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Chlordiazepoxide hydrochloride

Base Information Edit
  • Chemical Name:Chlordiazepoxide hydrochloride
  • CAS No.:438-41-5
  • Molecular Formula:C16H14 Cl N3 O . Cl H
  • Molecular Weight:336.221
  • Hs Code.:2933910000
  • European Community (EC) Number:207-117-8
  • NSC Number:115748
  • UNII:MFM6K1XWDK
  • Wikidata:Q27106148
  • NCI Thesaurus Code:C47973
  • RXCUI:203173
  • ChEMBL ID:CHEMBL1200703
  • Mol file:438-41-5.mol
Chlordiazepoxide hydrochloride

Synonyms:7 Chloro 2 methylamino 5 phenyl 3H 1,4 benzodiazepine 4 oxide;7 Chloro N methyl 5 phenyl 3H 1,4 benzodiazepin 2 amine 4 oxide;7-chloro-2-methylamino-5-phenyl-3H-1,4-benzodiazepine-4-oxide;7-Chloro-N-methyl-5-phenyl-3H-1,4-benzodiazepin-2-amine 4-oxide;Chlordiazepoxide;Chlordiazepoxide Hydrobromide;Chlordiazepoxide Hydrochloride;Chlordiazepoxide Monohydrochloride;Chlordiazepoxide Perchlorate;Chlozepid;Elenium;Hydrobromide, Chlordiazepoxide;Hydrochloride, Chlordiazepoxide;Librium;Methaminodiazepoxide;Monohydrochloride, Chlordiazepoxide;Perchlorate, Chlordiazepoxide

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Chemical Property of Chlordiazepoxide hydrochloride Edit
Chemical Property:
  • Appearance/Colour:white crystalline powder 
  • Vapor Pressure:3.78E-13mmHg at 25°C 
  • Melting Point:212 - 218 C 
  • Boiling Point:451°Cat760mmHg 
  • Flash Point:226.6°C 
  • PSA:53.14000 
  • Density:g/cm3 
  • LogP:3.53800 
  • Solubility.:Soluble in water, sparingly soluble in ethanol (96 per cent). 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:335.0592175
  • Heavy Atom Count:22
  • Complexity:580
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn 
  • Statements: 22-62-63-68 
  • Safety Statements: 22-36/37 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CN=C1CN(C(=C2C=C(C=CC2=N1)Cl)C3=CC=CC=C3)O.Cl
  • Uses Sedative-hypnotic.
  • Therapeutic Function Tranquilizer
  • Clinical Use #N/A
  • Drug interactions Potentially hazardous interactions with other drugs Antibacterials: metabolism possibly increased by rifampicin. Antipsychotics: enhanced sedative effects; serious adverse events reported with clozapine and benzodiazepines. Antivirals: concentration possibly increased by ritonavir. Sodium oxybate: enhanced effects of sodium oxybate - avoid. Ulcer-healing drugs: metabolism inhibited by cimetidine.
Technology Process of Chlordiazepoxide hydrochloride

There total 2 articles about Chlordiazepoxide hydrochloride 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:
Guidance literature:
With hydrogenchloride; In acetone; at 50 - 60 ℃; for 4.5h; Time; Solvent;
Guidance literature:
aus II;
DOI:10.1002/ardp.19723050208
Refernces Edit