2,3,5,6,8-Pentahydroxy-1,4-naphthoquinone

Base Information

Chemical Name:2,3,5,6,8-Pentahydroxy-1,4-naphthoquinone
CAS No.:1143-11-9
Molecular Formula:C10H6 O7
Molecular Weight:238.153
Hs Code.:2914690090
Mol file:1143-11-9.mol

Synonyms:1,4-Naphthoquinone,2,3,5,6,8-pentahydroxy- (7CI,8CI); 2,3,5,6,8-Pentahydroxy-1,4-naphthoquinone;Spinochrom D; Spinochrome D

Suppliers and Price of 2,3,5,6,8-Pentahydroxy-1,4-naphthoquinone

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
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price

Total 6 raw suppliers

Chemical Property of 2,3,5,6,8-Pentahydroxy-1,4-naphthoquinone

Chemical Property:

PSA：135.29000
LogP:0.51000

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

General Description 2,3,5,6,8-Pentahydroxy-1,4-naphthoquinone, also known as Spinochrome D, is a naturally occurring metabolite found in sea urchins. It can be synthesized through oxidative and nucleophilic substitution reactions, such as the oxidation of 2,3-dichloronaphthazarin followed by O-methylation and hydrolysis, or via acid-catalyzed condensation of substituted 2-hydroxy-1,4-naphthoquinones with alcohols. These methods provide efficient pathways for its preparation, highlighting its significance as a bioactive quinone derivative.

Technology Process of 2,3,5,6,8-Pentahydroxy-1,4-naphthoquinone

There total 22 articles about 2,3,5,6,8-Pentahydroxy-1,4-naphthoquinone 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: 92.0%