1026885-57-3

Basic information

• Product Name: 3-{[(2-amino-3-carboxy-propionyl)-methyl-amino]-methyl}-4-iodo-benzoic acid tert-butyl ester
• CAS NO: 1026885-57-3
• Molecular Weight: 462.285
• Mol File: 1026885-57-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-{[(2-amino-3-carboxy-propionyl)-methyl-amino]-methyl}-4-iodo-benzoic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-{[(2-amino-3-carboxy-propionyl)-methyl-amino]-methyl}-4-iodo-benzoic acid tert-butyl ester(1026885-57-3)
• EPA Substance Registry System: 3-{[(2-amino-3-carboxy-propionyl)-methyl-amino]-methyl}-4-iodo-benzoic acid tert-butyl ester(1026885-57-3)

Safety Data

• Hazardous Substances Data: 1026885-57-3(Hazardous Substances Data)

Upstream product

• 360059-34-3 tert-butyl 4-iodo-3-methylaminomethylbenzoate 
• 360059-33-2 tert-butyl 4-iodo-3-methyl-benzoate 
• 52107-87-6 4-iodo-3-methylbenzoic acid 
• 360059-35-4 (S)-tert-butyl 3-(N-Fmoc-aspartate-β-methyl ester-N-methyl)-amino-methyl-4-iodo-benzoate 

Downstream Products

• 171049-14-2 lotrafiban 

Relevant articles and documents

CuI-catalyzed coupling reaction of beta-amino acids or esters with aryl halides at temperature lower than that employed in the normal Ullmann reaction. Facile synthesis of SB-214857.

[reaction: see text] The CuI-catalyzed coupling reaction of aryl halides with beta-amino acids or beta-amino esters is completed at 100 degrees C in 48 h, which indicates that the structure of the beta-amino acid has an accelerating effect for the Ullmann