Catalog No.:AA003JOH

3468-01-7 | 3-Methylflavone-8-carboxylic acid

Name: Name:3-Methylflavone-8-carboxylic acid
Brand: AABLOCKS
SKU: AA003JOH
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25g

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$21.00 $15.00

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100g

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$60.00 $42.00

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500g

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003JOH

Chemical Name:

3-Methylflavone-8-carboxylic acid

CAS Number:

3468-01-7

Molecular Formula:

C17H12O4

Molecular Weight:

280.2748

MDL Number:

MFCD00040998

SMILES:

OC(=O)c1cccc2c1oc(c1ccccc1)c(c2=O)C

Properties

BP:

485.1°C at 760 mmHg

Form:

Solid

MP:

234-236 °C

Storage:

Keep in dry area;2-8℃;

Computed Properties

Complexity:

473

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

3.4

Downstream Synthesis Route

3468-01-7

5472-49-1

3-(1-piperidinyl)propyl2-phenyl-3-methyl-4-oxo-4H-1-benzopyran-8-carboxylate

[1]Nardi;Leonardi;Pennini;Tajana;Cazzulani;Testa[Arzneimittel-Forschung/DrugResearch,1993,vol.43,#1,p.28-34]

103085-54-7

3468-01-7

[1]Uneyama,Kenji;Masatsugu,Yosinori;Torii,Sigeru[BulletinoftheChemicalSocietyofJapan,1985,vol.58,#8,p.2361-2365]

[2]Uneyama,Kenji;Masatsugu,Yosinori;Torii,Sigeru[BulletinoftheChemicalSocietyofJapan,1985,vol.58,#8,p.2361-2365]

14365-73-2

3468-01-7

(2S,3S,4S,5R,6R)-3,4,5-Triacetoxy-6-(3-methyl-4-oxo-2-phenyl-4H-chromene-8-carbonyl)-amino-tetrahydro-pyran-2-carboxylicacidmethylester

[1]Pitt,Nigel;Duane,RhonaM.;O'Brien,Alan;Bradley,Helena;Wilson,StephenJ.;O'Boyle,KathyM.;Murphy,PaulV.[CarbohydrateResearch,2004,vol.339,#11,p.1873-1887]

3468-01-7

1-deoxy-1-(3-methyl-4-oxo-2-phenyl-4H-1-benzopyran-8-yl)carbonylamino}-β-D-glucopyranuronicacid

[1]Pitt,Nigel;Duane,RhonaM.;O'Brien,Alan;Bradley,Helena;Wilson,StephenJ.;O'Boyle,KathyM.;Murphy,PaulV.[CarbohydrateResearch,2004,vol.339,#11,p.1873-1887]

Literature

Title: Molecularly imprinted polymer for selective extraction of 3-methylflavone-8-carboxylic acid from human urine followed by its determination using zwitterionic hydrophilic interaction liquid chromatography.

Journal: Journal of separation science 20111101

Title: Relationship between the structures of flavonoids and their NF-κB-dependent transcriptional activities.

Journal: Bioorganic & medicinal chemistry letters 20111015

Title: Liquid Chromatographic Determination of Flavoxate HCl in Pharmaceutical Formulation.

Journal: Journal of young pharmacists : JYP 20100101

Title: Liquid chromatographic fingerprint of 3-methylflavone-8-carboxylic acid established for its synthesis control analysis.

Journal: Talanta 20090315

Title: High-performance liquid chromatographic determination of flavoxate hydrochloride and its hydrolysis product.

Journal: Drug development and industrial pharmacy 20081201

Title: 3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic acid.

Journal: Acta crystallographica. Section E, Structure reports online 20080501

Title: High performance liquid chromatographic determination of 3-methylflavone-8-carboxylic acid, the main active metabolite of flavoxate hydrochloride in human urine.

Journal: Journal of pharmaceutical and biomedical analysis 20070509

Title: Fatty acid synthase inhibitors from plants: isolation, structure elucidation, and SAR studies.

Journal: Journal of natural products 20021201

Title: Development of a high-performance liquid chromatographic method for bioequivalence study of flavoxate tablets.

Journal: Journal of chromatography. B, Biomedical sciences and applications 20010210

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