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Umuhengerin is a naturally occurring chemical compound found in the plant species Uvaria umbellata, which is native to Africa. It belongs to the family of alkaloids and is known for its potential bioactivity, particularly as an antifeedant, which means it can deter certain insects from feeding on plants. Research on umuhengerin and its derivatives is ongoing to explore their potential applications in agriculture and possibly in医药领域 as well. The compound's structure and properties are of interest to scientists due to its unique chemical features and the possibility of it having a range of biological effects.

29215-55-2

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29215-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29215-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,1 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29215-55:
(7*2)+(6*9)+(5*2)+(4*1)+(3*5)+(2*5)+(1*5)=112
112 % 10 = 2
So 29215-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H20O8/c1-23-14-6-10(7-15(24-2)19(14)26-4)12-8-11(21)17-13(28-12)9-16(25-3)20(27-5)18(17)22/h6-9,22H,1-5H3

29215-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

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

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:29215-55-2 SDS

29215-55-2Relevant academic research and scientific papers

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.

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