Cas no 2228725-60-6 (O-(1-methylcyclohexyl)methylhydroxylamine)

O-(1-Methylcyclohexyl)methylhydroxylamine is a specialized hydroxylamine derivative featuring a 1-methylcyclohexylmethyl substituent. This compound is of interest in synthetic organic chemistry due to its potential as a versatile intermediate in the preparation of N-alkylated hydroxylamines, oximes, and other nitrogen-containing functional groups. The sterically hindered cyclohexyl moiety may enhance stability and selectivity in certain reactions, making it useful for controlled functionalization. Its structure also suggests applicability in asymmetric synthesis or as a protecting group for carbonyl compounds. The compound’s reactivity can be tailored for use in pharmaceuticals, agrochemicals, or materials science, where precise nitrogen incorporation is required. Handling should follow standard safety protocols for hydroxylamine derivatives.
O-(1-methylcyclohexyl)methylhydroxylamine structure
2228725-60-6 structure
Product Name:O-(1-methylcyclohexyl)methylhydroxylamine
CAS No:2228725-60-6
MF:C8H17NO
MW:143.226682424545
CID:5850095
PubChem ID:145674276
Update Time:2025-05-20

O-(1-methylcyclohexyl)methylhydroxylamine Chemical and Physical Properties

Names and Identifiers

    • O-(1-methylcyclohexyl)methylhydroxylamine
    • O-[(1-methylcyclohexyl)methyl]hydroxylamine
    • EN300-1782441
    • 2228725-60-6
    • Inchi: 1S/C8H17NO/c1-8(7-10-9)5-3-2-4-6-8/h2-7,9H2,1H3
    • InChI Key: QDFGXYMUPKXGEM-UHFFFAOYSA-N
    • SMILES: O(CC1(C)CCCCC1)N

Computed Properties

  • Exact Mass: 143.131014166g/mol
  • Monoisotopic Mass: 143.131014166g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 97.4
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.1
  • Topological Polar Surface Area: 35.2?2

O-(1-methylcyclohexyl)methylhydroxylamine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Enamine
EN300-1782441-0.05g
O-[(1-methylcyclohexyl)methyl]hydroxylamine
2228725-60-6
0.05g
$780.0 2023-09-20
Enamine
EN300-1782441-0.1g
O-[(1-methylcyclohexyl)methyl]hydroxylamine
2228725-60-6
0.1g
$817.0 2023-09-20
Enamine
EN300-1782441-0.25g
O-[(1-methylcyclohexyl)methyl]hydroxylamine
2228725-60-6
0.25g
$855.0 2023-09-20
Enamine
EN300-1782441-0.5g
O-[(1-methylcyclohexyl)methyl]hydroxylamine
2228725-60-6
0.5g
$891.0 2023-09-20
Enamine
EN300-1782441-1.0g
O-[(1-methylcyclohexyl)methyl]hydroxylamine
2228725-60-6
1g
$928.0 2023-06-03
Enamine
EN300-1782441-2.5g
O-[(1-methylcyclohexyl)methyl]hydroxylamine
2228725-60-6
2.5g
$1819.0 2023-09-20
Enamine
EN300-1782441-5.0g
O-[(1-methylcyclohexyl)methyl]hydroxylamine
2228725-60-6
5g
$2692.0 2023-06-03
Enamine
EN300-1782441-10.0g
O-[(1-methylcyclohexyl)methyl]hydroxylamine
2228725-60-6
10g
$3992.0 2023-06-03
Enamine
EN300-1782441-1g
O-[(1-methylcyclohexyl)methyl]hydroxylamine
2228725-60-6
1g
$928.0 2023-09-20
Enamine
EN300-1782441-5g
O-[(1-methylcyclohexyl)methyl]hydroxylamine
2228725-60-6
5g
$2692.0 2023-09-20

Additional information on O-(1-methylcyclohexyl)methylhydroxylamine

Introduction to O-(1-methylcyclohexyl)methylhydroxylamine and Its Applications

O-(1-methylcyclohexyl)methylhydroxylamine (CAS No: 2228725-60-6) is a specialized organic compound that has garnered significant attention in the field of chemical and pharmaceutical research. This compound, characterized by its unique structural and functional properties, plays a crucial role in various scientific applications, particularly in the development of novel therapeutic agents and biochemical research.

The molecular structure of O-(1-methylcyclohexyl)methylhydroxylamine consists of a hydroxylamine moiety linked to a 1-methylcyclohexyl group. This configuration imparts distinctive chemical reactivity and stability, making it a valuable intermediate in synthetic chemistry. The compound's ability to participate in nucleophilic substitution reactions and its compatibility with a range of organic solvents enhance its utility in laboratory settings.

In recent years, O-(1-methylcyclohexyl)methylhydroxylamine has been explored for its potential applications in drug discovery and development. Its structural features make it a promising candidate for synthesizing complex molecules that exhibit pharmacological activity. Researchers have leveraged its reactivity to develop novel intermediates for antiviral, anti-inflammatory, and anticancer agents. The compound's ability to undergo selective functionalization has opened new avenues for designing targeted therapies with improved efficacy and reduced side effects.

One of the most compelling aspects of O-(1-methylcyclohexyl)methylhydroxylamine is its role in the synthesis of chiral compounds. The presence of the 1-methylcyclohexyl group introduces steric hindrance, which can be exploited to control the stereochemistry of reaction products. This is particularly important in pharmaceuticals, where the enantiomeric purity of drug candidates significantly influences their biological activity. The compound has been used to synthesize enantiomerically pure intermediates that serve as building blocks for next-generation therapeutics.

The chemical properties of O-(1-methylcyclohexyl)methylhydroxylamine also make it a valuable tool in biochemical research. Its reactivity with various functional groups allows researchers to probe reaction mechanisms and develop new synthetic methodologies. Additionally, the compound's stability under a range of conditions makes it suitable for long-term storage and repeated use in laboratory experiments. This reliability has made it a staple in many research groups studying organic synthesis and medicinal chemistry.

In the context of current research trends, O-(1-methylcyclohexyl)methylhydroxylamine has been incorporated into innovative strategies for drug development. For instance, its use in generating novel heterocyclic compounds has led to the discovery of new bioactive molecules with potential therapeutic applications. The compound's versatility has also been exploited in the design of catalytic systems that facilitate efficient synthetic transformations. These advancements highlight its importance as a key intermediate in modern chemical biology.

The synthesis of O-(1-methylcyclohexyl)methylhydroxylamine involves multi-step organic reactions that showcase the compound's synthetic utility. Researchers have developed efficient protocols for its preparation, ensuring high yields and purity levels suitable for pharmaceutical applications. The process typically involves the reaction of methyl hydroxylamine with 1-methylcyclohexanone or related derivatives under controlled conditions. These synthetic routes highlight the compound's accessibility and readiness for industrial-scale production.

The safety profile of O-(1-methylcyclohexyl)methylhydroxylamine is another critical consideration in its application. While it is not classified as a hazardous substance, proper handling procedures must be followed to ensure safe laboratory practices. Its compatibility with standard organic solvents and reagents makes it relatively easy to handle, but precautions such as using personal protective equipment (PPE) are essential when working with any chemical compound.

The future prospects of O-(1-methylcyclohexyl)methylhydroxylamine strong> are promising, with ongoing research exploring its potential in various fields. As drug discovery continues to evolve, this compound is expected to play an increasingly important role in developing innovative therapeutic solutions. Its unique chemical properties and synthetic versatility make it a cornerstone in modern medicinal chemistry and chemical biology.

Recommended suppliers
Shaanxi pure crystal photoelectric technology co. LTD
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Shaanxi pure crystal photoelectric technology co. LTD
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Zhejiang Brunova Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Zhejiang Brunova Technology Co., Ltd.
Hunan Well Medicine Synthesis Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hunan Well Medicine Synthesis Technology Co., Ltd.
HANGZHOU BAIS CHEMICAL TECHNOLOGY CO., LTD.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
HANGZHOU BAIS CHEMICAL TECHNOLOGY CO., LTD.