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2-(4-Hydroxyphenyl)-3-methyl-4H-chromen-4-one, also known as cirsimaritin, is a naturally occurring flavonoid compound found in various plants and herbs, such as Artemisia combrogi. It has been traditionally used in folk medicine and is known for its antioxidant, anti-inflammatory, and anti-cancer properties.

55456-75-2

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55456-75-2 Usage

Uses

Used in Cancer Therapy:
Cirsimaritin is used as a potential cancer therapy agent for its ability to inhibit the growth of cancer cells. It is being investigated for its potential role in cancer treatment.
Used in Neurodegenerative Disease Treatment:
Cirsimaritin is used as a neuroprotective agent for its potential in treating neurodegenerative diseases due to its neuroprotective effects.
Used in Autoimmune and Inflammatory Disease Treatment:
Cirsimaritin is used as an immunomodulatory agent for its potential in treating autoimmune and inflammatory diseases, as it has been linked to its ability to modulate the immune system.
Used in Pharmaceutical Industry:
Cirsimaritin is used as a pharmaceutical compound for its various therapeutic properties, including antioxidant, anti-inflammatory, and anti-cancer effects.
Used in Traditional Medicine:
Cirsimaritin is used in traditional medicine for its various health benefits, as it has been used in folk medicine for a long time.

Check Digit Verification of cas no

The CAS Registry Mumber 55456-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,5 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55456-75:
(7*5)+(6*5)+(5*4)+(4*5)+(3*6)+(2*7)+(1*5)=142
142 % 10 = 2
So 55456-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O3/c1-10-15(18)13-4-2-3-5-14(13)19-16(10)11-6-8-12(17)9-7-11/h2-9,17H,1H3

55456-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-hydroxyphenyl)-3-methylchromen-4-one

1.2 Other means of identification

Product number -
Other names 3-methyl-4'-hydroxyflavone

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:55456-75-2 SDS

55456-75-2Downstream Products

55456-75-2Relevant academic research and scientific papers

Synthesis of 3-methylflavones and their antioxidant and antibacterial activities

Jayashree, B. S.,Alam, Afroze,Vijay Kumar, D.,Nayak, Yogendra

, p. 1991 - 1996,6 (2020/07/30)

An attempt was made to synthesise newer 3-methylflavones with various substitution on the ring A and B of 2-phenylchromen-4-one. They were evaluated for antioxidant activity and antibacterial activity against the Gram-positive and Gram-negative bacteria.

Antioxidant and antibacterial activity of new 3-methylflavones

Jayashree,Alam, Afroze,Kumar, D. Vijay,Nayak, Yogendra

, p. 237 - 240 (2011/12/15)

Synthesis of new 3-methylflavones with various substitution on the ring A and B is being described. They were evaluated for antioxidant and antibacterial activity against Gram positive and Gram negative bacteria. Test compounds such as F-4,9,11,12 and 20

Selective C-monomethylation in 1-(2-hydroxyphenyl)-3-phenylpropane-1,3-diones and synthesis of 3-methylflavones

Makrandi, J K,Kumari, Vandna

, p. 1142 - 1144 (2007/10/02)

1-(2-Hydroxyphenyl)-3-phenylpropane-1,3-diones (Ia-f) on reaction with methyl iodide in benzene-aq. potassium carbonate biphase medium in the presence of tetra-n-butylammonium hydrogen sulphate as phase transfer catalyst give 2-methyl-1-(2-methoxyphenyl)-

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