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7622-53-9

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7622-53-9 Usage

General Description

5-Deoxycajanin is a chemical compound belonging to the cajanin family, derived from the Cajanus cajan (pigeon pea) plant. It is a flavonoid known for its biological activities, including antioxidant, anti-inflammatory, and anti-cancer properties. Studies have shown that 5-deoxycajanin has the potential to inhibit the growth of breast cancer cells and induce apoptosis. It has also been found to have neuroprotective effects, making it a potential candidate for the treatment of neurodegenerative diseases. Additionally, 5-deoxycajanin has been reported to possess anti-diabetic properties, and may be useful in managing diabetes and related complications. Overall, 5-deoxycajanin shows promise as a natural compound with therapeutic potential for various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 7622-53-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7622-53:
(6*7)+(5*6)+(4*2)+(3*2)+(2*5)+(1*3)=99
99 % 10 = 9
So 7622-53-9 is a valid CAS Registry Number.

7622-53-9SDS

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 3-(2,4-dihydroxyphenyl)-7-methoxychromen-4-one

1.2 Other means of identification

Product number -
Other names 2',4'-dihydroxy-7-methoxyisoflavone

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:7622-53-9 SDS

7622-53-9Relevant articles and documents

Insect antifeedants, pterocarpans and pterocarpol, in heartwood of Pterocarpus macrocarpus Kruz

Morimoto, Masanori,Fukumoto, Hiromi,Hiratani, Masaru,Chavasiri, Warinthorn,Komai, Koichiro

, p. 1864 - 1868 (2006)

The insect antifeedant activities of pterocarpans and a sesquiterpene alcohol from the dichloromethane extract of Pterocarpus macrocarpus Kruz. (Leguminosae) were evaluated against the common cutworm, Spodoptera litura F. (Noctuidae), and the subterranean

A facile synthesis of biogenetic precursor, puerarone, isolated from Pueraria sp

Khan,Kapil

, p. 1007 - 1009 (2007/10/03)

Puerarone was synthesized using chalcone oxidation with thallium (III) trinitrate and chromenation of the resulting isoflavone using 3-hydroxyisovaleraldehyde dimethylacetal. The key demethylation step was achieved with boron tribromide.

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