Cas no 13851-11-1 (Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate)

Technical Introduction: Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate is a bicyclic terpene derivative characterized by its rigid molecular structure and functional acetate group. This compound exhibits notable stability due to its fused ring system, making it suitable for applications requiring robust chemical frameworks. The presence of the acetate moiety enhances its solubility in organic solvents, facilitating its use in synthetic chemistry and fragrance formulations. Its stereochemistry and steric hindrance contribute to selective reactivity, advantageous for chiral synthesis or as an intermediate in fine chemical production. The compound's structural features also lend potential utility in polymer modification or as a precursor for specialized derivatives.
Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate structure
13851-11-1 structure
Product Name:Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate
CAS No:13851-11-1
MF:C12H20O2
MW:196.286004066467
CID:141677
Update Time:2025-10-17

Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate Chemical and Physical Properties

Names and Identifiers

    • Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate
    • ALPHA FENCHYL ACETATE
    • 1,3,3-TRIMETHYL-2-NORBONYLACETATE
    • 1,3,3-trimethyl-2-norbornanoacetate
    • 1,3,3-TRIMETHYL-2-NORBORNANYL ACETATE
    • 2-Norbornanol,1,3,3-trimethyl-,acetate
    • 3,3-dimethyl-8,9-dinorbornan-2-yl acetate
    • Essigsaeure-fenchylester
    • FEMA 3390
    • FENCHYLACETAT MIN. 95 P.
    • Fenchylacetate
    • 1,3,3-trimethyl-bicyclo(2.2.1)heptan-2-o acetate
    • 1,3,3-trimethyl-bicyclo[2.2.1]heptan-2-o acetate
    • Fenchyl acetate (Isomer)
    • (1R)-(+)-FENCHYL ACETATE
    • 1,3,3-trimethyl-2-norbornano acetate
    • FENCHYL ACETATE
    • FENCHYL ACETATE 90%
    • Inchi： 1S/C12H20O2/c1-8(13)14-10-11(2,3)9-5-6-12(10,4)7-9/h9-10H,5-7H2,1-4H3/t9-,10?,12+/m1/s1
    • InChI Key： JUWUWIGZUVEFQB-MAZPRZIYSA-N
    • SMILES： [C@@]12(C)CC[C@@]([H])(C(C)(C)C1OC(=O)C)C2

Computed Properties

  • Exact Mass: 196.14600

Experimental Properties

  • Density: 0.98?g/mL?at 25?°C(lit.)
  • Boiling Point: 220?°C(lit.)
  • Flash Point: 168?°F
  • Refractive Index: n20/D 1.456(lit.)
  • PSA: 26.30000
  • LogP: 2.76430
  • FEMA: 3390 | 1,3,3-TRIMETHYL-2-NORBORNANYL ACETATE

Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate Security Information

  • WGK Germany：2
  • Hazard Category Code： 36/37/38
  • Safety Instruction： S26; S36
  • RTECS：RB7660000
  • Hazardous Material Identification： Xi
  • Risk Phrases：R36/37/38

Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate Customs Data

  • HS CODE：2915390090
  • Customs Data：

    China Customs Code:

    2915390090

    Overview:

    2915390090. Other acetate esters. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:AB(Customs clearance form for Inbound Goods,Customs clearance form for outbound goods). MFN tariff:5.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Regulatory conditions:

    A.Customs clearance form for Inbound Goods
    B.Customs clearance form for outbound goods

    Inspection and quarantine category:

    R.Sanitary supervision and inspection of imported food
    S.Sanitary supervision and inspection of exported food
    M.Import commodity inspection
    N.Export commodity inspection

    Summary:

    2915390090. esters of acetic acid. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:5.5%. General tariff:30.0%

Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd.
W339008-SAMPLE
Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate
 13851-11-1 ≥96%, FG
587.6 2021-05-17
XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd.
W339008-1KG
Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate
 13851-11-1
1kg
 ￥1687.97 2023-11-12
XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd.
W339008-5KG
Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate
 13851-11-1
5kg
 ￥6873.8 2023-11-12
XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd.
W339008-10KG
Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate
 13851-11-1
10kg
 ￥12691.54 2023-11-12
TargetMol Chemicals
T31767-25mg
Fenchyl acetate
 13851-11-1
25mg
 ￥ 10600 2024-07-20
TargetMol Chemicals
T31767-5 mg
Fenchyl acetate
 13851-11-1 98%
5mg
 ￥ 7,000 2023-07-11
TargetMol Chemicals
T31767-5mg
Fenchyl acetate
 13851-11-1 98%
5mg
 ￥ 7000 2023-09-15

Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate Related Literature

Related Categories

Additional information on Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate

Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate (CAS No. 13851-11-1)

Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, 2-acetate (commonly referred to as Bicyclo[2.2.1]heptan-2-ol) is a bicyclic compound with a unique structural configuration that has garnered significant attention in the fields of organic chemistry and materials science. This compound is characterized by its bicyclo[2.2.1]heptane framework, which consists of two fused six-membered rings and a five-membered ring, creating a highly rigid and stable molecular structure.

The bicyclo[2.2.1]heptane system is notable for its resistance to conformational changes due to the strain inherent in its structure. This property makes it an ideal candidate for applications requiring high thermal stability and mechanical robustness. Recent studies have highlighted its potential in the development of advanced polymers and high-performance materials.

Bicyclo[2.2.1]heptan-2-ol is often synthesized through a combination of Diels-Alder reactions and subsequent functionalization steps. The synthesis process involves the formation of the bicyclic core followed by the introduction of hydroxyl and acetate groups at specific positions on the molecule.

The compound's bicyclo[2.2.1]heptane framework also plays a crucial role in its optical properties. Research has shown that this structure can exhibit strong fluorescence under certain conditions, making it a promising candidate for applications in optoelectronics and sensing technologies.

In terms of chemical reactivity, Bicyclo[2.2.1]heptan-2-ol demonstrates selective reactivity towards nucleophilic substitution reactions due to the electron-withdrawing effects of the acetate group at position 2 of the molecule.

Recent advancements in computational chemistry have enabled detailed studies of the electronic structure of Bicyclo[2.2.1]heptan-2-ol, providing insights into its reactivity and potential for use in catalytic processes.

The compound's bicyclo[...] framework has also been explored in drug design applications due to its ability to mimic natural product structures while maintaining synthetic accessibility.

Furthermore, Bicyclo[...] systems are being investigated for their potential in creating novel materials with tailored mechanical properties for use in aerospace and automotive industries.

As research continues to uncover new applications for Bicyclo[...] compounds, their role in modern chemistry is expected to grow significantly over the coming years.

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