1352721-81-3

Basic information

• Product Name: methyl 2-(N-tert-butoxycarbonylamino)-2-(2-methoxylphenyl)acetate
• CAS NO: 1352721-81-3
• Molecular Weight: 295.335
• Mol File: 1352721-81-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 2-(N-tert-butoxycarbonylamino)-2-(2-methoxylphenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(N-tert-butoxycarbonylamino)-2-(2-methoxylphenyl)acetate(1352721-81-3)
• EPA Substance Registry System: methyl 2-(N-tert-butoxycarbonylamino)-2-(2-methoxylphenyl)acetate(1352721-81-3)

Safety Data

• Hazardous Substances Data: 1352721-81-3(Hazardous Substances Data)

Upstream product

• 4248-19-5 tert-butyl carbazate 
• 135-02-4 ortho-anisaldehyde 
• 1291065-82-1 C₂₅H₄₅NO₃Sn 
• 179417-69-7 tert-butoxy-carbonylamino-(2-methoxy-phenyl)-acetic acid 
• 18107-18-1 diazomethyl-trimethyl-silane 

Relevant articles and documents

One-pot synthesis of α-amino acids from CO2 using a bismetal reagent with Si-B bond

In the presence of 1.1 equiv of PhMe2Si-Bpin, 5 equiv of CsF, and 20 mol % of TsOH·H2O, precursors of N-Boc-imines can be converted into the corresponding α-aryl or α-alkenyl glycine derivatives under gaseous CO2 in moderate-to-high yields with a single operation. α-Isobutenyl glycine thus obtained can be further derivatized into various types of α-amino acids including N-Boc-leucine, serine, and glycine derivatives in short steps.