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492440-03-6

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492440-03-6 Usage

Description

1-(4-(2,2-Diethoxyethoxy)-2-hydroxyphenyl)ethanone is a chemical compound with the molecular formula C14H20O5. It is a ketone derivative featuring a phenyl ring attached to an ethanone group, along with two diethoxyethoxy side chains and a hydroxyl group attached to the phenyl ring. 1-(4-(2,2-DIETHOXYETHOXY)-2-HYDROXYPHENYL)ETHANONE may serve as an intermediate in the synthesis of various organic compounds and could have potential applications in the pharmaceutical, cosmetic, and other industries. It is crucial to handle and use this compound with caution, adhering to proper safety protocols and guidelines for potentially hazardous chemicals.

Uses

Used in Pharmaceutical Industry:
1-(4-(2,2-Diethoxyethoxy)-2-hydroxyphenyl)ethanone is used as an intermediate in the synthesis of various pharmaceutical compounds for its potential applications in drug development.
Used in Cosmetic Industry:
1-(4-(2,2-Diethoxyethoxy)-2-hydroxyphenyl)ethanone is used as a component in the formulation of cosmetic products, potentially due to its chemical properties that may contribute to the product's efficacy or stability.
Used in Other Industries:
1-(4-(2,2-Diethoxyethoxy)-2-hydroxyphenyl)ethanone may also find applications in other industries where its unique chemical structure and properties can be utilized for specific purposes, such as in the development of new materials or chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 492440-03-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,2,4,4 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 492440-03:
(8*4)+(7*9)+(6*2)+(5*4)+(4*4)+(3*0)+(2*0)+(1*3)=146
146 % 10 = 6
So 492440-03-6 is a valid CAS Registry Number.

492440-03-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(2,2-diethoxyethoxy)-2-hydroxyphenyl]ethan-1-one

1.2 Other means of identification

Product number -
Other names 1-[4-(2,2-diethoxyethoxy)-2-hydroxyphenyl]ethanone

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:492440-03-6 SDS

492440-03-6Relevant articles and documents

TRICYCLIC COMPOUNDS ACTING ON CRBN PROTEINS

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Paragraph 0121-0122, (2021/07/17)

The present invention discloses a series of tricyclic compounds and use thereof in preparing a medicament for treating a disease related to CRBN protein. Specifically, the present invention discloses a derivative compound of formula (1) or a pharmaceutically acceptable salt thereof.

Synthesis of benzofuran scaffold-based potential PTP-1B inhibitors

Dixit, Manish,Tripathi, Brajendra K.,Tamrakar, Akhilesh K.,Srivastava, Arvind K.,Kumar, Brijesh,Goel, Atul

, p. 727 - 734 (2007/10/03)

Protein tyrosine phosphatase 1B (PTP-1B) is an enzyme that plays a critical role in down-regulating insulin signaling through dephosphorylation of the insulin receptor. Studies have shown that PTP-1B knockout mice showed increased insulin sensitivity in m

Isolation and synthesis of analgesic and anti-inflammatory compounds from Ochna squarrosa L.

Anuradha,Srinivas, Pullela V.,Ranga Rao,Manjulatha,Purohit, Muralidhar G.,Madhusudana Rao

, p. 6820 - 6826 (2007/10/03)

Two new furanoflavonoids (1, 2), one new chalcone dimer (3) along with six known compounds, chrysophanol, 5-O-methyl squarrosin, 5-methoxy furano[4″,5″,6,7]flavone, calodenone, lophirone A and lophirone H were isolated from the ethyl acetate-soluble fraction of methanol extract of root bark of Ochna squarrosa. Chrysophanol, calodenone, lophirone A and lophirone H were isolated from this plant for the first time. The structures of all the isolated compounds were confirmed by 1D and 2D spectroscopic data. These compounds were tested for analgesic and anti-inflammatory activity. All the new compounds showed good analgesic and anti-inflammatory activity. A simple and facile method for the cleavage of benzyl ethers using I2 in trigol is also reported.

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