96363-21-2

Basic information

• Product Name: methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate
• Synonyms: methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate
• CAS NO: 96363-21-2
• Molecular Weight: 309.362
• Mol File: 96363-21-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate(96363-21-2)
• EPA Substance Registry System: methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate(96363-21-2)

Safety Data

• Hazardous Substances Data: 96363-21-2(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 131791-82-7 3-amino-3-(4-methoxyphenyl)propionic acid methyl ester 
• 159990-11-1 (R)-2-tert-butoxycarbonylamino-1-methanesulfonyloxy-2-(4-methoxyphenyl)ethane 
• 193073-85-7 methyl (R)-2-((tert-butoxycarbonyl)amino)-2-(4-methoxyphenyl)acetate 
• 159848-75-6 (S)-3-(N-terc-butoxycarbonylamine)-3-(4-methoxyphenyl)propanenitrile 
• 159848-74-5 1,1-dimethylethyl (R)-N-[2-hydroxy-1-(4-methoxyphenyl)-ethyl]carbamate 
• 131690-56-7 (S)-β-amino-β-(4-methoxyphenyl)propionic acid 
• 159990-12-2 (S)-3-tert-Butoxycarbonylamino-3-(4-methoxy-phenyl)-propionic acid 
• 74-88-4 methyl iodide 
• 123-11-5 4-methoxy-benzaldehyde 
• 67-56-1 methanol 
• 96363-20-1 D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoic acid 

Downstream Products

• 159848-82-5 methyl (3S,3'S)-3-<3'-tert-butyldimethylsiloxy-3'-(4-methoxyphenyl)propylamino>-3-(4-methoxyphenyl)propionate 
• 159848-94-9 methyl (3S,3S')-3-<3'-tert-butoxycarbonylamino-3'-(4-methoxyphenyl)propylamino>-3-(4-methoxyphenyl)propionate 
• 159848-84-7 [(S)-3-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-phenyl)-propyl]-[(S)-3-hydroxy-1-(4-methoxy-phenyl)-propyl]-carbamic acid tert-butyl ester 
• 159848-96-1 (3S,3S')-3--3-(4-methoxyphenyl)-1-propanol 
• 159848-83-6 methyl (3S,3'S)-3--3-(4-methoxyphenyl)propionate 
• 159848-86-9 (3S,3'S)-3--3-(4-methoxyphenyl)-1-(2,2,2-trichloroethoxycarbonyloxy)propane 
• 159848-95-0 methyl (3S,3S')-3--3-(4-methoxyphenyl)propionate 
• 159848-87-0 (3S,3'S)-3-<3'-acetoxy-N-tert-butoxycarbonyl-3'-(4-methoxyphenyl)propylamino>-3-(4-methoxyphenyl)-1-(2,2,2-trichloroethoxycarbonyloxy)propane 
• 159848-97-2 (3S,3S')-3--3-(4-methoxyphenyl)-1-(2,2,2-trichloroethoxycarbonyloxy)propane 
• 159848-85-8 (3S,3'S)-3--3-(4-methoxyphenyl)-1-(2,2,2-trichloroethoxycarbonyloxy)propane 
• 96363-23-4 (1S)-D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)<1-2H>propanol 
• 96363-23-4 (1R)-D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)<1-2H>propanol 
• 96363-29-0 (1S)-D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)<1-2H>propyl propanoate 
• 96363-29-0 C₁₈H₂₆⁽²⁾HNO₅ 

Relevant articles and documents

Synthesis of macrocycles containing 1,3,4-oxadiazole and pyridine moieties

A series of peptide-like 25-28 membered macrocycles containing 1,3,4-oxadiazoles and pyridines bearing a chiral center scaffold have been synthesized by using known coupling reagents and common protecting groups. The yield of the purified macrocycles was poor on an average, yet it seems to be independent of amino acid substitution or stereochemistry. These macrocycles represent a new class of structures for further development and for future application in high-throughput screening against a variety of biological targets.

Synthesis of (4R)-D,L-- and (4S)-D,L-Homoserine Lactones

The (4R)-D,L-- and (4S)-D,L-homoserine lactone hydrochloride salts were prepared from D,L-3-amino-3-(4-methoxyphenyl)propanoic acid (1) in eight steps in an overall yields of 5.0percent.Amino acid 1 was converted into D,L-3-(1,1-dimethyletho