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CAS: 23159-09-3
IUPAC Name: 
benzyl N-[2-(dimethylcarbamoyl)ethyl]carbamate
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Enamine Ltd.
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Zoom the structure CSSS00011295704 Add to cart
CAS: 2249432-91-3
IUPAC Name: 
benzyl N-{2-[(3-methyl-1,2,4-thiadiazol-5-yl)amino]ethyl}carbamate
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UORSY
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Zoom the structure CSSS00113620563 Add to cart
CAS: 1427964-37-1
IUPAC Name: 
benzyl N-{2-[(3-methylbutyl)sulfamoyl]ethyl}carbamate
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CAS: 2637216-05-6
IUPAC Name: 
benzyl N-(2-{[4-(morpholine-4-carbonyl)piperazine-1-carbonyl]amino}ethyl)carbamate
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CAS: 58933-52-1
IUPAC Name: 
4-({[(benzyloxy)carbonyl]amino}methyl)benzoic acid
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FCH Group
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Key Organics Limited (BIONET)
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Princeton Biomolecular Research
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Targetmol Chemicals Inc
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Description: 4-(Benzyloxycarbonylamino-methyl)-benzoic acid ,with CAS No. 58933-52-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 4-(Benzyloxycarbonylamino-methyl)-benzoic acid provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.; CAS: 58933-52-1
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Zoom the structure CSSS00000235997 Add to cart
IUPAC Name: 
benzyl N-[(propylcarbamoyl)methyl]carbamate
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Princeton Biomolecular Research
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IUPAC Name: 
3-phenylpropyl N-phenylcarbamate
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Description: Name: 3-phenylpropyl phenylcarbamate; Stereochemistry: achiral; Compound state: solid
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Zoom the structure CSSS00132342836 Add to cart
CAS: 260262-86-0
IUPAC Name: 
benzyl N-(pyridin-4-yl)carbamate
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Princeton Biomolecular Research
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Zoom the structure CSSS00011198257 Add to cart
IUPAC Name: 
N-[2-(benzyloxy)ethyl]furan-2-carboxamide
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Description: Name: N-[2-(benzyloxy)ethyl]-2-furamide; Stereochemistry: achiral; Compound state: solid
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Zoom the structure CSSS00016888304 Add to cart
CAS: 23434-37-9
IUPAC Name: 
7-{[(benzyloxy)carbonyl]amino}heptanoic acid
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UORSY
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Enamine Ltd.
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FCH Group
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Description: Names: N-Cbz-7-Aminoheptanoic acid; Product Description: N-Cbz-7-Aminoheptanoic acid is a six carbon linker containing an carboxylic acid (CO2H) group and a benzyl (Cbz) protecting group. The terminal carboxylic acid is reactive with primary amine groups in the presence of activators (e.g. EDC, or HATU) forming a stable amide bond. The benzyl protecting group can be removed via hydrogenolysis to form a free amine. ; Target: Biochemical Assay Reagents; CAS: 23434-37-9
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Description: Names: N-Cbz-7-Aminoheptanoic acid; Product Description: N-Cbz-7-Aminoheptanoic acid is a six carbon linker containing an carboxylic acid (CO2H) group and a benzyl (Cbz) protecting group. The terminal carboxylic acid is reactive with primary amine groups in the presence of activators (e.g. EDC, or HATU) forming a stable amide bond. The benzyl protecting group can be removed via hydrogenolysis to form a free amine. ; Target: Biochemical Assay Reagents; CAS: 23434-37-9
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Zoom the structure CSSS00000236140 Add to cart
CAS: 1947-00-8
IUPAC Name: 
6-{[(benzyloxy)carbonyl]amino}hexanoic acid
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Description: Names: 6-(Benzyloxycarbonylamino)caproic acid; Product Description: 6-(Benzyloxycarbonylamino)caproic acid is a PROTAC linker that can be used in the synthesis of PROTACs.; Target: PROTAC Linkers; CAS: 1947-00-8
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Description: Names: 6-(Benzyloxycarbonylamino)caproic acid; Product Description: 6-(Benzyloxycarbonylamino)caproic acid is a PROTAC linker that can be used in the synthesis of PROTACs.; Target: PROTAC Linkers; CAS: 1947-00-8
Princeton Biomolecular Research
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Zoom the structure CSSS00000235992 Add to cart
CAS: 1676-86-4
IUPAC Name: 
benzyl N-{4-[(4S)-2,5-dioxo-1,3-oxazolidin-4-yl]butyl}carbamate
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Description: Names: N6-Carbobenzoxy-L-lysine N-carboxyanhydride; Product Description: N6-Carbobenzoxy-L-lysine N-carboxyanhydride is a lysine derivative; Target: Amino Acid Derivatives; CAS: 1676-86-4
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Description: Names: N6-Carbobenzoxy-L-lysine N-carboxyanhydride; Product Description: N6-Carbobenzoxy-L-lysine N-carboxyanhydride is a lysine derivative; Target: Amino Acid Derivatives; CAS: 1676-86-4
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Zoom the structure CSSS00020642060 Add to cart
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