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Home Amines 28128-33-8
28128-33-8,MFCD18252947
Catalog No.:AA00C4FY

28128-33-8 | 1H-Purine-6,8-diamine (9CI)

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10mg
≥98%(HPLC)
in stock  
$188.00   $132.00
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50mg
≥98%(HPLC)
in stock  
$615.00   $430.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00C4FY
Chemical Name:
1H-Purine-6,8-diamine (9CI)
CAS Number:
28128-33-8
Molecular Formula:
C5H6N6
Molecular Weight:
150.1413
MDL Number:
MFCD18252947
SMILES:
Nc1[nH]c2c(n1)ncnc2N
NSC Number:
21698
Properties
Computed Properties
 
Complexity:
150  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
XLogP3:
-0.6  

Downstream Synthesis Route
28128-33-8    129940-50-7   
(S)-8-Amino-9-2-hydroxy-3-(trityloxy)propyladenine 

[1]CollectionofCzechoslovakChemicalCommunications,2001,vol.66,p.517-532

[1]Nucleosides,nucleotidesandnucleicacids,2001,vol.20,p.1103-1106

[2]JournalofMedicinalChemistry,1990,vol.33,p.2073-2080

Literature

Title: Synthesis of cyclic adenosine 5'-diphosphate ribose analogues: a C2'endo/syn 'southern' ribose conformation underlies activity at the sea urchin cADPR receptor.

Journal: Organic & biomolecular chemistry 20110107

Title: Structural properties of g,t-parallel duplexes.

Journal: Journal of nucleic acids 20100101

Title: Structure-activity relationships of adenine and deazaadenine derivatives as ligands for adenine receptors, a new purinergic receptor family.

Journal: Journal of medicinal chemistry 20091008

Title: Property editing of peptide nucleic acids (PNA): gem-dimethyl, cyanuryl and 8-aminoadenine PNAs.

Journal: Nucleic acids symposium series (2004) 20070101

Title: Convenient synthesis of 8-amino-2'-deoxyadenosine.

Journal: Nucleosides, nucleotides & nucleic acids 20030201

Title: Parallel-stranded hairpins containing 8-aminopurines. Novel efficient probes for triple-helix formation.

Journal: Bioorganic & medicinal chemistry letters 20010709

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SDS
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