Carthamidin

Base Information

• Chemical Name: Carthamidin
• CAS No.: 479-54-9
• Molecular Formula: C15H12 O6
• Molecular Weight: 288.257
• DSSTox Substance ID: DTXSID40963963
• Nikkaji Number: J1.761.577G
• Wikidata: Q27149852
• Mol file: 479-54-9.mol

Synonyms:(2S)-2,3-dihydro-5,6,7-trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;4',5,6,7-tetrahydroxy-flavanone;4',5,6,7-tetrahydroxyflavanone;5,6,7-trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;6-hydroxy-apigenin;6-hydroxyapigenin;6-hydroxynaringenin;carthamidin;scutellarein

Chemical Property of Carthamidin

Chemical Property:

• Vapor Pressure: 2.71E-18mmHg at 25°C
• Boiling Point: 665°Cat760mmHg
• PKA: 7.36±0.40(Predicted)
• Flash Point: 257.2°C
• PSA: 107.22000
• Density: 1.586g/cm³
• LogP: 2.21550
• XLogP3: 2
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 288.06338810
• Heavy Atom Count: 21
• Complexity: 392

Purity/Quality:

98.5% ^*data from raw suppliers

4',5,7,8-TETRAHYDROXYFLAVANONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC=C(C=C3)O
• Isomeric SMILES: C1[C@H](OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC=C(C=C3)O

Technology Process of Carthamidin

There total 6 articles about Carthamidin 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:

→ 5,6,7,4'-tetrahydroxyflavanone (479-54-9)

Guidance literature:

With aluminium trichloride; benzene;

Reference yield:

→ 5,6,7,4'-tetrahydroxyflavanone (479-54-9)

Guidance literature:

With phosphoric acid;

Reference yield:

→ 5,6,7,4'-tetrahydroxyflavanone (479-54-9)

Guidance literature:

With phosphoric acid;

upstream raw materials:

3-β-D-glucopyranosyloxy-5-hydroxy-2-(4-hydroxy-trans-cinnamoyl)-[1,4]benzoquinone

phosphoric acid

2'-β-D-glucopyranosyloxy-4,3',4',6'-tetrahydroxy-trans-chalcone

Downstream raw materials:

5,6,7-triacetoxy-2-(4-acetoxy-phenyl)-chroman-4-one