Cyclohexanecarboxylic acid, 3,4-dihydroxy-, (1R,3R,4R)-rel-

Base Information Edit

Chemical Name:Cyclohexanecarboxylic acid, 3,4-dihydroxy-, (1R,3R,4R)-rel-
CAS No.:23477-88-5
Molecular Formula:C₇H₁₂O₄
Molecular Weight:160.17
Hs Code.:
Mol file:23477-88-5.mol

Synonyms:

Suppliers and Price of Cyclohexanecarboxylic acid, 3,4-dihydroxy-, (1R,3R,4R)-rel-

Supply Marketing:Edit

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 13 raw suppliers

Chemical Property of Cyclohexanecarboxylic acid, 3,4-dihydroxy-, (1R,3R,4R)-rel- Edit

Chemical Property:

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Use Description Cyclohexanecarboxylic acid, 3,4-dihydroxy-, (1R,3R,4R)-rel-, also known as D-threo-3,4-dihydroxyphenylserine or DOPS, is a chemical compound with multifaceted applications in various fields. In the pharmaceutical and medical sectors, DOPS is primarily employed as a therapeutic agent for treating rare neurological disorders, such as Parkinson's disease and certain forms of autonomic dysfunction. It acts as a precursor for dopamine, a neurotransmitter crucial for motor function and mood regulation. In the field of neurochemistry and neuroscience research, DOPS is used to study neurotransmitter systems and their role in neurological diseases. Additionally, it has potential applications in the development of drug delivery systems and as a chiral building block in organic synthesis. DOPS plays a vital role in enhancing the quality of life for patients with specific medical conditions, advancing our understanding of neurobiology, and contributing to the synthesis of novel compounds with pharmaceutical and chemical significance.

Technology Process of Cyclohexanecarboxylic acid, 3,4-dihydroxy-, (1R,3R,4R)-rel-

There total 6 articles about Cyclohexanecarboxylic acid, 3,4-dihydroxy-, (1R,3R,4R)-rel- 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:

: 88255-83-8,116498-92-1,126873-60-7
3,4-Dihydroxycyclohexanecarboxylic acid-γ-lactone

: 23477-88-5,31540-11-1,32746-99-9,50426-47-6,67068-73-9,67068-74-0,76704-84-2,333364-12-8
(+/-)-(1R*,3R*,4R*)-3,4-dihydroxycyclohexanecarboxylic acid

Guidance literature:: With potassium hydroxide; water; In tetrahydrofuran;

Reference yield:

: 4771-80-6
1,2,5,6-tetrahydrobenzoic acid

: 23477-88-5,31540-11-1,32746-99-9,50426-47-6,67068-73-9,67068-74-0,76704-84-2,333364-12-8
(+/-)-(1R*,3R*,4R*)-3,4-dihydroxycyclohexanecarboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: 3-chloro-benzenecarboperoxoic acid / tetrachloromethane / 4 h

1.2: 4 h / 65 °C

2.1: water; potassium hydroxide / tetrahydrofuran

With water; 3-chloro-benzenecarboperoxoic acid; potassium hydroxide; In tetrahydrofuran; tetrachloromethane;