Zacopride

Base Information

• Chemical Name: Zacopride
• CAS No.: 90182-92-6
• Molecular Formula: C15H20ClN3O2
• Molecular Weight: 309.796
• UNII: 9GN3OT4156
• DSSTox Substance ID: DTXSID1048251
• Nikkaji Number: J22.809E
• Wikipedia: Zacopride
• Wikidata: Q75830
• NCI Thesaurus Code: C152942
• Pharos Ligand ID: XW48XGX4Q6RM
• ChEMBL ID: CHEMBL18041
• Mol file: 90182-92-6.mol

Synonyms:4-amino-5-iodo-2-methoxy-N-(1-azabicyclo(2.2.2)oct-3-yl)benzamide;4-amino-N-(1-azabicyclo(2,2,2)oct-3-yl)-5-chloro-2-methoxybenzamide-2-butenedioate;iodozacopride;zacopride;zacopride hydrochloride

Chemical Property of Zacopride

Chemical Property:

• Vapor Pressure: 1.61E-08mmHg at 25°C
• Boiling Point: 456.5°Cat760mmHg
• Flash Point: 229.9°C
• PSA: 67.59000
• Density: 1.33g/cm³
• LogP: 2.66480
• Storage Temp.: Desiccate at RT
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 309.1244046
• Heavy Atom Count: 21
• Complexity: 387

Purity/Quality:

99% ^*data from raw suppliers

Zacopride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC(=C(C=C1C(=O)NC2CN3CCC2CC3)Cl)N
• Uses: Anti-emetic; stimulant (peristaltic). Zacopride is a highly potent SR-3 antagonist and SR-4 agonist. 5-HT3 receptor antagonist. Activates IK1 channel.
• Therapeutic Function: Antiemetic, Peristaltic stimulant

Technology Process of Zacopride

There total 1 articles about Zacopride 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:

→ zacopride (90182-92-6)

Guidance literature:

Reference yield:

zacopride (90182-92-6) → 4-Amino-N-(1-azabicyclo[2.2.2.]oct-3-yl)-5-chloro-2-hydroxybenzamide (120713-17-9)

Guidance literature:

With ethanethiol; In water; N,N-dimethyl-formamide;

Reference yield:

ammonium hydroxide (1336-21-6) + zacopride (90182-92-6) → 4-Amino-N-(1-azabicyclo[2.2.2]oct-3-yl)-5-chloro-2-hydroxybenzamide, hydrochloride (120713-29-3)

Guidance literature:

With hydrogenchloride; boron tribromide; In dichloromethane; water;

Downstream raw materials:

4-Amino-N-(1-azabicyclo[2.2.2]oct-3-yl)-5-chloro-2-hydroxybenzamide, hydrochloride

4-Amino-N-(1-azabicyclo[2.2.2.]oct-3-yl)-5-chloro-2-hydroxybenzamide

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