cis-1,2-cicloesandiammina - ≥97% , CAS No.1436-59-5

CAS: 1436-59-5 Cat. No.: C153337 Formula: C₆H₁₄N₂ Peso molecolare: 114.19 Beilstein Registry Number: 13(4)5 Numero EC: 604-372-0

GRADE & PURITY ≥97%

Synonyms

cis-1,2-Cyclohexanediamine | R0ZN6K26EP | (R)(S)-1,2-Diaminocyclohexane | 1,2-Cyclohexanediamine,(1R,2S)-rel- | cis-cyclohexane-1,2-diamine | EN300-97199 | 1,2-Cis-diamino-cyclohexane | J-007850 | 1,2-Cyclohexanediamine, cis- | InChI=1/C6H14N2/c7-5-3-1-2-

Storage

Argon charged,Room temperature

Shipped In

Normale

Panoramica

Solitamente viene utilizzato nella sintesi di complessi di platino che hanno un'elevata attività antitumorale. È stato anche utilizzato nella sintesi di ligandi multidentati per la complessazione dell'uranile e dei metalli di transizione.

Specifications

Sinonimi

cis-1,2-Cyclohexanediamine | R0ZN6K26EP | (R)(S)-1,2-Diaminocyclohexane | 1,2-Cyclohexanediamine,(1R,2S)-rel- | cis-cyclohexane-1,2-diamine | EN300-97199 | 1,2-Cis-diamino-cyclohexane | J-007850 | 1,2-Cyclohexanediamine, cis- | InChI=1/C6H14N2/c7-5-3-1-2-

Specifiche e purezza

≥97%

Condizioni di conservazione di stoccaggio

Argon charged,Room temperature

Spedito in

Normale

Purezza

≥97%

Nomi e identificatori

• Pubchem Sid: 504758520
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504758520
• Sorrisi canonici: C1CCC(C(C1)N)N
• IUPAC Name: (1S,2R)-cyclohexane-1,2-diamine
• InChIKey: SSJXIUAHEKJCMH-OLQVQODUSA-N
• INCHI: 1S/C6H14N2/c7-5-3-1-2-4-6(5)8/h5-6H,1-4,7-8H2/t5-,6+
• Isomeri SMILES: C1CC[C@@H]([C@@H](C1)N)N
• Peso molecolare: 114.19
• Beilstein: 13(4)5
• Reaxy-Rn: 506142
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506142&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Cyclohexylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Cyclohexylamines
• Intermediate Tree Nodes: Not available
• Direct Parent: Cyclohexylamines
• Alternative Parents: Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Cyclohexylamine - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Amine - Aliphatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as cyclohexylamines. These are organic compounds containing a cyclohexylamine moiety, which consist of a cyclohexane ring attached to an 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

Proprietà chimiche e fisiche

• Solubilità: Water solubility: completely miscible
• Sensibilità: moisture & air & light sensitive
• Indice di rifrazione: 1.49
• Punto di infiammabilità (°F): 159.8 ℉(lit.)
• Punto di infiammabilità (°C): 71°C(lit.)
• Punto di ebollizione (°C): 93 °C/18 mmHg
• Peso molecolare: 114.190 g/mol
• XLogP3: -0.300
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 114.116 Da
• Monoisotopic Mass: 114.116 Da
• Topological Polar Surface Area: 52.000 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 62.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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

Riferimenti

1. Wu Jing, Zhi Yunfei, Shan Shaoyun, Su Hongying, Wu Shuisheng, Jia Qingming.  (2015)  Polypyrrole Nanofibers Supported Cr(III)(salen)Cl Catalyst: A Novel Polymer Supported Catalyst for Alternating Copolymerization of Cyclohexene Oxide with Carbon dioxide.  CATALYSIS LETTERS,  145  (10): (1913-1921).  [PMID:] [10.1007/s10562-015-1599-z]

2. Wei Yi, Zhang Yan, Li Yawen, Li Chen, Wang Yuxuan, Luo Zhishan, Liu Yulian, Kang Huimin, Chen Xihan, Quan Zewei.  (2025)  Chiral recognition via symmetry-dependent luminescence in zero-dimensional hybrid copper halides.  Nature Communications,  16  (1): (1-9).  [PMID:41038855] [10.1038/s41467-025-63835-y]