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4-methylbenzofuran-2-carboxylic acid is an organic compound with the molecular formula C9H8O3. It is a derivative of benzofuran, which is a heterocyclic aromatic compound consisting of a benzene ring fused to a furan ring. The "4-methyl" prefix indicates that there is a methyl group (-CH3) attached to the benzene ring at the 4th position, while the "2-carboxylic acid" suffix signifies the presence of a carboxylic acid functional group (-COOH) at the 2nd position of the benzofuran ring. 4-methylbenzofuran-2-carboxylic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as a building block in the creation of more complex organic molecules. It is typically synthesized through chemical reactions involving benzofuran derivatives and can be further functionalized to yield a range of products with different properties and applications.

5670-24-6

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5670-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5670-24-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,7 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5670-24:
(6*5)+(5*6)+(4*7)+(3*0)+(2*2)+(1*4)=96
96 % 10 = 6
So 5670-24-6 is a valid CAS Registry Number.

5670-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-benzofuran-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Methylbenzofuran-2-carbonsaeure

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 -
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More Details:5670-24-6 SDS

5670-24-6Relevant 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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