Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Benzotript

Base Information Edit
  • Chemical Name:Benzotript
  • CAS No.:39544-74-6
  • Molecular Formula:C18H14ClN2O3-
  • Molecular Weight:342.782
  • Hs Code.:2933990090
  • European Community (EC) Number:254-500-0
  • UNII:LS5O682BRO
  • DSSTox Substance ID:DTXSID501043305
  • Nikkaji Number:J16.632D
  • Wikidata:Q27283157
  • NCI Thesaurus Code:C76479
  • ChEMBL ID:CHEMBL63544
  • Mol file:39544-74-6.mol
Benzotript

Synonyms:benzotript;benzotripte;N-(4-chlorobenzoyl)-L-tryptophan

Suppliers and Price of Benzotript
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Benzotript
  • 100mg
  • $ 815.00
  • American Custom Chemicals Corporation
  • (2S)-2-[(4-CHLOROBENZOYL)AMINO]-3-(1H-INDOL-3-YL)PROPANOIC ACID 95.00%
  • 100MG
  • $ 307.65
Total 6 raw suppliers
Chemical Property of Benzotript Edit
Chemical Property:
  • Vapor Pressure:1.88E-17mmHg at 25°C 
  • Boiling Point:643.7°C at 760 mmHg 
  • Flash Point:343.1°C 
  • PSA:82.19000 
  • LogP:3.63790 
  • Storage Temp.:-20°C 
  • Solubility.:Soluble in DMSO (up to at least 25 mg/ml) 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:342.0771200
  • Heavy Atom Count:24
  • Complexity:465
Purity/Quality:

98%Min *data from raw suppliers

Benzotript *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)NC(=O)C3=CC=C(C=C3)Cl
  • Isomeric SMILES:C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)O)NC(=O)C3=CC=C(C=C3)Cl
  • Description Benzotript (39544-74-6) antagonizes the interaction of cholecystokinin and related peptides with the cholecystokinin receptor.1 ?It has been reported to potentiate morphine analgesia via interaction with opioid receptors.2
Technology Process of Benzotript

There total 4 articles about Benzotript 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: 87.0%

Guidance literature:
Guidance literature:
4-chloro-benzoyl chloride; L-Tryptophan; With sodium hydroxide; In water; at 20 ℃; for 3h;
With hydrogenchloride; In water; pH=1 - 2;
DOI:10.1039/c3ob40215k
Guidance literature:
Nα-Fmoc-Nim-tert-butyloxycarbonyl-L-tryptophan 4-hydroxymethylphenoxy resin; With piperidine; In N,N-dimethyl-formamide; at 20 ℃;
para-chlorobenzoic acid; With benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 2h;
With methoxybenzene; trifluoroacetic acid; at 20 ℃; for 1h;
DOI:10.1016/j.bmcl.2004.02.046
Post RFQ for Price