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

CAS: 765-30-0 Cat. No.: C108049 Summenformel: C₃H₇N Molekulargewicht: 57.09 Beilstein Registry Number: 741858 EG-Nummer: 212-142-2

QUALITÄT & REINHEIT ≥98%

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Übersicht

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

Spezifikationen

Spezifikationen & Reinheit

≥98%

Biochemische und physiologische Mechanismen

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

Storage

Room temperature,Argon charged,Desiccated

Verschickt in

Normal

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

504754448

Pubchem Sid Url

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

Kanonisches Lächeln

C1CC1N

IUPAC Name

cyclopropanamine

InChIKey

HTJDQJBWANPRPF-UHFFFAOYSA-N

INCHI

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

Isomere SMILES

C1CC1N

WGK Deutschland

2

RTECS

GZ0685500

UN-Nummer

2733

Molekulargewicht

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
    • Klasse Organonitrogen compounds
      • Subclass Amines
        • Ebene5 Primary amines
          • Ebene6 Monoalkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Löslichkeit: Miscible with water, ethanol,ether and chloroform.
• Empfindlichkeit: air sensitive;Hygroscopic
• Brechungsindex: 1.42
• Flammpunkt (°F): 33.8 °F
• Flammpunkt (°C): -26 °C
• Siedepunkt (°C): 49-50°C
• Schmelzpunkt (°C): -10 °C
• Molekulargewicht: 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