252044-63-6

Basic information

• Product Name: O^α-(tetrahydropyran-2-yl)-L-mandelic acid
• Synonyms: O^α-(tetrahydropyran-2-yl)-L-mandelic acid
• CAS NO: 252044-63-6
• Molecular Weight: 236.268
• Mol File: 252044-63-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: O^α-(tetrahydropyran-2-yl)-L-mandelic acid(CAS DataBase Reference)
• NIST Chemistry Reference: O^α-(tetrahydropyran-2-yl)-L-mandelic acid(252044-63-6)
• EPA Substance Registry System: O^α-(tetrahydropyran-2-yl)-L-mandelic acid(252044-63-6)

Safety Data

• Hazardous Substances Data: 252044-63-6(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 17199-29-0 (S)-Mandelic acid 
• 21210-43-5 (S)-Methyl mandelate 
• 155486-11-6 (S)-Phenyl-[(tetrahydro-pyran-2-yloxy)]-acetic acid methyl ester 

Downstream Products

• 497107-20-7 5-bromo-1,3-bis[(4S)-4-hydroxy-4-phenyl-2-oxobutyl]-2-methoxybenzene 
• 252044-69-2 O^α-(9-fluorenylmethyloxycarbonyl)-L-mandeloyl-L-mandeloyl-L-mandelic acid methyl ester 
• 252044-73-8 O^α-(tetrahydropyran-2-yl)-L-mandeloyl-L-mandeloyl-L-mandelic acid methyl ester 
• 252044-72-7 L-mandeloyl-L-mandeloyl-L-mandelic acid methyl ester 
• 252044-71-6 L-mandeloyl-D-mandeloyl-L-mandelic acid methyl ester 
• 252044-67-0 L-mandeloyl-L-mandelic acid methyl ester 
• 220728-58-5 H-[L-Man]6-OH 
• 252044-68-1 O^α-(tetrahydropyran-2-yl)-L-mandeloyl-L-mandelic acid methyl ester 
• 1027401-37-1 C₂₀H₂₆O₇ 

Relevant articles and documents

Solid phase synthesis of depsides and depsipeptides

A general solid phase methodology for the synthesis of depside and depsipeptide chains from optically active α-hydroxy acids and α-amino acids is reported. The automated preparation of depsides (97% yield per cycle) made up from the same enantiomer (i.e.

A general methodology for automated solid-phase synthesis of depsides and depsipeptides. Preparation of a valinomycin analogue

A general methodology is described that allows the solid-phase synthesis of depsides and depsipeptides from chiral α-hydroxy- and α-amino acids. The results of studies with different protecting groups for the α-hydroxy acids and coupling systems for depsi