2-Aminoheptane - 10mM in DMSO , CAS No.123-82-0

CAS: 123-82-0 Cat. No.: A421028 Formule: C₇H₁₇N Poids moléculaire: 115.22 Beilstein Registry Number: 635676 Numéro CE: 204-655-5

GRADE & PURITY 10mM in DMSO

Synonyms

2-AMINOHEPTANE|tuaminoheptane|123-82-0|2-Heptylamine|2-Heptanamine|heptan-2-amine|1-Methylhexylamine|Heptamine|Tuamine|Heptin|Heptedrine|Tuaminoheptan|Rineptil|Rineptyl|Methyl-n-hexylamine|Armeen L-7|Tuaminoheptanum|Tuaminoheptanez|Hexylamine, 1-methyl-|(

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Synonymes

2-AMINOHEPTANE | tuaminoheptane | 123-82-0 | 2-Heptylamine | 2-Heptanamine | heptan-2-amine | 1-Methylhexylamine | Heptamine | Tuamine | Heptin | Heptedrine | Tuaminoheptan | Rineptil | Rineptyl | Methyl-n-hexylamine | Armeen L-7 | Tuaminoheptanum | Tuaminoheptanez | Hexylamine, 1-methyl- | (

Spécifications et pureté

10mM in DMSO

Conditions de stockage de stockage

Store at -80°C

Expédié en

Dry ice packs + Cold packs

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Noms et identifiants

• Pubchem Sid: 528756722
• Sourires canoniques: CCCCCC(C)N
• IUPAC Name: heptan-2-amine
• InChIKey: VSRBKQFNFZQRBM-UHFFFAOYSA-N
• INCHI: 1S/C7H17N/c1-3-4-5-6-7(2)8/h7H,3-6,8H2,1-2H3
• Isomères SMILES: CCCCCC(C)N
• WGK Allemagne: 3
• RTECS: MQ5425000
• Poids moléculaire: 115.22
• Beilstein: 635676
• Reaxy-Rn: 635676
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635676&ln=

Taxonomic Classification

Taxonomy Tree

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

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

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Cibles associées (non humaines)

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Discover Target: Hdac6

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Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Light sensitive;Air sensitive
• Indice de réfraction: 1.418
• Point d'éclair (°F): 91°F
• Point d'éclair (°C): 33 °C
• Poids moléculaire: 115.220 g/mol
• XLogP3: 2.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 115.136 Da
• Monoisotopic Mass: 115.136 Da
• Topological Polar Surface Area: 26.000 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 43.700
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Références

1. Xiaoyao Fei, Shaoyun Chen, Chunjie Huang, Dai Liu, Yongchun Zhang.  (2015)  Immobilization of bovine carbonic anhydrase on glycidoxypropyl-functionalized nanostructured mesoporous silicas for carbonation reaction.  JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC,      [PMID:] [10.1016/j.molcatb.2015.03.016]