endo-1,7,7-Trimethylbicyclo(2.2.1)-2-heptanol, 97%

Base Information

• Chemical Name: endo-1,7,7-Trimethylbicyclo(2.2.1)-2-heptanol, 97%
• CAS No.: 13429-57-7
• Molecular Formula: C10H18 O
• Molecular Weight: 154.252
• Hs Code.: 2906199090
• Mol file: 13429-57-7.mol

Synonyms:2-Norbornanol,2,3,3-trimethyl-, stereoisomer (8CI); Bicyclo[2.2.1]heptan-2-ol,2,3,3-trimethyl-, endo- (9CI); 2b,3,3-Trimethylnorbornan-2a-ol

Chemical Property of endo-1,7,7-Trimethylbicyclo(2.2.1)-2-heptanol, 97%

Chemical Property:

• PSA: 20.23000
• LogP: 2.19350

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of endo-1,7,7-Trimethylbicyclo(2.2.1)-2-heptanol, 97%

There total 14 articles about endo-1,7,7-Trimethylbicyclo(2.2.1)-2-heptanol, 97% 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:

diethyl ether (60-29-7,927820-24-4) + N-(R)-(+)-bornylamine (37606-04-5) + water (7732-18-5) → camphene (5794-04-7) + (-)-(S)-α-terpineol (10482-56-1,2438-12-2) + (+)-camphene hydrate (465-31-6,13429-40-8,13429-57-7,28974-22-3,52437-40-8,64397-62-2,64474-11-9,91547-95-4)

Guidance literature:

das Hydrogensulfat reagiert;

Reference yield:

bornyl chloride (464-41-5,559-45-5,6120-13-4,27720-69-0,30462-53-4,33602-15-2,73804-39-4,91547-96-5) → camphene hydrate (13429-40-8,13429-57-7,52437-40-8,64397-62-2,64474-11-9,91547-95-4,465-31-6,28974-22-3) + rac-endo-borneol (6627-72-1) + dl-camphene (565-00-4) + 1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol (507-70-0)

Guidance literature:

at 130 - 150 ℃;

Reference yield:

4-chloro-2-isopropyl-5-methyl-benzenesulfonic acid isobornyl ester + furan-2,3,5(4H)-trione pyridine (1:1) → camphene hydrate (13429-40-8,13429-57-7,52437-40-8,64397-62-2,64474-11-9,91547-95-4,465-31-6,28974-22-3) + dl-camphene (565-00-4) + 1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol (507-70-0)

Guidance literature:

at 50 ℃;

upstream raw materials:

bornyl chloride

bornan-exo-2-yl bromide

4-chloro-2-isopropyl-5-methyl-benzenesulfonic acid bornyl ester

glycerol

Downstream raw materials:

camphene

isobornyl acetate

dl-camphene

Camphor

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