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7-Hydroxy-4-methoxymethylcoumarin, also known as HMMC, is a naturally occurring chemical compound belonging to the coumarin family, found in various plants. It is recognized for its antioxidant and anti-inflammatory properties, and has demonstrated potential therapeutic effects for a range of health conditions, including cancer, diabetes, and cardiovascular diseases. HMMC also exhibits antimicrobial properties, making it a candidate for use as a natural food preservative, and has significant anti-aging and skin-protective properties, which are valuable in cosmetics and skincare products.

157101-77-4

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157101-77-4 Usage

Uses

Used in Pharmaceutical Applications:
7-Hydroxy-4-methoxymethylcoumarin is used as a therapeutic agent for various health conditions due to its potential effects on cancer, diabetes, and cardiovascular diseases. Its antioxidant and anti-inflammatory properties contribute to its medicinal value.
Used in Food Preservation:
In the food industry, 7-Hydroxy-4-methoxymethylcoumarin is used as a natural preservative for its antimicrobial properties, helping to extend the shelf life of food products.
Used in Cosmetics and Skincare:
7-Hydroxy-4-methoxymethylcoumarin is used as an ingredient in cosmetics and skincare products for its anti-aging and skin-protective properties, enhancing the health and appearance of the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 157101-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,1,0 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 157101-77:
(8*1)+(7*5)+(6*7)+(5*1)+(4*0)+(3*1)+(2*7)+(1*7)=114
114 % 10 = 4
So 157101-77-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O4/c1-14-6-7-4-11(13)15-10-5-8(12)2-3-9(7)10/h2-5,12H,6H2,1H3

157101-77-4 Well-known Company Product Price

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  • Alfa Aesar

  • (A18562)  7-Hydroxy-4-(methoxymethyl)coumarin, 98%   

  • 157101-77-4

  • 1g

  • 790.0CNY

  • Detail
  • Alfa Aesar

  • (A18562)  7-Hydroxy-4-(methoxymethyl)coumarin, 98%   

  • 157101-77-4

  • 5g

  • 2926.0CNY

  • Detail

157101-77-4SDS

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 7-hydroxy-4-(methoxymethyl)chromen-2-one

1.2 Other means of identification

Product number -
Other names -

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:157101-77-4 SDS

157101-77-4Downstream Products

157101-77-4Relevant academic research and scientific papers

Cholinium ionic liquids as cheap and reusable catalysts for the synthesis of coumarins via Pechmann reaction under solvent-free conditions

Zhang, Yuehua,Zhu, Anlian,Li, Qianqian,Li, Lingjun,Zhao, Yang,Wang, Jianji

, p. 22946 - 22950 (2014)

A cheap cholinium ionic liquid N,N′-dimethylaminoethanol hydrosulfate ([N112OH][HSO4]) was found to be an efficient and reusable catalyst for the Pechmann condensation under solvent-free conditions. The coumarin products can be simply separated and the ionic liquid catalyst can be recycled and reused for at least six runs without noticeable decrease in the catalytic activity. The UV-vis studies suggested that the increase of the acidity and the introduction of a hydroxyl group to the cation benefit the existence of the keto tautomer of ethyl acetoacetate, which then leads to the excellent performance of [N112OH][HSO4].

Coumarins as novel 17β-hydroxysteroid dehydrogenase type 3 inhibitors for potential treatment of prostate cancer

Harada, Koichiro,Kubo, Hideki,Tomigahara, Yoshitaka,Nishioka, Kazuhiko,Takahashi, Junya,Momose, Mio,Inoue, Shinichi,Kojima, Atsuyuki

scheme or table, p. 272 - 275 (2010/04/06)

The synthesis and SAR studies of 3- and 4-substituted 7-hydroxycoumarins as novel 17β-HSD3 inhibitors are discussed. The most potent compounds from this series exhibited low nanomolar inhibitory activity with acceptable selectivity versus other 17β-HSD isoenzymes and nuclear receptors.

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