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

CAS: 123-82-0 Cat. No.: A421028 Summenformel: C₇H₁₇N Molekulargewicht: 115.22 Beilstein Registry Number: 635676 EG-Nummer: 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

Synonyme

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- | (

Spezifikationen & Reinheit

10mM in DMSO

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Namen und Kennungen

• Pubchem Sid: 528756722
• Kanonisches Lächeln: 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
• Isomere SMILES: CCCCCC(C)N
• WGK Deutschland: 3
• RTECS: MQ5425000
• Molekulargewicht: 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
    • 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 acyclic compounds
• Substituents: Organopnictogen compound - Hydrocarbon derivative - Primary aliphatic amine - Aliphatic acyclic 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: 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

Zugehörige Ziele (menschlich)

OPRM1 Tclin Mu-type opioid receptor (1 Activities)

Discover Target: OPRM1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

OPRM1 Tclin Mu opioid receptor (19785 Activities)

Discover Target: OPRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Zugehörige Ziele (nicht menschlich)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Light sensitive;Air sensitive
• Brechungsindex: 1.418
• Flammpunkt (°F): 91°F
• Flammpunkt (°C): 33 °C
• Molekulargewicht: 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

Referenzen

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]