Phthalic acid hydrogen 1-[(1S)-1-methylheptyl] ester

Base Information

Chemical Name:Phthalic acid hydrogen 1-[(1S)-1-methylheptyl] ester
CAS No.:6114-64-3
Molecular Formula:C16H22O4
Molecular Weight:278.348
Hs Code.:2918990090
Mol file:6114-64-3.mol

Synonyms:(+)-Phthalic acid hydrogen 1-[(S)-1-methylheptyl] ester;Phthalic acid hydrogen 1-[(1S)-1-methylheptyl] ester

Suppliers and Price of Phthalic acid hydrogen 1-[(1S)-1-methylheptyl] ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of Phthalic acid hydrogen 1-[(1S)-1-methylheptyl] ester

Chemical Property:

PSA：63.60000
LogP:3.90050

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Phthalic acid hydrogen 1-[(1S)-1-methylheptyl] ester

There total 4 articles about Phthalic acid hydrogen 1-[(1S)-1-methylheptyl] ester 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: 49.0%

: 85-44-9
phthalic anhydride

: 108-05-4,9003-20-7
vinyl acetate

: 4128-31-8,113301-48-7,4128-32-9
rac-octan-2-ol

: 54712-18-4
(R)-2-octyl acetate

: 6114-64-3
2-{[(S)-octan-7-yloxy]carbonyl}benzoic acid

Guidance literature:: vinyl acetate; rac-octan-2-ol; In dichloromethane; at 20 ℃; for 16h; Inert atmosphere; Enzymatic reaction;

phthalic anhydride; With triethylamine; In dichloromethane; for 7h; optical yield given as %ee; enantioselective reaction; Reflux; Inert atmosphere;
DOI:10.1055/s-0029-1216997