40001-91-0

Basic information

• Product Name: 1,4,5,6-tetrachloro-7,7-dimethoxybicyclo[2.2.1]hept-5-en-2-yl acetate
• CAS NO: 40001-91-0
• Molecular Formula: C₁₁H₁₂Cl₄O₄
• Molecular Weight: 350.0226
• Mol File: 40001-91-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 354.2°C at 760 mmHg
• Flash Point: 131.8°C
• Density: 1.52g/cm³
• Vapor Pressure: 3.41E-05mmHg at 25°C
• Refractive Index: 1.549
• CAS DataBase Reference: 1,4,5,6-tetrachloro-7,7-dimethoxybicyclo[2.2.1]hept-5-en-2-yl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4,5,6-tetrachloro-7,7-dimethoxybicyclo[2.2.1]hept-5-en-2-yl acetate(40001-91-0)
• EPA Substance Registry System: 1,4,5,6-tetrachloro-7,7-dimethoxybicyclo[2.2.1]hept-5-en-2-yl acetate(40001-91-0)

Safety Data

• Hazardous Substances Data: 40001-91-0(Hazardous Substances Data)

Usage

Structure

Bicyclic compound with four chlorine atoms, two methoxy groups, and an acetate group attached to the carbon ring

Functional Groups

Chlorine atoms, methoxy groups, and an acetate group

Potential Applications

Industrial and research applications

Synthesis

Likely synthesized through organic synthesis methods, using the bicyclic compound as a starting material and introducing the chlorine, methoxy, and acetate groups

Physical Properties

Unknown, but may include appearance, density, melting point, and boiling point

Chemical Properties

Unknown, but may include reactivity, stability, and solubility

Hazards

Unknown, but may include toxicity, flammability, and environmental impact

Further Research

Additional research and testing needed to determine specific properties, applications, and potential hazards

Upstream product

• 108-05-4 vinyl acetate 
• 2207-27-4 5,5-dimethoxy-1,2,3,4-tetrachlorocyclopentadiene 

Downstream Products

• 10265-41-5 (1RS,2RS,4SR)-7,7-dimethoxybicyclo[2.2.1]heptan-2-ol 

Relevant articles and documents

Robust synthesis of enantiopure cyclohexenyl analogues of 2/3-deoxyribose sugars as carbocyclic nucleoside precursors

An expedient synthesis of 2-deoxy (10) and 3-deoxy (11) cyclohexenyl analogues of 2-deoxy and 3-deoxy-d-ribose sugar from commercially available starting materials is reported. Highly efficient enzymatic resolution of the key compound 10 is described usin

Synthetic studies related to CP-225,917

Synthetic studies related to CP-225,917 are described, including the preparation of the fully oxygenated tetracyclic central core 3.