5-Amino-1-pentanol - ≥95% , CAS No.2508-29-4

CAS: 2508-29-4 Cat. No.: A107210 Summenformel: C₅H₁₃NO Molekulargewicht: 103.16 Beilstein Registry Number: 1732302 EG-Nummer: 219-718-2

GRADE & PURITY ≥95%

Synonyms

5-Amino-pentan-1-ol | 5-Aminopentan-1-ol | Tolmetin ?-D-Glucuronide | LQGKDMHENBFVRC-UHFFFAOYSA- | 1-amino-5-pentanol | 5-Amino-1-pentanol, 95% | Pentanol, 5-amino- | BP-13458 | 5-amino pentanol | 5-amino-l-pentanol | InChI=1/C5H13NO/c6-4-2-1-3-5-7/h7H,1-

Storage

Room temperature,Argon charged

Shipped In

Normal

Übersicht

5-Amino-1-pentanol undergoes facile intramolecular cyclocondensation with piperidine and methyl or ethyl piperidine in the presence of methanol or ethanol over zeolite catalys
Usually used in the synthesis of S-glycosyl amino-acid building blocks,and also has been used as starting reagent in the synthesis of aminofunctionalized 4-chloro-2,2′:6′,2′′-terpyridine.

Specifications

Synonyme

5-Amino-pentan-1-ol | 5-Aminopentan-1-ol | Tolmetin ?-D-Glucuronide | LQGKDMHENBFVRC-UHFFFAOYSA- | 1-amino-5-pentanol | 5-Amino-1-pentanol, 95% | Pentanol, 5-amino- | BP-13458 | 5-amino pentanol | 5-amino-l-pentanol | InChI=1/C5H13NO/c6-4-2-1-3-5-7/h7H,1-

Spezifikationen & Reinheit

≥95%

Storage

Room temperature,Argon charged

Verschickt in

Normal

Reinheit

≥95%

Namen und Kennungen

• Pubchem Sid: 488185146
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185146
• Kanonisches Lächeln: C(CCN)CCO
• IUPAC Name: 5-aminopentan-1-ol
• InChIKey: LQGKDMHENBFVRC-UHFFFAOYSA-N
• INCHI: 1S/C5H13NO/c6-4-2-1-3-5-7/h7H,1-6H2
• Isomere SMILES: C(CCN)CCO
• WGK Deutschland: 2
• UN-Nummer: 3259
• Molekulargewicht: 103.16
• Beilstein: 1732302
• Reaxy-Rn: 1732302
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1732302&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Klasse Organonitrogen compounds
      • Subclass Amines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Klasse: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkanolamines
• Alternative Parents: Primary alcohols Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkanolamine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as alkanolamines. These are organic compounds that carry a hydroxy and an amino functional groups on an alkane backbone.
• 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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Air Sensitive
• Gefrierpunkt (°C): 36 °C
• Brechungsindex: 1.4615
• Flammpunkt (°F): 150.8 °F
• Flammpunkt (°C): 65℃
• Siedepunkt (°C): 120-122°C
• Schmelzpunkt (°C): 34-37°C
• Molekulargewicht: 103.160 g/mol
• XLogP3: -0.300
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 103.1 Da
• Monoisotopic Mass: 103.1 Da
• Topological Polar Surface Area: 46.300 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 31.300
• 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

Referenzen

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