4-Chloro-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Base Information

• Chemical Name: 4-Chloro-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
• CAS No.: 83697-03-4
• Molecular Formula: C₁₀H₁₇ClO
• Molecular Weight: 188.697
• NSC Number: 131297
• DSSTox Substance ID: DTXSID50299548

Synonyms:83697-03-4;4-Chloro-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol;NSC131297;DTXSID50299548;DUHPAWBYUJBSES-UHFFFAOYSA-N;NSC-131297;4-Chloro-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol #;Bicyclo[2.2.1]heptan-2-ol, 4-chloro-1,7,7-trimethyl-, exo-

Chemical Property of 4-Chloro-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Chemical Property:

• Vapor Pressure: 0.00547mmHg at 25°C
• Boiling Point: 243.3°Cat760mmHg
• Flash Point: 101°C
• Density: 1.12g/cm³
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 188.0967929
• Heavy Atom Count: 12
• Complexity: 226

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(C2(CCC1(CC2O)Cl)C)C

Technology Process of 4-Chloro-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

There total 7 articles about 4-Chloro-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

4-Chlor-isobornylformat → (+/-)-4-chloro-bornanol-(2exo) (34733-71-6,83697-03-4)

Guidance literature:

With potassium hydroxide; In methanol;

DOI:10.1021/jo00980a005

Reference yield:

(1R,4R)-1-chloro-3,3-dimethyl-2-methylenebicyclo[2.2.1]heptane (4017-64-5) → (+/-)-4-chloro-bornanol-(2exo) (34733-71-6,83697-03-4)

Guidance literature:

Multi-step reaction with 2 steps

2: aq. KOH / methanol

With potassium hydroxide; In methanol;

DOI:10.1021/jo00980a005

Reference yield:

→ (+)(1S)-4-chloro-bornanol-(2exo) (34733-71-6,83697-03-4)

Guidance literature:

With diethyl ether; oxygen;

upstream raw materials:

trichloroacetic acid

(1R,4R)-1-chloro-3,3-dimethyl-2-methylenebicyclo[2.2.1]heptane

Downstream raw materials:

isoborneol

(+/-)-4-chloro-camphor

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