2-Methylcyclohexylamine - ≥98%, cantains 0.1%TBC as inbibitor , CAS No.7003-32-9

CAS: 7003-32-9 Cat. No.: M102224 Peso molecular: 113.2 Beilstein Registry Number: 2689073 Número EC: 230-277-5

GRADE & PURITY ≥98%, cantains 0.1%TBC as inbibitor

Synonyms

(1S,2S)-2-Methyl-cyclohexylamine | 2-methylcyclohexyl amine | AKOS000120118 | FT-0772786 | MFCD00001492 | NSC 27455 | 2methylcyclohexylamine | 2-METHYLCYCLOHEXYLAMINE | 2-methyl-cyclohexylamine | SB40025 | NSC27455 | NSC-27455 | o-Methylcyclohexylamine |

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

application：

2-Methylcyclohexylamine is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.

Specifications

Sinónimos

(1S, 2S)-2-Methyl-cyclohexylamine | 2-methylcyclohexyl amine | AKOS000120118 | FT-0772786 | MFCD00001492 | NSC 27455 | 2methylcyclohexylamine | 2-METHYLCYCLOHEXYLAMINE | 2-methyl-cyclohexylamine | SB40025 | NSC27455 | NSC-27455 | o-Methylcyclohexylamine |

Especificaciones y pureza

≥98%, cantains 0.1%TBC as inbibitor

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488182826
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488182826
• Sonrisas canónicas: CC1CCCCC1N
• IUPAC Name: 2-methylcyclohexan-1-amine
• InChIKey: FEUISMYEFPANSS-UHFFFAOYSA-N
• INCHI: 1S/C7H15N/c1-6-4-2-3-5-7(6)8/h6-7H,2-5,8H2,1H3
• Isómeros SMILES: CC1CCCCC1N
• WGK Alemania: 3
• Número ONU: 2733
• Peso molecular: 113.2
• Beilstein: 2689073
• Reaxy-Rn: 2689073
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2689073&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: 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
• Descripción: 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

Propiedades químicas y físicas

• Solubilidad: Slightly soluble in water.
• Sensibilidad: Air sensitive.
• Índice de refracción: 1.457
• Punto de inflamación (°F): 102.2 °F
• Punto de inflamación (°C): 21°C
• Punto de ebullición (°C): 147-149°C
• Peso molecular: 113.200 g/mol
• XLogP3: 1.600
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 113.12 Da
• Monoisotopic Mass: 113.12 Da
• Topological Polar Surface Area: 26.000 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 70.800
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 2
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Zhen He, Qiaohui Duan, Lingwen Liao, Chengming Wang.  (2023)  Surface strain-regulated twin-rich Au-Pt bimetallic nanowire for highly efficient alcohol oxidation reaction.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.143411]

2. Shichao Xu, Xiaojing Zeng, Songlin Dai, Jing Wang, Yuxiang Chen, Jie Song, Yunfei Shi, Xian Cheng, Shengliang Liao, Zhendong Zhao.  (2020)  Turpentine Derived Secondary Amines for Sustainable Crop Protection: Synthesis, Activity Evaluation and QSAR Study.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:32975941] [10.1021/acs.jafc.0c01909]

3. Jingkang Wang, Jinrui Wang, Xuyang Wang, Lei Tian, Zhendong Liu, Qin Lei, Dongzhi Wang, Jinrui Ye.  (2025)  Multifunctional analysis of novel aluminum-ion structural battery composites with optimization in cathode material.  COMPOSITES COMMUNICATIONS,      [PMID:] [10.1016/j.coco.2025.102410]

4. Zhen He, Chen Ma, Huangxu Li, Chengming Wang, Lingwen Liao.  (2025)  Twin Boundary-Regulated Platinum–Yttrium Elemental Distributions for Boosting Electrochemical Alcohol Oxidation.  ACS Applied Materials & Interfaces,      [PMID:40411828] [10.1021/acsami.5c06857]