articles about Camazepam which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ Albego (36104-80-0)

Guidance literature:

Ester (2), (CH3)2NH;

Reference yield: 82.0%

chloroform (67-66-3,8013-54-5) + Albego (36104-80-0) → 8-chloro-1,9b-dihydro-3-(N,N-dimethylcarbamoyl)-5-methyl-9b-phenyl-3H-azirino<1,2-d><1,4>benzodiazepin-4(5H)-one

Guidance literature:

With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; Ambient temperature;

DOI:10.3987/COM-92-6143

Reference yield:

Albego (36104-80-0) → 5-chloro-2-aminobenzophenone (719-59-5)

Guidance literature:

With hydrogenchloride; multistep reaction: biotransformation, acid hydrolysis;

Downstream raw materials:

5-chloro-2-aminobenzophenone

5-chloro-2-(methylamino)benzophenone