51033-46-6

Basic information

• Product Name: 2,10-dihydroxy-5-(4-hydroxy-2-methoxyphenyl)-6-[(4-hydroxy-3-methoxyphenyl)methyl]-1,3-dimethoxy-9H-benzo[a]xanthen-9-one
• Synonyms: 2,10-dihydroxy-5-(4-hydroxy-2-methoxyphenyl)-6-[(4-hydroxy-3-methoxyphenyl)methyl]-1,3-dimethoxy-9H-benzo[a]xanthen-9-one;Santalin B;6-(4-Hydroxy-3-methoxybenzyl)-2,10-dihydroxy-5-(4-hydroxy-2-methoxyphenyl)-1,3-dimethoxy-9H-benzo[a]xanthene-9-one;Santalin A 3''-methyl ether;2,10-dihydroxy-5-(4-hydroxy-2-methoxyphenyl)-6-[(4-hydroxy-3-methoxyphenyl)methyl]-1,3-dimethoxy-9H-benzo[a]xanthen-9-one
• CAS NO: 51033-46-6
• Molecular Formula: C₃₄H₂₈O₁₀
• Molecular Weight: 596.58012
• EINECS: 256-926-2
• Mol File: 51033-46-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 1022.5°Cat760mmHg
• Flash Point: 334.1°C
• Appearance: /
• Density: 1.52g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.735
• CAS DataBase Reference: 2,10-dihydroxy-5-(4-hydroxy-2-methoxyphenyl)-6-[(4-hydroxy-3-methoxyphenyl)methyl]-1,3-dimethoxy-9H-benzo[a]xanthen-9-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2,10-dihydroxy-5-(4-hydroxy-2-methoxyphenyl)-6-[(4-hydroxy-3-methoxyphenyl)methyl]-1,3-dimethoxy-9H-benzo[a]xanthen-9-one(51033-46-6)
• EPA Substance Registry System: 2,10-dihydroxy-5-(4-hydroxy-2-methoxyphenyl)-6-[(4-hydroxy-3-methoxyphenyl)methyl]-1,3-dimethoxy-9H-benzo[a]xanthen-9-one(51033-46-6)

Safety Data

• Hazardous Substances Data: 51033-46-6(Hazardous Substances Data)

Usage

Molecular structure

The compound has a complex molecular structure, which includes multiple hydroxyl and methoxy groups attached to phenyl and xanthene moieties.

Type of compound

It is a chemical compound, specifically a derivative of benzo[a]xanthene, which is a tricyclic aromatic hydrocarbon.

Hydroxyl groups

The molecule contains several hydroxyl (-OH) groups, which contribute to its antioxidant properties and potential therapeutic applications.

Methoxy groups

The presence of methoxy (-OCH3) groups in the molecule also plays a role in its chemical properties and potential applications.

Xanthene ring

The compound contains a xanthene ring, which is a key structural feature of this class of compounds.

Antioxidant properties

Due to the presence of multiple hydroxyl groups, the compound exhibits potent antioxidant properties.

Therapeutic potential

The compound has potential therapeutic applications, as it may offer benefits in the fields of medicine and material science.

Interesting target for study

The intricate structure and functional groups present in this chemical make it an interesting target for further research and exploration in various fields.

InChI:InChI=1/C34H28O10/c1-40-27-13-18(35)6-7-19(27)30-20-14-29(42-3)32(39)34(43-4)31(20)22-11-17-12-24(37)25(38)15-26(17)44-33(22)21(30)9-16-5-8-23(36)28(10-16)41-2/h5-8,10-15,35-38H,9H2,1-4H3

Upstream product

• 97-53-0 4-allylguaiacol 
• 91-10-1 1,3-dimethoxy-2-hydroxy-benzene 
• 18111-34-7 3-bromo-2,6-dimethoxyphenol 

Relevant articles and documents

Biomimetic synthesis of santalin a,b and santarubin a,b, the major colorants of red sandalwood

Better late than never! Almost 200 years after Pelletier's pioneering studies on the chemical constituents of red sandalwood, the major santalins and santarubins have been synthesized. This efficient approach integrates a Knochel isoflavonoid synthesis with Friedel-Crafts allylations or olefin metatheses, and a final biomimetic reaction cascade that furnishes the venerable benzoxanthenone dyes in a single operation (see scheme). Copyright