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642-29-5 | Naphthalen-1-yl(phenyl)methanone
CAS No: 642-29-5 Catalog No: AG003EJO MDL No:MFCD00046431
Product Description
Catalog Number:
AG003EJO
Chemical Name:
Naphthalen-1-yl(phenyl)methanone
CAS Number:
642-29-5
Molecular Formula:
C17H12O
Molecular Weight:
232.2766
MDL Number:
MFCD00046431
IUPAC Name:
naphthalen-1-yl(phenyl)methanone
InChI:
InChI=1S/C17H12O/c18-17(14-8-2-1-3-9-14)16-12-6-10-13-7-4-5-11-15(13)16/h1-12H
InChI Key:
CXAYOCVHDCXPAI-UHFFFAOYSA-N
SMILES:
O=C(c1cccc2c1cccc2)c1ccccc1
EC Number:
211-382-5
NSC Number:
6729
Properties
Complexity:
290
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
232.089g/mol
Formal Charge:
0
Heavy Atom Count:
18
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
232.282g/mol
Monoisotopic Mass:
232.089g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.5
Literature
| Title | Journal |
|---|---|
| Synthesis of gallic acid based naphthophenone fatty acid amides as cathepsin D inhibitors. | Bioorganic & medicinal chemistry letters 20060901 |
| Synthesis of aromatic ketones by a transition metal-catalyzed tandem sequence. | Journal of the American Chemical Society 20060614 |
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. | Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501 |
| Synthesis of 1-(3',4',5'-trimethoxy) phenyl naphtho[2,1b]furan as a novel anticancer agent. | Bioorganic & medicinal chemistry letters 20060215 |
| Properties of excited ketyl radicals of benzophenone analogues affected by the size and electronic character of the aromatic ring systems. | Chemistry (Weinheim an der Bergstrasse, Germany) 20060208 |
| Synthesis of a novel plant growth promoter from gallic acid. | Bioorganic & medicinal chemistry letters 20050215 |
| Molecular recognition by wall-assembling-type nanocavity in aqueous media. | Journal of nanoscience and nanotechnology 20020201 |
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