4512-41-8

Basic information

• Product Name: 2-<2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-2-methylpropionamido>-2-methylpropionsaeure
• Synonyms: 2-<2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-2-methylpropionamido>-2-methylpropionsaeure
• CAS NO: 4512-41-8
• Molecular Weight: 407.467
• Mol File: 4512-41-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-<2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-2-methylpropionamido>-2-methylpropionsaeure(CAS DataBase Reference)
• NIST Chemistry Reference: 2-<2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-2-methylpropionamido>-2-methylpropionsaeure(4512-41-8)
• EPA Substance Registry System: 2-<2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-2-methylpropionamido>-2-methylpropionsaeure(4512-41-8)

Safety Data

• Hazardous Substances Data: 4512-41-8(Hazardous Substances Data)

Upstream product

• 83537-94-4 Benzyloxycarbonyl-α-aminoisobutyryl-α-aminoisobutyric acid tert butyl ester 
• 1312775-18-0 N-[benzyloxycarbonyl]-2-methylalanyl-2-methylalanyl-2-methylalanine-N-methyl-N-phenylamide 
• 1312775-17-9 N-[benzyloxycarbonyl]-2-methylalanyl-2-methylalanine-N-methyl-N-phenylamide 
• 111492-19-4 2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-N,N,2-trimethylpropionamid 
• 501-53-1 benzyl chloroformate 
• 79775-03-4 2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-2-methylpropionsaeure 
• 15030-72-5 Z-Aib-OH 
• 111492-32-1 2-<2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-2-methylpropionamido>-N,N,2-trimethylpropionamid 

Downstream Products

• 1312775-30-6 N-[benzyloxycarbonyl]-2-methylalanyl-2-methylalanyl-2-methylalanyl-L-prolyl-2-methylalanyl-2-methylalanyl-2-methylalanine-N-methyl-N-phenylamide 
• 1312775-20-4 N-[benzyloxycarbonyl]-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanine-N-methyl-N-phenylamide 
• 1312883-24-1 N-[benzyloxycarbonyl]-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanine-N-methyl-N-phenylamide 
• 4512-42-9 N-[benzyloxycarbonyl]-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanine 
• 4512-43-0 N-[benzyloxycarbonyl]-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanine 
• 1312883-23-0 N-[benzyloxycarbonyl]-2-methylalanyl-2-methylalanyl-2-methylalanyl-2-methylalanine-N-methyl-N-phenylamide 
• 4512-33-8 {1-[1-(4,4-dimethyl-5-oxo-4,5-dihydro-oxazol-2-yl)-1-methyl-ethylcarbamoyl]-1-methyl-ethyl}-carbamic acid benzyl ester 
• 4512-40-7 Z-(Aib)6-OtBu 
• 4512-44-1 Z-(Aib)6-OH 
• 111492-33-2 2-<2-<2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-2-methylpropionamido>-2-methylpropionamido>-N,N,2-trimethylpropionamid 

Relevant articles and documents

Helical Peptides Design for Molecular Dipoles Functionalization of Wide Band Gap Oxides

The use of helical hexapeptides to establish a surface dipole layer on a TiO2 substrate, with the goal of influencing the energy levels of a coadsorbed chromophore, is explored. Two helical hexapeptides, synthesized from 2-amino isobutyric acid

3-(Dimethylamino)-2,2-dimethyl-2H-azirine as an Aib Equivalent; Synthesis of Aib Oligopeptides

3-(Dimethylamino)-2,2-dimethyl-2H-azirine (1) reacts with carboxylic acids at 0-25 degC to give 2-acylamino-N,N,2-trimethylpropionamides (=2-acylamino-N,N-dimethylisobutyramide, acyl-Aib-NMe2) in excellent yields (Scheme 2 and 3).Examples of α-amino-, α-h