77835-31-5

Usage

Uses

Used in Pharmaceutical Industry:
BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE is used as a key intermediate in the synthesis of various pharmaceutical compounds, including antibiotics, antiviral agents, and anticancer drugs. Its ability to form polyamines and polyamides allows for the creation of complex molecular structures with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of chemical synthesis, BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE is used as a building block for the preparation of specialty polymers, such as polyamides with unique properties. These polymers can be utilized in various applications, including high-performance materials, coatings, and adhesives.
Used in Research and Development:
BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE is also used as a research compound in academic and industrial laboratories. Its reactivity and functional groups make it a valuable tool for exploring new synthetic routes and developing novel chemical entities with potential applications in various industries.
Overall, BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE is a versatile and valuable chemical compound with applications in the pharmaceutical, chemical synthesis, and research industries, owing to its unique structure and properties as a building block for polyamines and polyamides.

Upstream product

• 142342-55-0 diethyl {5-[(tert-butoxycarbonyl)amino]pentyl }-propanedioate 
• 75178-90-4 N-(tert-butyloxycarbonyl)-5-aminopentanol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 2508-29-4 5-hydroxypentylamine 
• 129392-86-5 (5-azido-pentyl)carbamic acid tert-butyl ester 
• 462-94-2 1,5-diaminopentane 

Downstream Products

• 121903-84-2 2,4-dibenzyloxyphenylacetyl-L-Asn->Cad<-Pua(Z)-H 
• 121903-73-9 [4-({2-[5-((S)-2-Amino-3-carbamoyl-propionylamino)-pentylcarbamoyl]-ethyl}-benzyloxycarbonyl-amino)-butyl]-carbamic acid 2,2,2-trichloro-ethyl ester 
• 121903-77-3 [5-(3-{Benzyloxycarbonyl-[4-(2,2,2-trichloro-ethoxycarbonylamino)-butyl]-amino}-propionylamino)-pentyl]-carbamic acid tert-butyl ester 
• 121903-78-4 (4-{[2-(5-Amino-pentylcarbamoyl)-ethyl]-benzyloxycarbonyl-amino}-butyl)-carbamic acid 2,2,2-trichloro-ethyl ester 
• 121903-76-2 (5-{3-[(4-Amino-butyl)-benzyloxycarbonyl-amino]-propionylamino}-pentyl)-carbamic acid tert-butyl ester 
• 113953-98-3 2,4-dibenzyloxyphenylacetyl-L-Asn->Cad<-Pua(Z)-Troc 
• 113953-97-2 Boc->Cad<-Pua(Z)=Pht 
• 326406-09-1 N-Boc-5-{[(2-aminoanilino)carbothioyl]amino}pentan-1-amine 
• 113953-96-1 Boc->Cad<-Pua(Z)=Pht 
• 1269620-02-1 (R)-benzyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-((5-((tertbutoxycarbonyl)amino)pentyl)amino)-5-oxopentanoate 

Relevant academic research and scientific papers

Total synthesis of nstx-3, spider toxin of Nephila maculata

A spider toxin NSTX-3 obtained from the venom of Papua New Guinean spider, Nephila maculata was synthesized in order to confirm its proposed structure and to supply the sample for the biological tests. The structure of NSTX-3 is now established as 2,4-dihydroxyphenylacetyl-L-Asn→Cad←Pua←L-Arg, where Cad stands for cadaverine and Pua for putreanine.

Mono-Protected Diamines. Nα-tert-Butoxycarbonyl α,ω-Alkanediamine Hydrochlorides from Amino alcohols.

Nα-tert-Butoxycarbonyl α,ω-alkanediamine hydrochlorides 3a-e are prepared from the amino alcohols in yields of 66-87percent.Reaction of the free amine with di-tert-butyl dicarbonate gives the N-tert-Butoxycarbonylamino alcohol 1a-e.One-pot conversion to the azide 2a-e via the mesylate under phase-transfer conditions followed by hydrogenolysis in the presence of chloroform yields the title compounds.