21782-87-6

Basic information

• Product Name: Benzoic acid,2,5-dihydroxy-,phenylmethyl ester
• CAS NO: 21782-87-6
• Molecular Weight: 244.247
• Mol File: 21782-87-6.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzoic acid,2,5-dihydroxy-,phenylmethyl ester (CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid,2,5-dihydroxy-,phenylmethyl ester (21782-87-6)
• EPA Substance Registry System: Benzoic acid,2,5-dihydroxy-,phenylmethyl ester (21782-87-6)

Safety Data

• Hazardous Substances Data: 21782-87-6(Hazardous Substances Data)

Upstream product

• 490-79-9 2,5-dihydroxybenzoic acid. 
• 100-39-0 benzyl bromide 
• 108-88-3 toluene 
• 100-44-7 benzyl chloride 
• 4955-90-2 sodium 2,5-dihydroxybenzoate 
• 10590-85-9 benzyl 2-(β-D-glucopyranosyloxy)-5-hydroxybenzoate 

Downstream Products

• 490-79-9 2,5-dihydroxybenzoic acid. 
• 433287-50-4 2-benzyloxycarbonyl-1,4-benzoquinone 
• 205689-93-6 2,5-di(4'-butyloxybenzoyloxy)benzoic acid 
• 1429519-53-8 C₃₂H₃₄O₈ 
• 131355-99-2 (but-3''-enyl) 2,5-di(4'-butyloxybenzoyloxy)benzoate 
• 210816-66-3 C₃₅H₄₀O₈ 
• 205689-89-0 benzyl 2,5-di(4'-butyloxybenzoyloxy)benzoate 
• 20633-70-9 trichocarpine tetraacetate 
• 17019-77-1 benzyl 2-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-5-acetoxybenzoate 
• 433287-48-0 2-amino-5-(4-N-benzylamino-5-carboxybenzyl-3,6-dioxocyclohexa-1,4-dienyl)-6-hydroxy-3-methoxybenzoic acid 
• 433287-47-9 3-benzylamino-2-benzyloxycarbonyl-1,4-benzoquinone 

Relevant articles and documents

PHENOLIC GLYCOSIDES FROM SALIX BABYLONICA

Key Word Index - Salix babylonica; Salicaceae; 2'-O-acetyltrichocarpin; trichocarpin; salicin; flavonoid glucosides, Abstract - From the leaves of Salix babylonica, the new naturally occurring benzyl ester of gentisic acid 2'-O-acetyl β-D-glucoside has be

MONOMER, POLYMER, COMPENSATION FILM, OPTICAL FILM, AND DISPLAY DEVICE

A monomer is represented by Chemical Formula 1: wherein, in Chemical Formula 1, R1, R2, o, p, L1, A1, Ra, m, and n are the same as defined in the detailed description.

Catalytic asymmetric synthesis of aryl diphenol the axis chiral is joint method

The invention discloses a method for catalyzing asymmetrically synthesized axially chiral biaryl diphenol. In an organic solvent, chiral phosphoric acid is taken as a catalyst, a compound shown in a formula III is obtained by reaction on a compound shown