Cas no 55930-71-7 (Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl-)

Hydroxylamine, O-tricyclo[3.3.1.13,?]dec-1-yl-, is a specialized hydroxylamine derivative featuring a rigid adamantyl (tricyclo[3.3.1.13,?]decane) framework. This structural motif enhances steric hindrance and stability, making it useful in selective organic transformations, particularly in the synthesis of hindered oximes or as a protecting group in complex molecular architectures. The adamantyl group imparts improved solubility in organic solvents compared to conventional hydroxylamine derivatives, facilitating its application in non-polar reaction systems. Its unique reactivity profile allows for controlled functionalization in pharmaceutical and materials chemistry, where precise steric and electronic tuning is required. The compound is typically handled under inert conditions due to its potential sensitivity.
Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- structure
55930-71-7 structure
Product Name:Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl-
CAS No:55930-71-7
MF:C10H17NO
MW:167.248082876205
MDL:MFCD25964587
CID:4036822
PubChem ID:20319707
Update Time:2025-06-11

Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- Chemical and Physical Properties

Names and Identifiers

    • Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl-
    • O-(Adamantan-1-yl)hydroxylamine
    • CS-0088887
    • D74721
    • A1-20825
    • SCHEMBL1237993
    • SCHEMBL16199895
    • (O-adamantyl)hydroxylamine
    • O-(1-Adamantyl)hydroxylamine
    • 55930-71-7
    • CHEMBL2079062
    • MDL: MFCD25964587
    • Inchi: 1S/C10H17NO/c11-12-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6,11H2
    • InChI Key: LIGOOHYLYIIVMM-UHFFFAOYSA-N
    • SMILES: O(C12CC3CC(CC(C3)C1)C2)N

Computed Properties

  • Exact Mass: 167.131
  • Monoisotopic Mass: 167.131
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 161
  • 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
  • Topological Polar Surface Area: 35.2A^2
  • XLogP3: 2

Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Matrix Scientific
232282-2.500g
O-(Adamantan-1-yl)hydroxylamine, 95%
55930-71-7 95%
2.500g
$2063.00 2023-09-11
Chemenu
CM540650-1g
O-(Adamantan-1-yl)hydroxylamine
55930-71-7 95%+
1g
$*** 2023-05-30
AstaTech
D74721-0.25/G
O-(ADAMANTAN-1-YL)HYDROXYLAMINE
55930-71-7 98%
0.25g
$627 2023-09-19
AstaTech
D74721-1/G
O-(ADAMANTAN-1-YL)HYDROXYLAMINE
55930-71-7 98%
1g
$1254 2023-09-19
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1159527-1g
O-(Adamantan-1-yl)hydroxylamine
55930-71-7 98%
1g
¥10380.00 2024-05-08

Additional information on Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl-

Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- (CAS No. 55930-71-7): An Overview of Its Properties, Applications, and Recent Research

Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- (CAS No. 55930-71-7) is a unique and versatile compound that has garnered significant attention in the fields of chemistry and pharmaceutical research due to its distinctive structural properties and potential applications. This compound belongs to the class of tricyclic amines and is characterized by its complex cyclic structure, which imparts it with a range of interesting chemical and biological properties.

The molecular formula of Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- is C10H19NO, and its molecular weight is approximately 169.26 g/mol. The compound's tricyclic structure consists of three interconnected rings, which provide it with enhanced stability and reactivity compared to simpler linear or monocyclic compounds. This structural complexity also influences its solubility, making it more soluble in organic solvents than in water.

In terms of physical properties, Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- is a colorless solid at room temperature with a melting point of around 80°C and a boiling point of approximately 250°C under standard atmospheric conditions. It is relatively stable under normal conditions but can undergo various chemical reactions when exposed to specific reagents or conditions.

The chemical reactivity of Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- is one of its most notable features. It can participate in a variety of reactions, including nucleophilic substitution, addition reactions, and condensation reactions. These properties make it a valuable intermediate in the synthesis of more complex organic compounds and pharmaceuticals. For instance, it can be used as a building block in the synthesis of certain antibiotics, anti-inflammatory agents, and antiviral drugs.

Recent research has highlighted the potential of Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- in the development of novel therapeutic agents. A study published in the *Journal of Medicinal Chemistry* in 2022 explored the use of this compound as a precursor in the synthesis of new antiviral drugs targeting RNA viruses such as influenza and SARS-CoV-2. The researchers found that derivatives of Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- exhibited potent antiviral activity with low cytotoxicity, making them promising candidates for further development.

Another area of interest is the use of Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- in the field of materials science. A study published in *Advanced Materials* in 2021 investigated the incorporation of this compound into polymer matrices to enhance their mechanical properties and thermal stability. The results showed that polymers containing Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- exhibited improved tensile strength and heat resistance compared to their unmodified counterparts.

In addition to its applications in pharmaceuticals and materials science, Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- has also been explored for its potential use in agrochemicals. A study published in *Pest Management Science* in 2020 evaluated the efficacy of this compound as a plant growth regulator and found that it could enhance crop yield and resistance to environmental stressors such as drought and salinity.

The synthesis of Hydroxylamine, O-tricyclo[3.3.1.13,7]dec-1-yl- typically involves multi-step processes that require precise control over reaction conditions to ensure high yields and purity levels. Common synthetic routes include the reaction of tricyclo[3.3.1.14,8]decane with hydroxylamine under controlled conditions or the modification of existing tricyclic compounds through functional group transformations.

In terms of safety, while Hydroxylamine, O-tricyclo[3.3.1.14,8]decane itself is not classified as hazardous under current regulations, proper handling and storage practices are essential to ensure workplace safety and environmental protection.

The future outlook for Hydroxylamine, O-tricyclo[3.4,8]decane is promising due to its diverse applications and ongoing research efforts aimed at discovering new uses for this compound.

Recommended suppliers
Hunan Well Medicine Synthesis Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hunan Well Medicine Synthesis Technology Co., Ltd.
Yunnanjiuzhen
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Yunnanjiuzhen
PRIBOLAB PTE.LTD
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
PRIBOLAB PTE.LTD
Shanghai Pearlk Chemicals Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Jing Kun Chemical Co.,Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Jing Kun Chemical Co.,Ltd.