(1S,2S,3R,4R)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester

Base Information

Chemical Name:(1S,2S,3R,4R)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester
CAS No.:132747-51-4
Molecular Formula:C₁₇H₁₈O₆
Molecular Weight:318.326
Hs Code.:

Synonyms:(1S,2S,3R,4R)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester

Suppliers and Price of (1S,2S,3R,4R)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> 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 0 raw suppliers

Chemical Property of (1S,2S,3R,4R)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1S,2S,3R,4R)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester

There total 6 articles about (1S,2S,3R,4R)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> 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: 66.0%

: 131466-58-5,132674-12-5,132747-50-3
(1S,2R,3S,4R)-Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid mono-[(4-methoxy-benzyloxycarbonyl)-phenyl-methyl] ester

: 129910-29-8
(1R,2R,3S,4S)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester

: 132747-51-4
(1S,2S,3R,4R)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester

Guidance literature:: With hydrogenchloride; In acetonitrile; Yields of byproduct given;
DOI:10.1021/jo00006a030

Reference yield: 66.0%

: 131466-57-4,132747-49-0,135029-22-0
(1S,2R,3S,4R)-Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid mono-(benzhydryloxycarbonyl-phenyl-methyl) ester

: 129910-29-8
(1R,2R,3S,4S)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester

: 132747-51-4
(1S,2S,3R,4R)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester

Guidance literature:: With hydrogenchloride; In acetonitrile; Yields of byproduct given;
DOI:10.1021/jo00006a030

Reference yield: 65.0%

: 129910-28-7,131564-23-3
(1S,2R,3S,4R)-Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid mono-(benzyloxycarbonyl-phenyl-methyl) ester

: 129910-29-8
(1R,2R,3S,4S)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester

: 132747-51-4
(1S,2S,3R,4R)-Bicyclo<2.2.1>heptane-2,3-dicarboxylic Acid 2-<(R)-Mandelic acid> Ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 1.5h; under 760 Torr; Yields of byproduct given; Ambient temperature;
DOI:10.1021/jo00006a030