Pseudopurpurin

Base Information

• Chemical Name: Pseudopurpurin
• CAS No.: 476-41-5
• Molecular Formula: C15H8O7
• Molecular Weight: 300.224
• DSSTox Substance ID: DTXSID30197210
• Nikkaji Number: J12.549K
• Wikidata: Q27108112
• Metabolomics Workbench ID: 69448
• Mol file: 476-41-5.mol

Synonyms:Pseudopurpurin;Pseudopurpurine;476-41-5;2-Anthracenecarboxylic acid, 9,10-dihydro-1,3,4-trihydroxy-9,10-dioxo-;C10394;AC1L9DDH;CTK1D7829;CHEBI:8608;SCHEMBL5075855;1,3,4-trihydroxy-9,10-dioxo-anthracene-2-carboxylic acid;C15H8O7;DTXSID30197210;Q27108112

Chemical Property of Pseudopurpurin

Chemical Property:

• Vapor Pressure: 2.87E-13mmHg at 25°C
• Boiling Point: 557.6°Cat760mmHg
• Flash Point: 305.1°C
• Density: 1.798g/cm³
• XLogP3: 3
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 1
• Exact Mass: 300.02700259
• Heavy Atom Count: 22
• Complexity: 516

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C(=C3O)C(=O)O)O)O
• Use Description: 2-Anthracenecarboxylic acid, 9,10-dihydro-1,3,4-trihydroxy-9,10-dioxo-, is a chemical compound with applications in various fields. In the field of organic chemistry and pharmaceuticals, it can serve as a key intermediate for the synthesis of specialized organic molecules, potentially contributing to the development of pharmaceutical drugs and bioactive compounds due to its versatile structure. In the realm of research and analytical chemistry, this compound may find use as a reference material or standard for the characterization and quantification of related chemicals, aiding in chemical analysis and research. Additionally, in the dye and pigment industry, it can be employed as a precursor for the synthesis of anthraquinone-based dyes and pigments, contributing to the coloration of various products, including textiles and inks. Its adaptability as an intermediate, reference compound, and dye precursor underscores its significance in advancing pharmaceuticals, chemical analysis, and coloration technology in various fields.

Technology Process of Pseudopurpurin

There total 8 articles about Pseudopurpurin 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:

1,2,4-trihydroxy-9,10-anthraquinone (81-54-9) → pseudopurpurin (476-41-5)

Guidance literature:

With sodium hydroxide; formaldehyd; at 70 ℃; Erhitzen des Reaktionsprodukts mit Natriumnitrit, Borsaeure und Schwefelsaeure auf 145grad;

DOI:10.1007/BF02886201

Reference yield:

1,4-dihydroxy-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid (6416-55-3) → pseudopurpurin (476-41-5)

Guidance literature:

With manganese(IV) oxide; sulfuric acid; Behandlung des Reaktionsproduktes mit verd. NaHSO₃-Loesung;

Reference yield:

3,4-dihydroxy-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid (6373-38-2) → pseudopurpurin (476-41-5)

Guidance literature:

With manganese(IV) oxide; sulfuric acid; Behandlung des Reaktionsproduktes mit verd. NaHSO₃-Loesung;

upstream raw materials:

1,2,4-trihydroxy-9,10-anthraquinone

2-methylanthracene-9,10-dione

1,4-dihydroxy-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid

3,4-dihydroxy-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid

Downstream raw materials:

1,2,4-trihydroxy-9,10-anthraquinone

carbon dioxide

1,3-dihydroxy-9,10-anthraquinone-2-carboxylic acid

1-amino-2,4-dihydroxy-anthraquinone