2306-27-6

  • Product Name:SINENSETIN
  • Molecular Formula:C20H20O7
  • Molecular Weight:372.375
  • Appearance:pale creamy yellow powder
Inquiry

Product Details

pd_meltingpoint:174-176°C

Appearance:pale creamy yellow powder

Purity:99%

Factory supply SINENSETIN 2306-27-6 with sufficient production capacity

  • Molecular Formula:C20H20O7
  • Molecular Weight:372.375
  • Appearance/Colour:pale creamy yellow powder 
  • Vapor Pressure:4.73E-12mmHg at 25°C 
  • Melting Point:174-176°C 
  • Refractive Index:1.565 
  • Boiling Point:547.76 °C at 760 mmHg 
  • Flash Point:240.561 °C 
  • PSA:76.36000 
  • Density:1.244 g/cm3 
  • LogP:3.50300 

SINENSETIN(Cas 2306-27-6) Usage

Biochem/physiol Actions

Sinensetin is a citris flavonoid with anti-inflammatory and anti-proliferative activity. It has also been shown to enhance adipogenesis and lipolysis.

Definition

ChEBI: A pentamethoxyflavone that is flavone substituted by methoxy groups at positions 5, 6, 7, 3' and 4' respectively.

General Description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

InChI:InChI=1/C20H20O7/c1-22-13-7-6-11(8-15(13)23-2)14-9-12(21)18-16(27-14)10-17(24-3)19(25-4)20(18)26-5/h6-10H,1-5H3

2306-27-6 Relevant articles

5,6-DIMETHOXY-7,3',4',-TRIHYDROXYFLAVONE FROM ANISOMELES OVATA

Rao, L. Jagan Mohan,Kumari, G. N. Krishna,Rao, N. S. Prakasa

, p. 1522 (1983)

5,6-Dimethoxy-7,3',4'-trihydroxyflavone ...

-

Morita et al.

, p. 421,423 (1973)

-

Synthesis and anti-proliferative activities of 5,6,7-trimethoxyflavones and their derivatives

Li, Wei,Liu, Kexiong,Su, Liang,Wang, Qiuan

supporting information, (2021/08/12)

A series of 5,6,7-trimethoxyflavones 1a-...

Nobiletin derivative or pharmaceutically acceptable salt thereof as well as preparation method and application thereof

-

Paragraph 0097; 0102-0104, (2019/12/09)

The invention discloses a nobiletin deri...

Use of flavone and flavanone derivatives in preparation of sedative and hypnotic drugs

-

Page/Page column 48; 49; 50; 51, (2017/07/01)

Disclosed is a use of flavones derivativ...

Semi-synthesis and NMR spectral assignments of flavonoid and chalcone derivatives

Kumar, Rohitesh,Lu, Yuting,Elliott, Alysha G.,Kavanagh, Angela M.,Cooper, Matthew A.,Davis, Rohan A.

, p. 880 - 886 (2016/10/25)

Previous investigations of the aerial pa...

2306-27-6 Process route

3,4-dimethoxybenzoic acid chloride
3535-37-3

3,4-dimethoxybenzoic acid chloride

Eudesmic acid
118-41-2

Eudesmic acid

sinensetin
2306-27-6,27181-91-5

sinensetin

Conditions
Conditions Yield
3,4-dimethoxybenzoic acid chloride; Eudesmic acid; With triethylamine; In dichloromethane; at 0 - 20 ℃; for 2h;
With trimethylsilyl trifluoromethanesulfonate; triethylamine; In dichloromethane; at 95 ℃; for 2h;
81%
2'-hydroxy-3,4,4',5',6'-pentamethoxychalcone
65602-54-2

2'-hydroxy-3,4,4',5',6'-pentamethoxychalcone

sinensetin
2306-27-6,27181-91-5

sinensetin

Conditions
Conditions Yield
With sulfuric acid; In dimethyl sulfoxide; Heating;
76%

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2306-27-6 Downstream products

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