2076-44-0

Basic information

• Product Name: L-erythro β-Hydroxynorleucine
• CAS NO: 2076-44-0
• Molecular Weight: 147.174
• Mol File: 2076-44-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: L-erythro β-Hydroxynorleucine(CAS DataBase Reference)
• NIST Chemistry Reference: L-erythro β-Hydroxynorleucine(2076-44-0)
• EPA Substance Registry System: L-erythro β-Hydroxynorleucine(2076-44-0)

Safety Data

• Hazardous Substances Data: 2076-44-0(Hazardous Substances Data)

Upstream product

• 113951-20-5 (+/-)-erythro-2-acetylamino-3-hydroxy-hexanoic acid ethyl ester 
• 129274-25-5 (5S,6R)-3-(1-Hydroxy-butyl)-2-oxo-5,6-diphenyl-morpholine-4-carboxylic acid benzyl ester 
• 13419-69-7 (E)-2-Hexenoic acid 
• 2076-44-0 (+/-)-erythro-2-amino-3-hydroxy-hexanoic acid 
• 32817-15-5 copper(II) glycinate 
• 123-72-8 butyraldehyde 

Downstream Products

• 108488-46-6 (+/-)-threo-3-hydroxy-2-(4-nitro-benzoylamino)-hexanoic acid 
• 2076-44-0 (+/-)-threo-2-amino-3-hydroxy-hexanoic acid 
• 108488-46-6 (+/-)-erythro-3-hydroxy-2-(4-nitro-benzoylamino)-hexanoic acid 
• 108924-77-2 (+/-)-erythro-3-hydroxy-2-(toluene-4-sulfonylamino)-hexanoic acid 

Relevant articles and documents

ASYMMETRIC ALDOL REACTIONS USING BORON ENOLATES OF CHIRAL OXAZINONES, SYNTHESIS OF L-ALLO-THREONINE

The boron enolate of oxazinone 1 was allowed to react with acetaldehyde, butanal, and 2-methylpropanal.The reaction proceeded stereoselectively, and in the reaction with acetaldehyde, the reaction afforded a precursor to L-allo-threonine.