850399-67-6

Basic information

• Product Name: 1,3-Benzenediol, 5-(phenylmethoxy)-, diacetate
• Synonyms: acetic acid 3-acetoxy-5-benzyloxy-phenyl ester
• CAS NO: 850399-67-6
• Molecular Formula: C17H16O5
• Molecular Weight: 300.311
• Mol File: 850399-67-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 440.8±40.0 °C(Predicted)
• Density: 1.204±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,3-Benzenediol, 5-(phenylmethoxy)-, diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Benzenediol, 5-(phenylmethoxy)-, diacetate(850399-67-6)
• EPA Substance Registry System: 1,3-Benzenediol, 5-(phenylmethoxy)-, diacetate(850399-67-6)

Safety Data

• Hazardous Substances Data: 850399-67-6(Hazardous Substances Data)

Usage

Derived from

Resorcinol (1,3-Benzenediol)

Phenylmethoxy

A phenyl group attached to a methoxy group

Acetate

Two acetyl groups attached to the molecule

Fragrance Industry

As a fixative

Synthesis

In the production of pharmaceuticals and agricultural products

Physical Appearance

White to off-white powder

Solubility

Soluble in organic solvents

Applications

Research and chemical manufacturing processes

Upstream product

• 2999-40-8 1,3,5-triacetoxybenzene 
• 100-44-7 benzyl chloride 
• 108-73-6 3,5-dihydroxyphenol 
• 116345-96-1 5-hydroxy-1,3-phenylene diacetate 
• 100-39-0 benzyl bromide 

Downstream Products

• 1412888-39-1 2,6-di-O-acetyl-4,4'-di-O-benzyl-benzophenone 
• 1412888-40-4 2,4-di-O-acetyl-4',6-di-O-benzyl-benzophenone 
• 1412888-35-7 2,4',6-O-trihydroxybenzophenone 4-O-β-D-galactopyranosyl-(1→4)-α-L-rhamnopyranoside 
• 1412888-34-6 2,4',6-O-trihydroxybenzophenone 4-O-β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranoside 
• 1412888-33-5 2,4',6-trihydroxybenzophenone 4-O-α-L-rhamnopyranoside 
• 1412888-32-4 4,4',6-O-trihydroxybenzophenone 2-O-α-L-rhamnopyranosyl-(1→4)-α-L-rhamnopyranoside 
• 1412888-68-6 2-O-benzyl-6-hydroxy-4'-O-benzyl-benzophenone 4-O-[2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl-(1→4)-α-L-rhamnopyranoside] 
• 1412888-67-5 2-O-benzyl-6-hydroxy-4'-O-benzyl-benzophenone 4-O-[2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1→4)-α-L-rhamnopyranoside] 
• 1412888-66-4 2-O-benzyl-6-hydroxy-4'-O-benzyl-benzophenone 4-O-[2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1→4)-α-L-rhamnopyranoside] 
• 1412888-65-3 2-O-benzyl-6-hydroxy-4'-O-benzyl-benzophenone 4-O-[2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1→4)-α-L-rhamnopyranoside] 
• 1412888-31-3 4,4',6-O-trihydroxybenzophenone 2-O-β-D-xylopyranosyl-(1→4)-α-L-rhamnopyranoside 
• 1412888-30-2 4,4',6-O-trihydroxybenzophenone 2-O-α-D-mannopyranosyl-(1→4)-α-L-rhamnopyranoside 
• 1412888-61-9 4'-O-benzyl-6-hydroxy-4-O-benzyl-benzophenone 2-O-[2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1→4)-α-L-rhamnopyranoside] 

Relevant articles and documents

Synthesis and evaluation of benzophenone O-glycosides as α-glucosidase inhibitors

The first total synthesis of benzophenone O-glycosides (iriflophenone 2-O-α-L-rhamnopyranoside: 1 and aquilarisinin: 2) isolated from the leaves of Aquilaria sinensis and related new derivatives (3-12) was accomplished through suitable protecting group ma

Dodecamethoxy- and hexaoxotricyclobutabenzene: Synthesis and characterization

We report herein the syntheses of dodecamethoxytricyclobutabenzene (TCBB) 1 and hexaoxo-TCBB 2, a class of molecules with structural and theoretical interest. The preparation is based on the 3-fold [2 + 2] cycloadditions of benzyne and ketene silyl acetal