Unusual Amino Acids and Derivatives

Features and Benefits Efficient chemiluminescent NH 2 -coupling reagent for detection of a wide variety of proteins down to the picomole range. Other Notes Reportedly, the use of this material in chemiluminescent assays has distinct advantages over

Features and Benefits Efficient chemiluminescent NH 2 -coupling reagent for detection of a wide variety of proteins down to the picomole range. Other Notes Reportedly, the use of this material in chemiluminescent assays has distinct advantages over

N-(4-Bromophenyl)-N’-Ethyl Urea.

N-(4-Bromophenyl)-N’-Ethyl Urea.

Application Schiff base which can be converted to amino alcohols and amino esters.

Application Schiff base which can be converted to amino alcohols and amino esters.

N-(Phenylsulfonyl)glycine Methyl Ester.

N-(Phenylsulfonyl)glycine Methyl Ester.

N-(tert-Butoxycarbonyl)-D-2-(4-chlorophenyl)glycine.

Application &#945-Amino Weinreb amide.

N-[(2S,3R)-3-Amino-2-hydroxy-4-phenylbutyryl]-L-leucine

N-[(adamantan-1-yl)methyl]-2-chloro-5-{3-[(3-hydroxypropyl)amino]propyl}benzamide.