127102-27-6

Basic information

• Product Name: benzyl L-threo-1,3-dihydroxy-1-phenylpropan-2-yl-carbamate
• Synonyms: benzyl L-threo-1,3-dihydroxy-1-phenylpropan-2-yl-carbamate
• CAS NO: 127102-27-6
• Molecular Weight: 301.342
• Mol File: 127102-27-6.mol

Chemical Properties

• CAS DataBase Reference: benzyl L-threo-1,3-dihydroxy-1-phenylpropan-2-yl-carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl L-threo-1,3-dihydroxy-1-phenylpropan-2-yl-carbamate(127102-27-6)
• EPA Substance Registry System: benzyl L-threo-1,3-dihydroxy-1-phenylpropan-2-yl-carbamate(127102-27-6)

Safety Data

• Hazardous Substances Data: 127102-27-6(Hazardous Substances Data)

Upstream product

• 28143-91-1 (1S,2S)-2-amino-1-phenyl-1,3-diol 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 175415-16-4 (1S,2S)-2-benzyloxycarbonylamino-1-phenyl-1,3-propanediol-3-methanesulfonyl ester 
• 127086-83-3 (1S,2S)-2-(N-carbobenzyloxy-N-methylamino)-3-phenyl-3-hydroxy-1-(tert-butyldimethylsilyl)propanol 
• 127086-90-2 2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4-<2-<<(p-nitrophenyl)sulfonyl>oxy>ethyl>phenoxy>ethyl>-4-benzyl-5-<(tert-butylcarboxy)amino>oxazole 
• 127086-87-7 2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4-<(isopropoxycarbonyl)methyl>phenoxy>ethyl>-4-benzyl-5-(trifluoroacetamido)oxazole 
• 127086-88-8 2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4-<(isopropoxycarbonyl)methyl>phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole 
• 127086-89-9 2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole 
• 127102-45-8 1-benzyl-2-(tert-butyloxycarbonyl)-8(R)--7(R)-phenyl-2-aza-5(1,4)-benzena-6-oxa-1(2,5)-oxazolacyclooctaphane 
• 127086-86-6 N-(1-cyano-3-methylphenyl)-2(R)-(N-carbobenzyloxy-N-methylamino)-3(R)-phenyl-3-<4-<(isopropoxycarbonyl)methyl>phenoxy>propanamide 
• 127086-91-3 5-benzyl-8(R)--9(R)-phenyl-4,7-dioxo-3,6-diaza-11-benzena-10-oxacycloundecaphane 
• 127086-84-4 2(S)-(N-carbobenzyloxy-N-methylamino)-3(R)-phenyl-3-<4-<(isopropoxycarbonyl)methyl>phenoxy>-1-(tert-butyldimethylsilyl)propanol 
• 127102-44-7 2(R)-(N-carbobenzyloxy-N-methylamino)-3(R)-phenyl-3-<4-<(isopropoxycarbonyl)methyl>phenoxy>-1-propanocarboxylic acid 
• 127086-85-5 2-(S)-(N-carbobenzyloxy-N-methylamino)-3(R)-phenyl-3-<4-<(isopropoxycarbonyl)methyl>phenoxy>-1-propanol 
• 127086-92-4 (4S,5S)-5-<(benzyloxycarbonyl)(methyl)amino>-2,2-dimethyl-4-phenyl-1,3-dioxan 
• 127086-82-2 (1S,2S)-2-<(benzyloxycarbonyl)(methyl)amino>-1-phenylpropane-1,3-diol 

Relevant articles and documents

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Disclosed herein are methods of treating a patient suffering from a cognitive disorder using compounds of the following formula, Formula (2), wherein the variables have the meaning defined in the specification.

METHODS FOR TREATING COGNITIVE DISORDERS USING 1-BENZYL-1-HYDROXY-2,3-DIAMINO-PROPYL AMINES, 3-BENZYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES AND RELATED COMPOUNDS

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METHODS FOR TREATING CHRONIC PAIN USING 1-BENZYL-1-HYDROXY-2,3-DIAMINO-PROPYL AMINES,3-BENZYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES AND RELATED COMPOUNDS

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Enantioselective Catalysis, 90. - Optically Active Nitrogen Ligands with Dendrimeric Structure

2-Pyridinecarboxaldehyde (1) reacts with (1S,2S)-2-amino-1-phenyl-1,3-propanediol (2) to afford a mixture of the Schiff base 3 and the oxazolidines 3a/3a', 3b/3b', which was reduced with NaBH4 to yield the optically active 2-pyridinylmethylamino alcohol 4