Home Other Building Blocks 7-Methoxy-2-phenylchroman-4-one

7-Methoxy-2-phenylchroman-4-one

CAS No.:
21785-09-1
Catalog Number:
AG003NGA
Molecular Formula:
C16H14O3
Molecular Weight:
254.2806
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
Product Description
Catalog Number:
AG003NGA
Chemical Name:
7-Methoxy-2-phenylchroman-4-one
CAS Number:
21785-09-1
Molecular Formula:
C16H14O3
Molecular Weight:
254.2806
MDL Number:
MFCD00017486
IUPAC Name:
7-methoxy-2-phenyl-2,3-dihydrochromen-4-one
InChI:
InChI=1S/C16H14O3/c1-18-12-7-8-13-14(17)10-15(19-16(13)9-12)11-5-3-2-4-6-11/h2-9,15H,10H2,1H3
InChI Key:
VYESEQLQFXUROZ-UHFFFAOYSA-N
SMILES:
COc1ccc2c(c1)OC(CC2=O)c1ccccc1
Properties
Complexity:
322  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
254.094g/mol
Formal Charge:
0
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
254.285g/mol
Monoisotopic Mass:
254.094g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
35.5A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
2.9  
Literature
Title Journal
Evaluation of novel amylose and cellulose-based chiral stationary phases for the stereoisomer separation of flavanones by means of nano-liquid chromatography. Analytica chimica acta 20120813
Microbial transformations of 7-hydroxyflavanone. TheScientificWorldJournal 20120101
Racemic tricarbon-yl[7-meth-oxy-2-(η-phen-yl)chromane]-chromium(0). Acta crystallographica. Section E, Structure reports online 20110401
Racemic tricarbon-yl(η-7-meth-oxy-flavan)chromium(0). Acta crystallographica. Section E, Structure reports online 20100801
Optical isomer separation of flavanones and flavanone glycosides by nano-liquid chromatography using a phenyl-carbamate-propyl-beta-cyclodextrin chiral stationary phase. Journal of chromatography. A 20100212
A new series of flavones, thioflavones, and flavanones as selective monoamine oxidase-B inhibitors. Bioorganic & medicinal chemistry 20100201
Microbial transformation of selected flavanones as a method of increasing the antioxidant properties. Zeitschrift fur Naturforschung. C, Journal of biosciences 20100101
Effect of flavonoids on androgen and glucocorticoid receptors based on in vitro reporter gene assay. Bioorganic & medicinal chemistry letters 20090815
Relationships between the structures of flavanone derivatives and their effects in enhancing early growth response-1 gene expression. Bioorganic & medicinal chemistry letters 20090415
Determination of seven flavonoids in Ixeridium gracile (DC.) Shih by high-performance liquid chromatography. Journal of AOAC International 20090101
[Chemical constituents of Oxytropis falcate]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20080601
New 7,8-benzoflavanones as potent aromatase inhibitors: synthesis and biological evaluation. Bioorganic & medicinal chemistry 20080201
Design, synthesis and evaluation of 4-imidazolylflavans as new leads for aromatase inhibition. Bioorganic & medicinal chemistry letters 20021021
Enantiomer separation of flavour and fragrance compounds by liquid chromatography using novel urea-covalent bonded methylated beta-cyclodextrins on silica. Journal of chromatography. A 20020830
New aromatase inhibitors. Synthesis and inhibitory activity of pyridinyl-substituted flavanone derivatives. Bioorganic & medicinal chemistry letters 20020408
Properties