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Factory supply 6-HYDROXYFLAVONE 6665-83-4 with sufficient stock and high standard

  • Molecular Formula: C15H10O3
  • Molecular Weight: 238.243
  • Appearance/Colour: light yellow crystals 
  • Vapor Pressure: 1.02E-08mmHg at 25°C 
  • Melting Point: 234-236 °C(lit.) 
  • Refractive Index: 1.666 
  • Boiling Point: 450.1 °C at 760 mmHg 
  • PKA: 8.98±0.40(Predicted) 
  • Flash Point: 176.3 °C 
  • PSA: 50.44000 
  • Density: 1.34 g/cm3 
  • LogP: 3.16560 

6-HYDROXYFLAVONE(Cas 6665-83-4) Usage

Synthesis Reference(s)

Tetrahedron Letters, 27, p. 2751, 1986 DOI: 10.1016/S0040-4039(00)84634-1

InChI:InChI=1/C15H10O3/c16-11-6-7-14-12(8-11)13(17)9-15(18-14)10-4-2-1-3-5-10/h1-9,16H

6665-83-4 Relevant articles

Chromanone compound as well as preparation method and application thereof

-

Paragraph 0106-0111, (2021/04/26)

The invention discloses a chromanone com...

Design, synthesis, and biological evaluation of novel 4H-chromen-4-one derivatives as antituberculosis agents against multidrug-resistant tuberculosis

Fu, Lei,Liu, Yuke,Lu, Yu,Sheng, Li,Wang, Bin,Zhang, Dongfeng,Zhao, Hongyi,Zhao, Wenting

, (2020/01/28)

A series of 4H-chromen-4-one derivatives...

Nitrogen-containing flavonoid and their analogs with diverse B-ring in acetylcholinesterase and butyrylcholinesterase inhibition

Lu, Qiao-Qiao,Chen, Ya-Ming,Liu, Hao-Ran,Yan, Jian-Ye,Cui, Pei-Wu,Zhang, Qian-Fan,Gao, Xiao-Hui,Feng, Xing,Liu, Ying-Zi

, p. 1037 - 1047 (2020/08/06)

In this study, a series of new flavones ...

An efficient TBHP/TBAI-mediated protocol for the synthesis of 4H-chromen-4-ones from chroman-4-ones via oxidative C–C bond formation

Agisho, Habtamu Abebe,Hairat, Suboot,Zaki, Mehvash

, p. 599 - 603 (2020/05/04)

Abstract: A transition metal-free and ef...

6665-83-4 Process route

FLAVONE
525-82-6,66585-04-4

FLAVONE

6-hydroxyflavone
6665-83-4

6-hydroxyflavone

7-hydroxyflavone
6665-86-7,66585-10-2

7-hydroxyflavone

4'-hydroxyflavone
4143-63-9

4'-hydroxyflavone

Conditions
Conditions Yield
With cytochromes P450 in human liver microsomes; Kinetics; Enzymatic reaction;
6-hydroxyflavone
6665-83-4

6-hydroxyflavone

coumarin
91-64-5

coumarin

Conditions
Conditions Yield
59%

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