Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyran compounds >  SCOPARONE

SCOPARONE

Basic information Safety Supplier Related

SCOPARONE Basic information

Product Name:
SCOPARONE
Synonyms:
  • Scoparone 120-08-1
  • 6,7-dihydroxy-3,4-dimethyl-1-benzopyran-2-one
  • 6,7-dimethoxy-coumari
  • 6,7-Dimethoxycoumarine
  • aesculetindimethylether
  • escoparone
  • scoparon
  • 6,7-DIMETHOXY-CHROMEN-2-ONE
CAS:
120-08-1
MF:
C11H10O4
MW:
206.19
EINECS:
204-369-0
Product Categories:
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
  • Inhibitors
  • Coumarins
  • API intermediates
Mol File:
120-08-1.mol
More
Less

SCOPARONE Chemical Properties

Melting point:
143-145 °C (lit.)
Boiling point:
265.04°C (rough estimate)
Density 
1.0858 (rough estimate)
refractive index 
1.4389 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
>8.4mg/mL in DMSO
form 
Powder
color 
Light yellow to yellow
Merck 
13,8479
LogP
1.331 (est)
CAS DataBase Reference
120-08-1(CAS DataBase Reference)
NIST Chemistry Reference
2H-1-benzopyran-2-one, 6,7-dimethoxy-(120-08-1)
More
Less

Safety Information

Hazard Codes 
Xn
Risk Statements 
23/24/25-36-22
Safety Statements 
27/28-36/37/39-45-26
RIDADR 
2811
WGK Germany 
3
RTECS 
GN6550000
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
29322090
More
Less

SCOPARONE Usage And Synthesis

Uses

Scoparone-13C2D6 is a by-product in the synthesis of Scopoletin-13C,d3 (S200502). Scopoletin-13C,d3, is the labeled analogue of Scopoletin (S200500), used for cosmetics, topical formulations, and foods. Scoparone-13C2D6 is also the labeled form of Scoparone (S199980), which regulates the expression of Th1/Th2 cytokines and IgE and is effective in treating allergic rhinitis.

Definition

ChEBI: Scoparone is a member of the class of coumarins that is esculetin in which the two hydroxy groups at positions 6 and 7 are replaced by methoxy groups. It is a major constituent of the Chinese herbal medicine Yin Chen Hao, and exhibits a variety of pharmacological activities such as anti-inflammatory, anti-allergic, and anti-tumor activities. It has a role as a plant metabolite, an anti-inflammatory agent, an antilipemic drug, an immunosuppressive agent, an antihypertensive agent and an anti-allergic agent. It is a member of coumarins and an aromatic ether. It is functionally related to an esculetin.

Synthesis Reference(s)

Synthesis, p. 1026, 1986 DOI: 10.1055/s-1986-31859

General Description

6,7-Dimethoxycoumarin inhibits the in vitro growth of Phytophthora citrophthora, Verticillium dahliae, Penicillium digitatum, P. italicum, Colletotrichum gloeosporioides, Diplodia natalensis and Hendersonula toruloidea. Determination and pharmacokinetic study of 6,7-dimethoxycoumarin in rat plasma after intragastric administration of different decoctions of Yinchenhao Tang by reversed-phase HPLC method with UV detection has been reported.

Safety Profile

Poison by ingestion and intraperitoneal routes. Experimental reproductive effects. An anthypertensive agent. When heated to decomposition it emits acrid smoke and irritating fumes.

SCOPARONE Preparation Products And Raw materials

Raw materials

SCOPARONESupplier

Shanghai Moqi Biological Technology Co., LTD Gold
Tel
021-38218169 13341702378
Email
190129269@qq.com
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Chembest Research Laboratories Limited
Tel
+86-21-20908456
Email
sales@BioChemBest.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Email
sales@capotchem.com