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5-Methoxy-2-phenyl-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one, also known as Isopongaflavone, is a naturally occurring pyranoflavone compound found in Fordiae Cauliflorae Radix, a plant used in traditional Chinese medicine. It possesses unique structural features and potential therapeutic properties.

64125-33-3

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64125-33-3 Usage

Uses

Used in Neurological Applications:
Isopongaflavone is used as a therapeutic agent for the treatment of neurological diseases such as Alzheimer's, stroke, paralysis, and dementia. Its presence in Fordiae Cauliflorae Radix contributes to the plant's traditional use in Chinese medicine for addressing these conditions.
Used in Traditional Chinese Medicine:
Isopongaflavone is used as a key component in traditional Chinese medicine formulations, where it plays a role in the treatment of various neurological disorders. Its natural occurrence in Fordiae Cauliflorae Radix makes it a valuable resource for developing herbal remedies and treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 64125-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,2 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64125-33:
(7*6)+(6*4)+(5*1)+(4*2)+(3*5)+(2*3)+(1*3)=103
103 % 10 = 3
So 64125-33-3 is a valid CAS Registry Number.

64125-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name isopongaflavone

1.2 Other means of identification

Product number -
Other names 5-methoxy-8,8-dimethyl-2-phenyl-4H,8H-benzo[1,2-b:3,4-b

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:64125-33-3 SDS

64125-33-3Downstream Products

64125-33-3Relevant academic research and scientific papers

New synthetic approaches to naturally occurring and unnatural pyranoflavones

Xia, Likai,Rok Lee, Yong

, p. 644 - 650 (2013/05/09)

Total synthesis of biologically interesting natural and unnatural pyranoflavones has been accomplished starting from readily available 2,4-dihydroxyacetophenone or 2,4-dihydroxy-6-methoxyacetophenone in three steps, i.e., benzopyran formation, condensatio

Synthesis of isopongaflavone

Gissaub, M. Amzad,Tarafdar

, p. 540 - 543 (2007/10/03)

The synthesis of isopongaflavone1 9, a constituent of the seeds of Tephrosia bracteolata, is described. Phloroacetophenone 1 on treatment with chlorobutyne affords 2,6-dihydroxy-6′,6′-dimethyIpyrano[2′,3′: 4,3]acetophenone 2 which on methoxymethylation yields 2,6-di(methoxymethoxy)-6′, 6′-dimethylpyrano[2′,3′: 4,3]acetophenone 5. Alkaline condensation of 5 and benzaldehyde gives 2′, 6′-di(methoxymethoxy)-6″,6″-dimethylpyrano[2″, 3″ : 4′, 3′] chalcone 6. DDQ treatment of 2′, 6′-dihydroxy-6″,6″-dimethylpyrano[2″, 3″ : 4′, 3′] chalcone 7, obtained by the demethoxymethylation of 6, furnishes 5-hydroxy-6″,6″-dimethylpyrano[2″, 3″ : 4, 3]flavone 8 which on O-methylation gives 5-methoxy-6″,6″-dimethylpyrano[2″, 3″ : 4, 3]flavone 9.

A Facile Synthesis of Isopongaflavone, Atalantoflavone Dimethylether, Racemoflavone Dimethylether and their Analogues

Vijayalakshmi, C. S.,Prasad, K. J. Rajendra

, p. 1021 - 1025 (2007/10/02)

A convenient route to pyranoflavones (natural and synthetic) from acetyl hydroxy chroman via the corresponding analogues by the use of Claisen condensation in the key step is reported.Keywords: 2-Aryl-8,8-dimethyl-6,7-dihydro-4H,8H-benzodipy

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