1329422-58-3

Basic information

• Product Name: N-methyliminodiacetyl (1-oxo-4-phenylbutan-2-yl)boronate
• Synonyms: N-methyliminodiacetyl (1-oxo-4-phenylbutan-2-yl)boronate
• CAS NO: 1329422-58-3
• Molecular Weight: 303.123
• Mol File: 1329422-58-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-methyliminodiacetyl (1-oxo-4-phenylbutan-2-yl)boronate(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyliminodiacetyl (1-oxo-4-phenylbutan-2-yl)boronate(1329422-58-3)
• EPA Substance Registry System: N-methyliminodiacetyl (1-oxo-4-phenylbutan-2-yl)boronate(1329422-58-3)

Safety Data

• Hazardous Substances Data: 1329422-58-3(Hazardous Substances Data)

Upstream product

• 1104636-73-8 6-methyl-2-vinyl-1,3,6,2-dioxazaborocane-4,8-dione 

Downstream Products

• 1329422-69-6 (Z)-1-(4-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-1-en-1-yl)pyrrolidin-2-one 
• 1329422-70-9 (Z)-triisopropyl((4-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-1-en-1-yl)oxy)silane 
• 1329422-74-3 (E)-2-morpholino-3-((2-oxopyrrolidin-1-yl)methylene)-5-phenylpentanoic acid 
• 1329422-80-1 (E)-2-(benzylamino)-5-phenyl-3-(((triisopropylsilyl)oxy)methylene)pentanoic acid 
• 1329422-65-2 (E)-N-methyliminodiacetyl (1,1-dibromo-5-phenylpent-1-en-3-yl)boronate 
• 1401572-26-6 4-phenyl-2-methallyl-2-MIDA boryl aldehyde 
• 1401572-25-5 4-phenyl-2-allyl-2-MIDA boryl aldehyde 
• 1380504-36-8 (1-(3-(tert-butyl)ureido)-3-phenylpropyl)boronic acid 
• 1380504-35-7 benzyl (1-(MIDA boryl)-3-phenylpropyl)carbamate 
• 1380504-30-2 1-(1-(MIDA boryl)-3-phenylpropyl)-3-phenylurea 
• 1380504-29-9 1,1-diethyl-3-(1-(MIDA boryl)-3-phenylpropyl)urea 
• 1380504-28-8 1-(tert-butyl)-3-(1-(MIDA boryl)-3-phenylpropyl)urea 
• 4408-64-4 N-methyliminodiacetic acid 
• 1380504-25-5 (1-amino-3-phenylpropyl)boronic acid hydrochloride 

Relevant articles and documents

Interactions of "bora-penicilloates" with serine β-lactamases and DD-peptidases

Specific boronic acids are generally powerful tetrahedral intermediate/transition state analogue inhibitors of serine amidohydrolases. This group of enzymes includes bacterial β-lactamases and DD-peptidases where there has been considerable development of

Amphoteric α-boryl aldehydes

A new class of stable molecules, α-boryl aldehydes, has been prepared from oxiranyl N-methyliminodiacetyl boronates by a 1,2-boryl migration with concomitant epoxide scission. A range of boryl imines, alkenes, alcohols, acids, enol ethers, enamides, and other functionalized boronic acid derivatives that are difficult or impossible to prepare using established protocols can be accessed from α-boryl aldehydes. The chemoselective transformations of these building blocks, including the facile synthesis of functionalized unnatural amino acids from silyloxy and amido vinyl boronates, attest to the potential of α-boryl aldehydes in chemical synthesis.