Cyclopropylamine - ≥98% , CAS No.765-30-0

CAS: 765-30-0 Cat. No.: C108049 Fórmula: C₃H₇N Peso molecular: 57.09 Beilstein Registry Number: 741858 Número EC: 212-142-2

CALIDAD & PUREZA ≥98%

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Descripción general

Cyclopropylamine(CPA) has been used in the synthesis of N-[4-(4-fluoro)phenyl-2-aminothiazol-5-yl]pyrimidin-2-yl-alkylamine derivatives. It has been used in the synthesis of Pt(CPA)2(bismethylthiomethylenepropanedioate) and Pt(CPA)2(bisethylthiomethylenepropanedioate) complexes

Especificaciones

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

Cyclopropylamine inactivates cytochrome P450 enzymes by a mechanism involving initial one-electron oxidation at nitrogen followed by scission of the cyclopropane ring leading to covalent modification of the enzyme. It is a mechanism-based inhibitor of qui

Condiciones de almacenamiento de almacenamiento

Room temperature,Argon charged,Desiccated

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

Pubchem Sid

504754448

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504754448

Sonrisas canónicas

C1CC1N

IUPAC Name

cyclopropanamine

InChIKey

HTJDQJBWANPRPF-UHFFFAOYSA-N

INCHI

1S/C3H7N/c4-3-1-2-3/h3H,1-2,4H2

Isómeros SMILES

C1CC1N

WGK Alemania

2

RTECS

GZ0685500

Número ONU

2733

Peso molecular

57.09

Beilstein

741858

Reaxy-Rn

741858

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=741858&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amines
        • Level5 Primary amines
          • Level6 Monoalkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Primary amines
• Direct Parent: Monoalkylamines
• Alternative Parents: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Organopnictogen compound - Hydrocarbon derivative - Primary aliphatic amine - Aliphatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as monoalkylamines. These are organic compounds containing an primary aliphatic amine group.
• External Descriptors: a small molecule

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

Propiedades químicas y físicas

• Solubilidad: Miscible with water, ethanol,ether and chloroform.
• Sensibilidad: air sensitive;Hygroscopic
• Índice de refracción: 1.42
• Punto de inflamación (°F): 33.8 °F
• Punto de inflamación (°C): -26 °C
• Punto de ebullición (°C): 49-50°C
• Punto de fusión (°C): -10 °C
• Peso molecular: 57.090 g/mol
• XLogP3: 0.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 57.0578 Da
• Monoisotopic Mass: 57.0578 Da
• Topological Polar Surface Area: 26.000 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 22.500
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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: 1