126402-92-4

Basic information

• Product Name: 2,2-Dimethyl-propionic acid (2S,3S,4R,5R)-2-{[(S)-tert-butylcarbamoyl-(4-chloro-phenyl)-methyl]-formyl-amino}-4,5-bis-(2,2-dimethyl-propionyloxy)-tetrahydro-pyran-3-yl ester
• Synonyms: 2,2-Dimethyl-propionic acid (2S,3S,4R,5R)-2-{[(S)-tert-butylcarbamoyl-(4-chloro-phenyl)-methyl]-formyl-amino}-4,5-bis-(2,2-dimethyl-propionyloxy)-tetrahydro-pyran-3-yl ester
• CAS NO: 126402-92-4
• Molecular Weight: 653.213
• Mol File: 126402-92-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,2-Dimethyl-propionic acid (2S,3S,4R,5R)-2-{[(S)-tert-butylcarbamoyl-(4-chloro-phenyl)-methyl]-formyl-amino}-4,5-bis-(2,2-dimethyl-propionyloxy)-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-Dimethyl-propionic acid (2S,3S,4R,5R)-2-{[(S)-tert-butylcarbamoyl-(4-chloro-phenyl)-methyl]-formyl-amino}-4,5-bis-(2,2-dimethyl-propionyloxy)-tetrahydro-pyran-3-yl ester(126402-92-4)
• EPA Substance Registry System: 2,2-Dimethyl-propionic acid (2S,3S,4R,5R)-2-{[(S)-tert-butylcarbamoyl-(4-chloro-phenyl)-methyl]-formyl-amino}-4,5-bis-(2,2-dimethyl-propionyloxy)-tetrahydro-pyran-3-yl ester(126402-92-4)

Safety Data

• Hazardous Substances Data: 126402-92-4(Hazardous Substances Data)

Upstream product

• 64-18-6 formic acid 
• 119072-55-8 tert-butylisonitrile 
• 104-88-1 4-chlorobenzaldehyde 
• 126402-89-9 2,3,4-tri-O-pivaloyl-β-D-arabinopyranosylamine 
• 138892-04-3 α-D-Arabinopyranosyl azide 
• 138891-96-0 2,3,4-Tri-O-pivaloyl-α-D-arabinopyranosyl azide 

Downstream Products

• 67336-19-0 (S)-2-amino-2-(4-chlorophenyl)acetic acid 
• 138892-03-2 2,3,4-Tri-O-pivaloyl-α,β-arabinopyranose 
• 126402-96-8 (S)-2-Amino-N-tert-butyl-2-(4-chloro-phenyl)-acetamide; hydrochloride 

Relevant articles and documents

CARBOHYDRATES AS CHIRAL TEMPLATES: DIASTEREOSELECTIVE UGI SYNTHESIS OF (S)-AMINO ACIDS USING O-ACYLATED D-ARABINOPYRANOSYLAMINE AS THE AUXILIARY

Enantiomerically pure (S)-amino acids are synthesized via a highly diastereoselective Ugi reaction using 2,3,4-tri-O-pivaloyl-α-D-arabinopyranosylamine as the chiral template.