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2508-20-5

2508-20-5 | 9H-Fluorene, 2-nitroso-

CAS No: 2508-20-5 Catalog No: AG002QFR MDL No:

Product Description

Catalog Number:
AG002QFR
Chemical Name:
9H-Fluorene, 2-nitroso-
CAS Number:
2508-20-5
Molecular Formula:
C13H9NO
Molecular Weight:
195.2167
IUPAC Name:
2-nitroso-9H-fluorene
InChI:
InChI=1S/C13H9NO/c15-14-11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8H,7H2
InChI Key:
XZWGJDANCSXBDW-UHFFFAOYSA-N
SMILES:
O=Nc1ccc2c(c1)Cc1c2cccc1
UNII:
34E9V9B29K

Properties

Complexity:
253  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
195.068g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
195.221g/mol
Monoisotopic Mass:
195.068g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
29.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.2  

Literature

Title Journal
Cadmium alters the biotransformation of carcinogenic aromatic amines by arylamine N-acetyltransferase xenobiotic-metabolizing enzymes: molecular, cellular, and in vivo studies. Environmental health perspectives 20101201
Isoform-selective inactivation of human arylamine N-acetyltransferases by reactive metabolites of carcinogenic arylamines. Chemical research in toxicology 20091201
Human arylamine N-acetyltransferase 1: in vitro and intracellular inactivation by nitrosoarene metabolites of toxic and carcinogenic arylamines. Chemical research in toxicology 20081001
Aromatic amines in experimental cancer research: tissue-specific effects, an old problem and new solutions. Critical reviews in toxicology 20070301
Mass spectrometric investigation of the mechanism of inactivation of hamster arylamine N-acetyltransferase 1 by N-hydroxy-2-acetylaminofluorene. Chemical research in toxicology 20040301

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