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156489-35-9

156489-35-9 | 9H-Purin-2-amine, 6-(2-thienyl)-

CAS No: 156489-35-9 Catalog No: AG001OR3 MDL No:

Product Description

Catalog Number:
AG001OR3
Chemical Name:
9H-Purin-2-amine, 6-(2-thienyl)-
CAS Number:
156489-35-9
Molecular Formula:
C9H7N5S
Molecular Weight:
217.2504
IUPAC Name:
6-thiophen-2-yl-7H-purin-2-amine
InChI:
InChI=1S/C9H7N5S/c10-9-13-6(5-2-1-3-15-5)7-8(14-9)12-4-11-7/h1-4H,(H3,10,11,12,13,14)
InChI Key:
QCHLWIPINNRBSG-UHFFFAOYSA-N
SMILES:
Nc1nc(c2cccs2)c2c(n1)[nH]cn2

Properties

Complexity:
239  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
217.042g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
217.25g/mol
Monoisotopic Mass:
217.042g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
109A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.1  

Literature

Title Journal
Site-specific fluorescent probing of RNA molecules by unnatural base-pair transcription for local structural conformation analysis. Nature protocols 20100701
Cytostatic evaluations of nucleoside analogs related to unnatural base pairs for a genetic expansion system. Bioorganic & medicinal chemistry letters 20071015
Site-specific fluorescent labeling of RNA molecules by specific transcription using unnatural base pairs. Journal of the American Chemical Society 20051214
Non-hydrogen-bonded base pairs for specific transcription. Nucleic acids symposium series (2004) 20050101
Fluorescent properties of an unnatural nucleobase, 2-amino-6-(2-thienyl)purine, in DNA and RNA fragments. Nucleic acids symposium series (2004) 20050101
Site-specific incorporation of fluorescent probes into RNA by specific transcription using unnatural base pairs. Nucleic acids symposium series (2004) 20050101
A two-unnatural-base-pair system toward the expansion of the genetic code. Journal of the American Chemical Society 20041020
Unnatural base pairs between 2- and 6-substituted purines and 2-oxo(1H)pyridine for expansion of the genetic alphabet. Bioorganic & medicinal chemistry letters 20041004
Unnatural base pairs mediate the site-specific incorporation of an unnatural hydrophobic component into RNA transcripts. Bioorganic & medicinal chemistry letters 20040517
Site-specific incorporation of a photo-crosslinking component into RNA by T7 transcription mediated by unnatural base pairs. Chemistry & biology 20040101
Site-specific fluorescent labeling of RNA by a base-pair expanded transcription system. Nucleic acids symposium series (2004) 20040101
An unnatural base pair for efficient incorporation of nucleotide analogs into RNAs. Nucleic acids research. Supplement (2001) 20030101
Simple preparation of biotinylated RNA by transcription via an unnatural base pair. Nucleic acids research. Supplement (2001) 20030101
An unnatural base pair for incorporating amino acid analogs into proteins. Nature biotechnology 20020201
An unnatural base pair between imidazolin-2-one and 2-amino-6-(2-thienyl)purine in replication and transcription. Nucleic acids research. Supplement (2001) 20020101
Synthesis of 6-(2-thienyl)purine nucleoside derivatives that form unnatural base pairs with pyridin-2-one nucleosides. Bioorganic & medicinal chemistry letters 20010820

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