Cas no 2164-19-4 (cis-2-methylcyclohexanamine)

Technical Introduction: cis-2-Methylcyclohexanamine cis-2-Methylcyclohexanamine is a chiral cyclohexylamine derivative characterized by its stereospecific cis-configuration. This compound is valued for its role as a versatile intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its rigid cyclohexane backbone and amine functionality enable selective reactivity in asymmetric synthesis and catalysis. The cis-configuration imparts distinct steric and electronic properties, making it useful for constructing complex molecular architectures. High purity grades are available to meet stringent application requirements. Proper handling under inert conditions is recommended due to its amine reactivity. This compound is typically supplied as a clear liquid or solid, depending on formulation.
cis-2-methylcyclohexanamine structure
cis-2-methylcyclohexanamine structure
Product Name:cis-2-methylcyclohexanamine
CAS No:2164-19-4
MF:C7H15N
MW:113.200701951981
MDL:MFCD06803062
CID:249893
PubChem ID:5324013
Update Time:2025-06-08

cis-2-methylcyclohexanamine Chemical and Physical Properties

Names and Identifiers

    • (1R,2S)-2-Methylcyclohexanamine
    • cis-2-methylcyclohexylamine
    • Cyclohexanamine,2-methyl-, (1R,2S)-rel-
    • 2-cis-Methylcyclohexanamine
    • cis-2-Methyl-1-cyclohexylamine
    • Cyclohexanamine,2-methyl-, cis-
    • Cyclohexylamine, 2-methyl-, cis- (8CI)
    • cis-2-Methyl-cyclohexylamine
    • cis-2-methylcyclohexanamine
    • CS-0058232
    • 2-Methylcyclohexylamine, cis-(+)-
    • EN300-6492337
    • (1R,2S)-(+)-cis-2-Methyl-cyclohexanamin
    • (1R,2S)-2-methylcyclohexan-1-amine
    • Q27236421
    • Cyclohexanamine, 2-methyl-, (1R-cis)-
    • FD10501
    • 79389-37-0
    • AKOS006285029
    • (1R,2S)-2-Methyl-cyclohexylamine
    • starbld0019577
    • SCHEMBL896134
    • 08OZI4NZZ2
    • Cyclohexanamine, 2-methyl-, (1R,2S)-
    • A864871
    • (1R,2S)-2-Methylcyclohexylamine
    • UNII-08OZI4NZZ2
    • 2-Methylcyclohexylamine, (1R,2S)-
    • MFCD18914324
    • 2164-19-4
    • cyclohexane, cis-1-amino-2-methyl-
    • DB-002971
    • DB-278462
    • MDL: MFCD06803062
    • Inchi: 1S/C7H15N/c1-6-4-2-3-5-7(6)8/h6-7H,2-5,8H2,1H3/t6-,7+/m0/s1
    • InChI Key: FEUISMYEFPANSS-NKWVEPMBSA-N
    • SMILES: N[C@@H]1CCCC[C@@H]1C

Computed Properties

  • Exact Mass: 113.12055
  • Monoisotopic Mass: 113.120449483g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 0
  • Complexity: 70.8
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 2
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.6
  • Topological Polar Surface Area: 26?2

Experimental Properties

  • Density: 0.844
  • Melting Point: -8.5°C (estimate)
  • Boiling Point: 154 oC
  • Flash Point: 22 oC
  • Refractive Index: 1.4688
  • PSA: 26.02
  • Vapor Pressure: 4.2±0.3 mmHg at 25°C

cis-2-methylcyclohexanamine Security Information

cis-2-methylcyclohexanamine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
JIE DA WEI ( SHANG HAI ) YI YAO KE JI FA ZHAN Co., Ltd.
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TRC
R701138-10mg
(1R,2S)-2-methylcyclohexan-1-amine
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$ 50.00 2022-06-02
TRC
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¥8726.45 2025-01-21

cis-2-methylcyclohexanamine Suppliers

Amadis Chemical Company Limited
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(CAS:2164-19-4)cis-2-methylcyclohexanamine
Order Number:A1031682
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Thursday, 29 August 2024 16:46
Price ($):556.0

Additional information on cis-2-methylcyclohexanamine

Introduction to cis-2-methylcyclohexanamine (CAS No. 2164-19-4)

Cis-2-methylcyclohexanamine (CAS No. 2164-19-4) is a versatile organic compound with significant applications in the fields of pharmaceuticals, chemical synthesis, and materials science. This compound is a chiral amine that plays a crucial role in the synthesis of various bioactive molecules and pharmaceutical intermediates. Its unique stereochemistry and chemical properties make it an essential building block in the development of novel drugs and materials.

The structure of cis-2-methylcyclohexanamine consists of a cyclohexane ring with a methyl group and an amine group attached to adjacent carbon atoms, forming a cis configuration. This configuration imparts specific physical and chemical properties that are highly valuable in synthetic chemistry. The compound is known for its high reactivity and selectivity, making it a preferred choice in asymmetric synthesis and catalysis.

Recent advancements in the field of medicinal chemistry have highlighted the importance of cis-2-methylcyclohexanamine in the development of new therapeutic agents. For instance, studies have shown that this compound can be used as a key intermediate in the synthesis of antiviral drugs, anti-inflammatory agents, and central nervous system (CNS) modulators. Its ability to form stable complexes with metal ions also makes it useful in coordination chemistry and the design of metal-based pharmaceuticals.

In the context of drug discovery, cis-2-methylcyclohexanamine has been utilized to enhance the bioavailability and efficacy of various drug candidates. Researchers have explored its potential as a prodrug moiety, where it can be selectively cleaved in vivo to release the active drug molecule. This approach has shown promise in improving the pharmacokinetic properties of drugs, particularly those with poor solubility or stability.

The synthetic methods for preparing cis-2-methylcyclohexanamine have been extensively studied and optimized over the years. Common approaches include asymmetric hydrogenation, enantioselective synthesis using chiral catalysts, and stereoselective transformations from readily available starting materials. These methods have enabled large-scale production of the compound with high enantiomeric purity, which is crucial for pharmaceutical applications.

In addition to its role in pharmaceuticals, cis-2-methylcyclohexanamine has found applications in other areas such as polymer science and materials engineering. Its ability to form hydrogen bonds and its amphiphilic nature make it useful as a surfactant or stabilizer in emulsion polymerization processes. It has also been used as a chiral additive in the preparation of chiral polymers and liquid crystals, which have potential applications in optical devices and sensors.

The environmental impact of cis-2-methylcyclohexanamine is another important consideration. Recent studies have focused on developing greener synthetic routes that minimize waste generation and reduce the use of hazardous reagents. These efforts align with the principles of green chemistry and sustainable manufacturing practices, ensuring that the production and use of this compound are environmentally responsible.

In conclusion, cis-2-methylcyclohexanamine (CAS No. 2164-19-4) is a multifaceted compound with a wide range of applications in pharmaceuticals, chemical synthesis, and materials science. Its unique stereochemistry and chemical properties make it an invaluable tool for researchers and chemists working on innovative solutions to complex problems. As research continues to advance, the potential uses of this compound are likely to expand further, contributing to advancements in various scientific fields.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:2164-19-4)cis-2-methylcyclohexanamine
A1031682
Purity:99%
Quantity:1g
Price ($):556.0
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