Cisapride monohydrate - ≥99% , CAS No.260779-88-2

CAS: 260779-88-2 Cat. No.: C346766 Formula: C₂₃H₂₉N₃O₄ClF • H₂O Peso molecolare: 483.96 Numero EC: 623-862-5 PubChem CID: 13677778

GRADE & PURITY ≥99%

Synonyms

4-AMINO-5-CHLORO-N-((3R,4S)-1-(3-(4-FLUOROPHENOXY)PROPYL)-3-METHOXYPIPERIDIN-4-YL)-2-METHOXYBENZAMIDE HYDRATE | 4-amino-5-chloro-N-[(3R,4S)-1-[3-(4-fluorophenoxy)propyl]-3-methoxypiperidin-4-yl]-2-methoxybenzamide;hydrate | F20664 | SCHEMBL9721799 | QBYYX

Storage

Room temperature,Argon charged

Shipped In

Normal

Panoramica

5-HT4 serotonin receptor agonist

Specifications

Sinonimi

4-AMINO-5-CHLORO-N-((3R,4S)-1-(3-(4-FLUOROPHENOXY)PROPYL)-3-METHOXYPIPERIDIN-4-YL)-2-METHOXYBENZAMIDE HYDRATE | 4-amino-5-chloro-N-[(3R,4S)-1-[3-(4-fluorophenoxy)propyl]-3-methoxypiperidin-4-yl]-2-methoxybenzamide;hydrate | F20664 | SCHEMBL9721799 | QBYYX

Specifiche e purezza

≥99%

Meccanismi biochimici e fisiologici

5-HT4 serotonin receptor agonist.

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

Normal

Purezza

≥99%

Nomi e identificatori

• Pubchem Sid: 488198503
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488198503
• Sorrisi canonici: COC1CN(CCC1NC(=O)C2=CC(=C(C=C2OC)N)Cl)CCCOC3=CC=C(C=C3)F.O
• IUPAC Name: 4-amino-5-chloro-N-[(3R,4S)-1-[3-(4-fluorophenoxy)propyl]-3-methoxypiperidin-4-yl]-2-methoxybenzamide;hydrate
• InChIKey: QBYYXIDJOFZORM-IKGOIYPNSA-N
• INCHI: 1S/C23H29ClFN3O4.H2O/c1-30-21-13-19(26)18(24)12-17(21)23(29)27-20-8-10-28(14-22(20)31-2)9-3-11-32-16-6-4-15(25)5-7-16;/h4-7,12-13,20,22H,3,8-11,14,26H2,1-2H3,(H,27,29);1H2/t20-,22+;/m0./s1
• Isomeri SMILES: CO[C@@H]1CN(CC[C@@H]1NC(=O)C2=CC(=C(C=C2OC)N)Cl)CCCOC3=CC=C(C=C3)F.O
• WGK Germania: 2
• RTECS: CU9372000
• CAS alternativo: 81098-60-4
• PubChem CID: 13677778
• Peso molecolare: 483.96

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzoic acids and derivatives
        • Level5 Aminobenzoic acids and derivatives
          • Level6 Aminobenzamides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzoic acids and derivatives
• Intermediate Tree Nodes: Aminobenzoic acids and derivatives
• Direct Parent: Aminobenzamides
• Alternative Parents: 3-halobenzoic acids and derivatives Aminophenyl ethers Benzamides Methoxyanilines Anisoles Phenoxy compounds Benzoyl derivatives Methoxybenzenes Alkyl aryl ethers Chlorobenzenes Fluorobenzenes Piperidines Aryl chlorides Aryl fluorides Amino acids and derivatives Secondary carboxylic acid amides Trialkylamines Azacyclic compounds Dialkyl ethers Organochlorides Organofluorides Primary amines Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Aminobenzamide - Benzamide - Aminophenyl ether - Methoxyaniline - Benzoyl - Phenol ether - Phenoxy compound - Aniline or substituted anilines - Anisole - Methoxybenzene - Chlorobenzene - Fluorobenzene - Halobenzene - Alkyl aryl ether - Aryl halide - Piperidine - Aryl fluoride - Aryl chloride - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Organofluoride - Organonitrogen compound - Organooxygen compound - Primary amine - Amine - Organic nitrogen compound - Organic oxygen compound - Organochloride - Organic oxide - Hydrocarbon derivative - Organohalogen compound - Aromatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as aminobenzamides. These are organic compounds containing a benzamide moiety with an amine group attached to the benzene ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in DMSO
• Sensibilità: Moisture sensitive.
• Punto di fusione (°C): 110°C (lit.)
• Peso molecolare: 484.000 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 9
• Exact Mass: 483.194 Da
• Monoisotopic Mass: 483.194 Da
• Topological Polar Surface Area: 87.100 Ų
• Heavy Atom Count: 33
• Formal Charge: 0
• Complexity: 581.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3