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7-Chloro-2,3-dihydrobenzofuran-2-carboxylic acid is a chemical compound with a molecular formula C9H7ClO3. It is a derivative of benzofuran, featuring a carboxylic acid functional group and a chlorine atom. 7-Chloro-2,3-dihydrobenzofuran-2-carboxylic acid holds potential in medicinal chemistry and drug development due to its unique structure and possible biological activity.

26018-45-1

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26018-45-1 Usage

Uses

Used in Medicinal Chemistry:
7-Chloro-2,3-dihydrobenzofuran-2-carboxylic acid is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Drug Development:
7-Chloro-2,3-dihydrobenzofuran-2-carboxylic acid is used as a precursor in the development of new drugs. Its chemical properties and potential biological activity make it a valuable candidate for further research and exploration in the pharmaceutical industry.
Used in Research:
7-Chloro-2,3-dihydrobenzofuran-2-carboxylic acid is used as a subject of study in research to understand its physicochemical properties and potential uses in various fields. This knowledge can contribute to the advancement of science and the development of new applications for 7-Chloro-2,3-dihydrobenzofuran-2-carboxylic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 26018-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,1 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26018-45:
(7*2)+(6*6)+(5*0)+(4*1)+(3*8)+(2*4)+(1*5)=91
91 % 10 = 1
So 26018-45-1 is a valid CAS Registry Number.

26018-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Chloro-2,3-dihydro-1-benzofuran-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 7-Chloro-2,3-dihydrobenzofuran-2-carboxylic acid

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:26018-45-1 SDS

26018-45-1Downstream Products

26018-45-1Relevant academic research and scientific papers

α-Adrenoreceptor Reagents. 2. Effects of Modification of the 1,4-Benzodioxan Ring System on α-Adrenoreceptor Activity

Chapleo, Christopher B.,Myers, Peter L.,Butler, Richard C. M.,Davis, John A.,Doxey, John C.,et al.

, p. 570 - 576 (2007/10/02)

Modification of the 1,4-benzodioxan ring present in RX 781094 (1) has not previously been considered.This paper describes a number of analogues of this ring system, including compounds in which one of the oxygen atoms has been replaced by a methylene group and also those in which the ring size has been changed to give, for example, furan and thiophene derivatives.The dihydroxybenzofuranylimidazoline compound 7 is the only analogue possesing presynaptic antagonist potency and selectivity comparable to that of 1.In view of this result, a number of derivatives was prepared to determine the structure-activity relationships within this series.Many derivatives, as well as the parent compound 7, were found to possess presynaptic α2-adrenoreceptor antagonist and postsynaptic α1-adrenoreceptor partial agonist properties.Two of the selective presynaptic antagonists,13 and 14, possess greater potency and selectivity than that possessed by 1.The 5-chloro derivative 25 is twice as potent as 1 after oral administration but only about half as potent when given intravenously.

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