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1-(5-Hydroxybenzofuran-4-yl)ethanone, also known as 5-hydroxy-4-benzofuranacetic acid ethyl ester, is an organic compound with the molecular formula C10H8O3. It is a derivative of benzofuran, a heterocyclic aromatic compound consisting of a benzene ring fused to a furan ring. The molecule features a hydroxyl group at the 5-position and an ethanone (keto) group at the 1-position, which is attached to the benzofuran core. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those containing the benzofuran scaffold. Due to its potential applications in drug development, it is an important compound in the field of medicinal chemistry.

1627-18-5

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1627-18-5 Usage

Molecular Structure

A derivative of benzofuran with a hydroxy group attached to the 5th position of the benzofuran ring

Antioxidant effects

Capable of neutralizing harmful free radicals in the body

Anti-inflammatory effects

May help reduce inflammation and swelling

Synthesis of organic compounds

Used as a building block for creating other complex organic molecules

Pharmaceutical synthesis

Utilized in the development of new drugs and medications

Research and Industrial Significance

Valued for its unique chemical structure and potential medicinal properties

Chemical Classification

Aromatic ketone

Solubility

Generally soluble in organic solvents like ethanol, methanol, and acetone

Stability

Relatively stable under normal conditions, but may decompose upon exposure to heat, light, or strong acids and bases

Check Digit Verification of cas no

The CAS Registry Mumber 1627-18-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1627-18:
(6*1)+(5*6)+(4*2)+(3*7)+(2*1)+(1*8)=75
75 % 10 = 5
So 1627-18-5 is a valid CAS Registry Number.

1627-18-5SDS

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-(5-hydroxy-1-benzofuran-4-yl)ethanone

1.2 Other means of identification

Product number -
Other names 5-Hydroxy-4-acetyl-benzofuran

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:1627-18-5 SDS

1627-18-5Downstream Products

1627-18-5Relevant academic research and scientific papers

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

A controlled synthesis of nature-mimicking benzofurans and their corresponding dimers

Dixit, Manish,Sharon, Ashoke,Maulik, Prakas R.,Goel, Atul

, p. 1497 - 1502 (2007/10/03)

Benzofurans functionalized with hydroxy and acetyl functionalities are not only the core structures found in a large number of biologically important natural products, but also the vital precursors for several naturally occurring furanoflavonoids. Numerou

STUDIES ON QUINONES. VI. ACID CATALIZED REARRANGEMENTS IN SOME 4-ACETYL-2,3-DIHYDROBENZOFURANS

Barrios, Luis,Ruiz, V. Manuel,Tapia, Ricardo,Valderrama, Jaime,Vega, Juan C.

, p. 187 - 190 (2007/10/02)

The reaction of 2-acetyl- and 5-acetyl-2-methoxy-1,4-benzoquinone (1a, 1c) with N-propenylpiperidine gave the corresponding 2,3-dihydrobenzofurans, 2b and 2c, containing the acetyl group at C-4.Acid treatment of these dihydrofurans rearranged to 8-methyl- and 2-methoxy-8-methyljuglone (4a, 4b).Juglone (4c) and 2,3-dihydrojuglone (6) were obtained in fair yields from 4-acetyl-2,5-dihydroxy-2,3-dihydrobenzofuran (2e).

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