181523-90-0

Basic information

• Product Name: (N->B)phenyl[N-carbamoylmethyl-aminodiacetate-O,O',N]borane
• Synonyms: (N->B)phenyl[N-carbamoylmethyl-aminodiacetate-O,O',N]borane
• CAS NO: 181523-90-0
• Molecular Weight: 276.057
• Mol File: 181523-90-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (N->B)phenyl[N-carbamoylmethyl-aminodiacetate-O,O',N]borane(CAS DataBase Reference)
• NIST Chemistry Reference: (N->B)phenyl[N-carbamoylmethyl-aminodiacetate-O,O',N]borane(181523-90-0)
• EPA Substance Registry System: (N->B)phenyl[N-carbamoylmethyl-aminodiacetate-O,O',N]borane(181523-90-0)

Safety Data

• Hazardous Substances Data: 181523-90-0(Hazardous Substances Data)

Upstream product

• 109674-44-4 (N->B)-phenyl[iminodiacetate-O,O',N]borane 
• 144-48-9 iodacetamide 

Downstream Products

• 26239-55-4 N-(2-acetamido)-3-iminodiacetic acid 

Relevant articles and documents

Syntheses of (N → B)phenyl[N-alkylaminodiacetate-O,O′,N]boranes

The syntheses of (N → B)phenyl[N-alkylaminodiacetate-O,O′,N]boranes (2 to 6) and their corresponding N-alkylaminodiacetic acids (7 to 10) are reported. All compounds (except 6) were characterized by 1H, 11B (for boron heterocycles), 13C NMR, infrared spectroscopy and mass spectrometry. The 1H NMR spectrum of compound 3 shows that it is a chiral molecule, its structure was determined by homonuclear decoupling experiments, 1H NMR and HETCOR. The study of the intramolecular N → B coordination by dynamic NMR afforded a ΔG? value of 98.4 kJ mol-1 for compound 3. Copyright