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29043-07-0

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29043-07-0 Usage

General Description

3',4',5',5,6,7-hexamethoxyflavone is a flavonoid compound that is derived from plants. It is a strong antioxidant and has shown potential in fighting inflammation, cancer, and other diseases. Research has also indicated that it may have anti-microbial and anti-fungal properties. Additionally, 3',4',5',5,6,7-hexamethoxyflavone has been studied for its potential to protect against cardiovascular diseases and support overall heart health. It is an interesting compound with a variety of potential health benefits, and further research is needed to fully understand its mechanisms and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 29043-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,4 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29043-07:
(7*2)+(6*9)+(5*0)+(4*4)+(3*3)+(2*0)+(1*7)=100
100 % 10 = 0
So 29043-07-0 is a valid CAS Registry Number.

29043-07-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,7-trimethoxy-2-(3,4,5-trimethoxyphenyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names 3',4',5,5',6,7-Hexamethoxyflavone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:29043-07-0 SDS

29043-07-0Relevant articles and documents

Highly oxygenated flavonoids from Murraya paniculata

Kinoshita, Takeshi,Firman, Kurnia

, p. 1207 - 1210 (1996)

Eight highly oxygenated flavones, including one new compound, were isolated from the leaves of an Indonesian medicinal plant, Murraya paniculata. Seven of them were identified as 5-hydroxy-6,7,8,3',4',5'- hexamethoxyflavone (gardenin A), 5,3'-dihydroxy-6,7,8,4',5'- pentamethoxyflavone (gardenin C), 6,7,8,4'-tetra-methoxy-5,3',5'- trihydroxyflavone (gardenin E), 5-hydroxy-6,7,8,3',4'-pentamethoxyflavone (5- O-desmethylnobiletin), 6,7,8,3',4',5'-hexamethoxyflavone, 5-hydroxy- 6,7,3',4',5'-pentamethoxyflavone (umhengerin), 5,3'-dihydroxy-6,7,4',5'- tetramethoxyflavone either by direct comparison with authentic samples or by comparing their melting points and spectroscopic data with those reported in the literature. The new compound was elucidated as 5,3',5'-trihydroxy- 6,7,4'-trimethoxyflavone on the basis of chemical and spectroscopic studies.

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

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

, (2021/08/12)

A series of 5,6,7-trimethoxyflavones 1a-1g and their derivatives 2a-2g, 3a-3d, 4 and 5, including the natural products 5,6,7-trimethoxy-4’-hydroxyflavone (1a), 5,6,7,3’,4’ -pentamethoxyflavone (sinensetin, 1 b), 5,6,7-trimethoxy-3’,4’-methyl enedioxy flavone (1c), 5,6,7,3’-tetramethoxy-4,5’-methylenedioxyflavone (1e), 5,6,7, 3’,4’,5’-hextamethoxyflavone (1 g), 5-hydroxy-3,4,2’,3’,4’-pentamethoxy chal-cone (2 b), 5,4’-dihydroxy-6,7-dimethoxy flavone (cirsimaritin, 3a) and 5-hydroxy-6,7,3’, 4’-tetramethoxyflavone (5-demethylsinensetin, 3 b), 3,5,6,7,3’,4’-hexamethoxyflavone (3-methoxysinensetin, 4) and 5’-hydroxy-3,6,7,3’,4’-pentamethoxyflavone (5) were synthesized. Their anti-proliferative activity in?vitro was evaluated against a panel of four human cancer cell lines (Aspc-1, HCT-116, HepG-2 and SUN-5) by the CTG assay. The results showed that most of the synthetic compounds exhibited moderate to high anti-proliferative activities. In particular, compound 3c possess IC50 (5.30 μM) values below 10 μM against Aspc-1 cells and are worthy of further investigation.

USE OF FLAVONE AND FLAVANONE DERIVATIVES IN PREPARATION OF SEDATIVE AND HYPNOTIC DRUGS

-

Paragraph 0223; 0238, (2015/07/22)

Disclosed is a use of flavones derivatives and flavanone derivatives in preparation of sedative and hypnotic drugs.

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