365534-57-2

Basic information

• Product Name: 2-(hydroxymethyl)benzoic acid benzyl ester
• Synonyms: 2-(hydroxymethyl)benzoic acid benzyl ester
• CAS NO: 365534-57-2
• Molecular Weight: 242.274
• Mol File: 365534-57-2.mol

Chemical Properties

• CAS DataBase Reference: 2-(hydroxymethyl)benzoic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(hydroxymethyl)benzoic acid benzyl ester(365534-57-2)
• EPA Substance Registry System: 2-(hydroxymethyl)benzoic acid benzyl ester(365534-57-2)

Safety Data

• Hazardous Substances Data: 365534-57-2(Hazardous Substances Data)

Upstream product

• 87-41-2 2-benzofuran-1(3H)-one 
• 100-39-0 benzyl bromide 

Downstream Products

• 532959-21-0 2-((2S,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxymethyl)-benzoic acid benzyl ester 
• 113674-51-4 2-Carbobenzoxybenzaldehyde 
• 365535-64-4 2-(benzyloxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranoside 
• 365535-62-2 2-(benzyloxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 365535-55-3 2'-(benzyloxycarbonyl)benzyl β-D-glucopyranoside 
• 365534-66-3 2-(hydroxycarbonyl)benzyl 4,6-O-benzoyl-2,3-O-cyclohexylidene-α-D-mannopyranoside 
• 365534-61-8 2-(benzyloxycarbonyl)benzyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 365534-65-2 2-(hydroxycarbonyl)benzyl 2,3-di-O-benzyl-4,6-O-cyclohexylidene-α-D-mannopyranoside 
• 365534-69-6 2-(hydroxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranoside 
• 365534-68-5 2-(hydroxycarbonyl)benzyl 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 365534-63-0 2-(hydroxycarbonyl)benzyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 365535-43-9 2'-(benzyloxycarbonyl)benzyl 4,6-O-benzylidene-α-D-mannopyranoside 
• 365535-50-8 2-(benzyloxycarbonyl)benzyl 4,6-di-O-benzoyl-2,3-O-cyclohexylidene-α-D-mannopyranoside 
• 365535-46-2 2-(benzyloxycarbonyl)benzyl 2,3-di-O-benzyl-4,6-O-cyclohexylidene-α-D-mannopyranoside 

Relevant articles and documents

Asymmetric Dieckmann Condensation towards Spirocyclic Oxindoles Catalyzed by Amino Acid-Derived Phosphonium Salts

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2-(Benzyloxycarbonyl)benzyl (BCB) glycosides were prepared by coupling of the corresponding tetraacetylglycosyl bromides and benzyl 2-(hydroxymethyl)benzoate. The BCB glycosides were converted almost quantitatively into the corresponding 2-(hydroxycarbony

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