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484-18-4

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484-18-4 Usage

Description

1-(7-Hydroxy-5-methoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone is a complex chemical compound derived from the natural product chromone, featuring a chromenyl group and an ethanone group. It is also known as 7-hydroxy-5-methoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone and is found in various plants. 1-(7-Hydroxy-5-methoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone has potential pharmacological properties, with research indicating antioxidant and anti-inflammatory effects, and is being investigated for therapeutic use in various health conditions.

Uses

Used in Pharmaceutical Applications:
1-(7-Hydroxy-5-methoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone is used as a potential therapeutic agent for various health conditions due to its suggested antioxidant and anti-inflammatory properties. 1-(7-Hydroxy-5-methoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone is being investigated for its potential to treat a range of health issues, although further research is required to fully understand its mechanisms of action and applications.
Used in Research and Development:
In the field of scientific research, 1-(7-Hydroxy-5-methoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone serves as a subject of study to explore its pharmacological properties and potential applications in medicine. Its complex structure and natural origin make it an interesting candidate for the development of new drugs and therapies.
Used in the Nutraceutical Industry:
Given its antioxidant and anti-inflammatory properties, 1-(7-Hydroxy-5-methoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone may also be used as an additive or ingredient in the nutraceutical industry to enhance the health benefits of certain products, such as dietary supplements and functional foods. However, further research is needed to confirm its safety and efficacy in this context.

Check Digit Verification of cas no

The CAS Registry Mumber 484-18-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 484-18:
(5*4)+(4*8)+(3*4)+(2*1)+(1*8)=74
74 % 10 = 4
So 484-18-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H16O4/c1-8(15)12-10(16)7-11(17-4)9-5-6-14(2,3)18-13(9)12/h5-7,16H,1-4H3

484-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Alloevodionol

1.2 Other means of identification

Product number -
Other names alloevodinol

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:484-18-4 SDS

484-18-4Relevant articles and documents

DESIGN, SYNTHESIS AND FUNCTIONAL CHARACTERIZATION OF ROTTLERIN ANALOGS

-

Page/Page column 14, (2011/05/16)

A method of synthesizing rottlerin analogs is described. The synthesis methods described are the first known method of synthesizing rottlerin analogs from commercially-available materials to produce cost effective analogs. Rottlerin analog structures made by the synthesis methods and methods of use for treating a neurological or inflammatory response mediated by protein kinase C (PKC) are further described.

Convenient Synthesis of Alloevodione, Alloevodionol and Franklinone

Ahluwalia, V. K.,Jain, Anjula,Goyal, Madhuri

, p. 166 - 167 (2007/10/02)

3,4-Dihydro-6-hydroxy-5,7-dimethoxy-2,2-dimethyl-2H-1-benzopyran (5), obtained by nuclear prenylation of 2,6-dimethoxyquinol, on methylation followed by Friedel-Crafts acetylation gives 8-acetyl-3,4-dihydro-7-hydroxy-5,6-dimethoxy-2,2-dimethyl-2H-1-benzopyran (7).Dehydrogenation of 7 with DDQ followed by methylation affords alloevodione (9).Similar isoprenylation of 2,6-dihydroxy-4-methoxyacetophenone gives a mixture of dichroman (10) and the monochroman (11).Dehydrogenation of 10 and 11 furnishes franklinone (3) and alloevodionol (1) respectively.

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