761460-02-0

Basic information

• Product Name: tert-butyl 3-(2-ethoxy-2-oxoethyl)Morpholine-4- carboxylate
• Synonyms: tert-butyl 3-(2-ethoxy-2-oxoethyl)Morpholine-4- carboxylate
• CAS NO: 761460-02-0
• Molecular Formula: C₁₃H₂₃NO₅
• Molecular Weight: 273.32542
• Mol File: 761460-02-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: tert-butyl 3-(2-ethoxy-2-oxoethyl)Morpholine-4- carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 3-(2-ethoxy-2-oxoethyl)Morpholine-4- carboxylate(761460-02-0)
• EPA Substance Registry System: tert-butyl 3-(2-ethoxy-2-oxoethyl)Morpholine-4- carboxylate(761460-02-0)

Safety Data

• Hazardous Substances Data: 761460-02-0(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 81684-84-6 ethyl 2-(morpholin-3-yl)acetate 
• 1071-46-1 hydrogen ethyl malonate 
• 813433-72-6 (4-formyl-morpholin-3-yl)-acetic acid 
• 64-17-5 ethanol 
• 86236-84-2 2-(morpholin-3-yl)acetic acid 

Downstream Products

• 1398397-37-9 methyl 3-(3-(2-(((R)-1-(naphthalen-1-yl)ethyl)amino)ethyl)morpholino)-5-(trifluoromethyl)benzoate 
• 1398397-43-7 methyl 3-(3-(2-(((R)-1-(naphthalen-1-yl)ethyl)amino)ethyl)morpholino)-5-(trifluoromethyl)benzoate 
• 859155-89-8 2-(4-(tert-butoxycarbonyl)morpholin-3-yl)acetic acid 
• 761460-03-1 (3R)-4-tert-butoxycarbonyl-3-carboxymethylmorpholine 
• 761460-04-2 (3S)-4-tert-butoxycarbonyl-3-carbethoxymethylmorpholine 
• 761460-03-1 ((3S)-4-(tert-butoxycarbonyl)morpholin-3-yl)acetic acid 
• 813433-76-0 (5S)-N-tert-butoxycarbonyl-5-(2-hydroxyethyl)morpholine 

Relevant articles and documents

SUBSTITUTED MORPHOLINES AS MODULATORS FOR THE CALCIUM SENSING RECEPTOR

Compounds of Formula (I) along with processes for their preparation that are useful for treating, managing and/or lessening the diseases, disorders, syndromes or conditions associated with the modulation of calcium sensing (CaSR) receptors. Methods of treating, managing and/or lessening the diseases, disorders, syndromes or conditions associated with the modulation of calcium sensing (CaSR) receptors of Formula (I).

Process for producing enantiopure beta-amino acid derivatives, and enantiopure beta-amino acid derivatives

Process for producing enantiopure β-amino acid derivatives corresponding to general formula (I) R1-NZ-CHR2—CH2—COOR3 (I) in which R1 and R2 independently denote organic residues optionally forming a cyclic substituent, R3 denotes H or an organic residue, and Z represents H or an amino function-protecting group, comprising a step in which a mixture of enantiomers of a compound corresponding to general formula (II) R1-NZ-CHR2—CH2—COOR4 (II) in which R1, R2 and Z are as defined for formula (I), and R4 is an organic residue, is subjected to hydrolysis in the presence of a lipase.