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Sulfuretin

Basic information

  • Product Name:Sulfuretin
  • CasNo.:120-05-8
  • MF:C15H10 O5
  • MW:270.241

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:295°C
  • Packing:
  • Throughput:
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Product Details

CasNo: 120-05-8

MF: C15H10 O5

Manufacturers supply cost-effective and customizable Sulfuretin 120-05-8

  • Molecular Formula:C15H10O5
  • Molecular Weight:270.241
  • Vapor Pressure:2.79E-14mmHg at 25°C 
  • Melting Point:295°C 
  • Boiling Point:585 °C at 760 mmHg 
  • Flash Point:228.8 °C 
  • PSA:86.99000 
  • Density:1.597 g/cm3 
  • LogP:2.41960 

SULFURETIN(Cas 120-05-8) Usage

General Description

Sulfuretin is a natural organic compound that belongs to the flavonoid group of chemicals. It is found in various plants, including Sophora japonica and Rhus succedanea, and is responsible for the yellow and orange pigmentation in some flowers and fruits. Sulfuretin has been studied for its potential medicinal and therapeutic properties, including antioxidant, anti-inflammatory, and anti-cancer effects. It has also shown promising results in the treatment of skin conditions such as dermatitis and eczema. Additionally, sulfuretin has been investigated for its role in aiding insulin sensitivity and reducing the risk of diabetes. Research on sulfuretin is ongoing to further explore its potential applications in medicine and healthcare.

InChI:InChI=1/C15H10O5/c16-9-2-3-10-13(7-9)20-14(15(10)19)6-8-1-4-11(17)12(18)5-8/h1-7,16-18H/b14-6+

120-05-8 Relevant articles

Design, synthesis and biological activities of dihydroaurones

VENKATESWARLU, SOMEPALLI,MURTY, GANDROTU NARASIMHA,SATYANARAYANA, MEKA,SIDDAIAH, VIDAVALUR

, p. 1396 - 1402 (2021/06/09)

To widen aurones applicability in achrom...

Flavone inspired discovery of benzylidenebenzofuran-3(2H)-ones (aurones) as potent inhibitors of human protein kinase CK2

Bdzhola, V. G.,Bilokin, Y. V.,Borysenko, I. P.,Lukashov, S. S.,Protopopov, M. V.,Prykhod'ko, A. O.,Starosyla, S. A.,Vdovin, V. S.,Yarmoluk, S. M.

supporting information, (2020/07/21)

In this work, we describe the design, sy...

Aurones as new porcine pancreatic α-amylase inhibitors

Roshanzamir, Khashayar,Kashani-Amin, Elaheh,Ebrahim-Habibi, Azadeh,Navidpour, Latifeh

, p. 333 - 340 (2019/06/20)

Background: Aurones, (Z)-2-benzylidenebe...

"On water" synthesis of aurones: First synthesis of 4,5,3',4',5'-pentamethoxy-6-hydroxyaurone from Smilax riparia

Venkateswarlu, Somepalli,Murty, Gandrotu Narasimha,Satyanarayana, Meka

, p. 303 - 314 (2017/06/19)

A simple and green method for the synthe...

120-05-8 Process route

6-hydroxybenzofuran-3-one
6272-26-0

6-hydroxybenzofuran-3-one

3,4-dihydroxybenzaldehyde
139-85-5

3,4-dihydroxybenzaldehyde

sulfuretin
100433-06-5,120-05-8

sulfuretin

Conditions
Conditions Yield
With potassium hydroxide; In ethanol; water; for 3h; Reflux;
85%
In water; for 10h; Reflux; Green chemistry;
81%
In water; Reflux; Green chemistry;
81%
With hydrogenchloride; In ethanol; water; Reflux;
60%
With potassium hydroxide; In ethanol; water; at 80 ℃;
26%
With hydrogenchloride; In water; isopropyl alcohol; at 80 ℃; for 16h;
5%
With hydrogenchloride;
 
With hydrogenchloride; acetic acid;
 
With hydrogenchloride; ethanol;
 
4-hydroxy-3-ethoxybenzaldehyde
121-32-4

4-hydroxy-3-ethoxybenzaldehyde

6-hydroxybenzofuran-3-one
6272-26-0

6-hydroxybenzofuran-3-one

sulfuretin
100433-06-5,120-05-8

sulfuretin

Conditions
Conditions Yield
With potassium hydroxide; In methanol; water; for 3h; Reflux; Inert atmosphere;
44%

120-05-8 Upstream products

  • 6272-26-0
    6272-26-0

    6-hydroxybenzofuran-3-one

  • 139-85-5
    139-85-5

    3,4-dihydroxybenzaldehyde

  • 1360878-02-9
    1360878-02-9

    sulphuretin 3'-O-β-glucopyranoside

  • 36685-46-8
    36685-46-8

    (Z)-2-(3,4-dimethoxybenzylidene)-6-methoxybenzofuran-3(2H)-one

120-05-8 Downstream products

  • 5965-85-5
    5965-85-5

    6-acetoxy-2-((Z)-3,4-diacetoxy-benzylidene)-benzofuran-3-one

  • 1005324-89-9
    1005324-89-9

    2-(3,4-dihydroxybenzyl)-6-hydroxybenzofuran-3(2H)-one