129392-86-5

Basic information

• Product Name: Carbamic acid, (5-azidopentyl)-, 1,1-dimethylethyl ester
• CAS NO: 129392-86-5
• Molecular Formula: C10H20N4O2
• Molecular Weight: 228.294
• Mol File: 129392-86-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Carbamic acid, (5-azidopentyl)-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (5-azidopentyl)-, 1,1-dimethylethyl ester(129392-86-5)
• EPA Substance Registry System: Carbamic acid, (5-azidopentyl)-, 1,1-dimethylethyl ester(129392-86-5)

Safety Data

• Hazardous Substances Data: 129392-86-5(Hazardous Substances Data)

Upstream product

• 51644-96-3 5-tert-butoxycarbonylamino-1-aminopentane 

Downstream Products

• 77835-31-5 N-(tert-butoxycarbonyl)-1,5-diaminopentane hydrochloride 
• 51644-96-3 5-tert-butoxycarbonylamino-1-aminopentane 
• 200066-59-7 (5-{(S)-2-[2-(4-Benzyloxy-1H-indol-3-yl)-acetylamino]-3-carbamoyl-propionylamino}-pentyl)-carbamic acid tert-butyl ester 
• 213821-99-9 C₆₂H₉₇N₁₃O₁₃ 
• 200066-60-0 (3-Azido-propyl)-(4-{[2-(5-{(S)-2-[2-(4-benzyloxy-1H-indol-3-yl)-acetylamino]-3-carbamoyl-propionylamino}-pentylcarbamoyl)-ethyl]-tert-butoxycarbonyl-amino}-butyl)-carbamic acid tert-butyl ester 
• 119613-54-6 NPTX-11 
• 142342-57-2 ((S)-4-tert-Butoxycarbonylamino-4-{5-[(S)-3-carbamoyl-2-(2-1H-indol-3-yl-acetylamino)-propionylamino]-pentylcarbamoyl}-butyl)-carbamic acid benzyl ester 
• 142342-58-3 C₆₂H₇₃N₁₁O₁₃ 
• 1426822-68-5 (9H-fluoren-9-yl)methyl (5-(5-tosyl-1H-tetrazol-1-yl)pentyl)carbamate 

Relevant articles and documents

Chemical probes for the functionalization of polyketide intermediates

A library of functionalized chemical probes capable of reacting with ketosynthase-bound biosynthetic intermediates was prepared and utilized to explore in vivo polyketide diversification. Fermentation of ACP mutants of S. lasaliensis in the presence of the probes generated a range of unnatural polyketide derivatives, including novel putative lasalocid A derivatives characterized by variable aryl ketone moieties and linear polyketide chains (bearing alkyne/azide handles and fluorine) flanking the polyether scaffold. By providing direct information on microorganism tolerance and enzyme processing of unnatural malonyl-ACP analogues, as well as on the amenability of unnatural polyketides to further structural modifications, the chemical probes constitute invaluable tools for the development of novel mutasynthesis and synthetic biology.