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345-83-5

345-83-5 | (4-Fluorophenyl)(phenyl)methanone

CAS No: 345-83-5 Catalog No: AG003LF3 MDL No:MFCD00000352

Product Description

Catalog Number:
AG003LF3
Chemical Name:
(4-Fluorophenyl)(phenyl)methanone
CAS Number:
345-83-5
Molecular Formula:
C13H9FO
Molecular Weight:
200.2084
MDL Number:
MFCD00000352
IUPAC Name:
(4-fluorophenyl)-phenylmethanone
InChI:
InChI=1S/C13H9FO/c14-12-8-6-11(7-9-12)13(15)10-4-2-1-3-5-10/h1-9H
InChI Key:
OGTSHGYHILFRHD-UHFFFAOYSA-N
SMILES:
Fc1ccc(cc1)C(=O)c1ccccc1
EC Number:
206-463-7
NSC Number:
88321

Properties

Complexity:
213  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
200.064g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
200.212g/mol
Monoisotopic Mass:
200.064g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.5  

Literature

Title Journal
Synthesis and structure-activity relationships of benzophenone-bearing diketopiperazine-type anti-microtubule agents. Bioorganic & medicinal chemistry 20120715
The sensitized emission of Eu3+ and Tb3+ by 4-fluorobenzophenone confined in zeolite L microcrystals. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20110401
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
N'-[1-(4-Chloro-phen-yl)ethyl-idene]acetohydrazide. Acta crystallographica. Section E, Structure reports online 20101101
N'-(4-Fluoro-benzyl-idene)acetohydrazide. Acta crystallographica. Section E, Structure reports online 20101101
3-(4-Fluoro-phen-yl)-1-(4-methoxy-phen-yl)prop-2-en-1-one. Acta crystallographica. Section E, Structure reports online 20090601
Successive chain-growth condensation polymerization for the synthesis of well-defined diblock copolymers of aromatic polyamide and aromatic polyether. Macromolecular rapid communications 20090102

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