9-Aminophenanthrene - ≥97% , CAS No.947-73-9

CAS: 947-73-9 Cat. No.: A350288 Summenformel: C₁₄H₁₁N Molekulargewicht: 193.24 EG-Nummer: 213-431-6

GRADE & PURITY ≥97%

Synonyms

SY353453 | EINECS 213-431-6 | A845099 | 9AP | CHEBI:50475 | 9-PHENANTHRYLAMINE | AKOS015854888 | STR02251 | 9-Aminophenanthrene, 96% | DTXSID60241573 | Q27094313 | MFCD00001177 | 9-Aminophenanthrene | J-519490 | UNII-7M9M5KM2XY | BRN 2209422 | PD007045 |

Storage

Room temperature,Argon charged

Shipped In

Normal

Übersicht

Product Application：

9-Aminophenanthrene was used as a model ligand to study the binding of 9-aminophenanthrene to individual subsites within the active site of CYP(eryF).

Specifications

Synonyme

SY353453 | EINECS 213-431-6 | A845099 | 9AP | CHEBI:50475 | 9-PHENANTHRYLAMINE | AKOS015854888 | STR02251 | 9-Aminophenanthrene, 96% | DTXSID60241573 | Q27094313 | MFCD00001177 | 9-Aminophenanthrene | J-519490 | UNII-7M9M5KM2XY | BRN 2209422 | PD007045 |

Spezifikationen & Reinheit

≥97%

Storage

Room temperature,Argon charged

Verschickt in

Normal

Reinheit

≥97%

Namen und Kennungen

• Pubchem Sid: 488181890
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181890
• Kanonisches Lächeln: C1=CC=C2C(=C1)C=C(C3=CC=CC=C23)N
• IUPAC Name: phenanthren-9-amine
• InChIKey: KIHQWOBUUIPWAN-UHFFFAOYSA-N
• INCHI: 1S/C14H11N/c15-14-9-10-5-1-2-6-11(10)12-7-3-4-8-13(12)14/h1-9H,15H2
• Isomere SMILES: C1=CC=C2C(=C1)C=C(C3=CC=CC=C23)N
• WGK Deutschland: 3
• RTECS: SG0175000
• Molekulargewicht: 193.24
• Reaxy-Rn: 2209422
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2209422&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Phenanthrenes and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Phenanthrenes and derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenanthrenes and derivatives
• Alternative Parents: Naphthalenes Primary amines Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Phenanthrene - Naphthalene - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic homopolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.
• External Descriptors: phenanthrenamine

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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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: air sensitive
• Schmelzpunkt (°C): 137-139 °C
• Molekulargewicht: 193.240 g/mol
• XLogP3: 3.700
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 193.089 Da
• Monoisotopic Mass: 193.089 Da
• Topological Polar Surface Area: 26.000 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 225.000
• 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

1. Jiexiang Tong, Subin Xie, Jia-Tao Miao, Jing Luo, Ren Liu.  (2023)  A novel method to synthesize polyurethane-urea acrylate with high strength and toughness.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2023.108006]

2. Zexin Liu, Xin Zhang, Cai Liu, Dongyang Li, Miaoxin Zhang, Fuxing Yin, Guoqing Xin, Gongkai Wang.  (2020)  Ferroconcrete-inspired design of a nonwoven graphene fiber fabric reinforced electrode for flexible fast-charging sodium ion storage devices.  Journal of Materials Chemistry A,  8  (5): (2777-2788).  [PMID:] [10.1039/C9TA12770D]

3. Yu Guan, Jiang Wu, Yuyu Lin, Qizhen Liu, Yongfen Qi, Weiguo Pan, Ping He, Xuemei Qi, Run Wang, Zhonghao Ji.  (2019)  Solvent-exfoliation of transition-metal dichalcogenide MoS2 to provide more active sites for enhancing photocatalytic performance of BiOIO3/g-C3N4 photocatalyst.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2019.03.177]

4. Huie Jiang, Lin Yang, Haiyan Ju, Lanxue Zou, Tianqi Zhao, Peng Guo, Qian Zhang, Haijiao Xie, Xinhua Liu.  (2025)  Ultralong-Lived and Color-Tunable RTP in Biodegradable Natural Fibers Based Textiles for Wearable Security and Display.  Small,      [PMID:41208399] [10.1002/smll.202511425]

5. Chenglong Ji, Jing Ma, Henggang Wang, Song Liu, Yu-e Shi, Peng Zhang, Zhenguang Wang.  (2025)  Efficient Visible Light Activated Afterglow Through Stabilizing Excited Dimers Via a Melt-Injection Reaction for Multiple Applications.  Advanced Optical Materials,      [PMID:] [10.1002/adom.202502328]

6. Haibo Li, Lei Yue, Hongxing Xu, Yanhong Li, Yining Zhou, Rong Zhang, Kongjie Wang, Hongzhong Zhang, Shuai Luo, Bin Ren, Fei Chen, Yufei Liu.  (2026)  A Poly-Aromatic Hydrocarbon-Grafted Silicon-Quantum-Dot-Based Desorption Agent with High Salt Resistance and Its Influence on the Adsorption/Desorption Behavior of CBM in Deep Coal Rock.  Polymers,  18  (7): (803).  [PMID:] [10.3390/polym18070803]