Description

Bicyclo2.2.1Heptan-2-Ol, 4,7,7-Trimethyl-3-(Phenylmethoxy)-, Formate, 1S-(Exo,Exo)- is a high-purity, specialized organic compound belonging to the class of functionalized bicyclic terpenoids. This chemical serves as a valuable chiral building block and advanced intermediate for the synthesis of complex molecules, offering precise stereochemical control. It is primarily sought after by research institutions and industrial R&D teams in the pharmaceutical and fine chemical sectors for developing novel active ingredients and fragrances.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the research and development of new active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring complex molecular architectures.
• Asymmetric Synthesis: Utilized as a precursor or ligand in catalytic asymmetric reactions to induce high enantioselectivity in target compounds.
• Fragrance & Flavor Chemistry: Serves as a building block for synthesizing novel odorants and flavor molecules with unique olfactory profiles derived from its modified camphor-like structure.
• Agrochemical Research: Employed in the development of new, more selective pesticides and herbicides where specific stereochemistry is crucial for bioactivity.
• Material Science: Investigated as a monomer or functional additive for creating polymers with specific thermal or optical properties.
• Academic & Industrial R&D: Used in methodological studies and process chemistry development as a model substrate for new synthetic transformations.

Basic Information

Product Name	Bicyclo2.2.1Heptan-2-Ol, 4,7,7-Trimethyl-3-(Phenylmethoxy)-, Formate, 1S-(Exo,Exo)-
CAS No.	110259-75-1
Molecular Formula	C18H24O3
Molecular Weight	288.38 g/mol
Synonyms	1S-(exo,exo)-3-(Benzyloxy)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate; 3-(Benzyloxy)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol formate (1S-exo,exo); exo-3-(Benzyloxy)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate; (1S,2R,3S,4R)-3-(Benzyloxy)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl formate; Functionalized Camphor Derivative; Bicyclo[2.2.1]heptane-2-ol, 3-(phenylmethoxy)-, 1,7,7-trimethyl-, formate, (1S-endo)-; Contact for additional synonyms.
EINECS	Contact for details

Quality Control

Our production of Bicyclo2.2.1Heptan-2-Ol, 4,7,7-Trimethyl-3-(Phenylmethoxy)-, Formate, 1S-(Exo,Exo)- adheres to stringent internal quality standards to ensure batch-to-batch consistency and high chemical purity. Each lot is characterized using advanced analytical techniques including HPLC, GC, NMR, and chiral analysis to confirm identity, purity, and stereochemical integrity. A comprehensive Certificate of Analysis (COA) detailing all test results is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep away from heat, sparks, and open flame. For long-term storage, consider maintaining the material under an inert atmosphere to preserve stability.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid or low-melting solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC/GC)	≥ 97.0%
Chiral Purity (Chiral HPLC/GC)	≥ 98.0% ee (1S-exo,exo)
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.