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2-Benzofurancarboxylic acid, 5,6-dimethyl- is an organic compound with the chemical formula C10H10O3. It is a derivative of benzofuran, a heterocyclic aromatic compound consisting of a benzene ring fused to a furan ring. The 5,6-dimethyl substitution refers to the presence of two methyl groups (-CH3) attached to the benzofuran core, specifically at the 5th and 6th carbon atoms. 2-Benzofurancarboxylic acid, 5,6-dimethyl- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of other organic compounds. Its molecular structure and properties make it a valuable building block in the field of organic chemistry.

95835-74-8

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95835-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95835-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,3 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 95835-74:
(7*9)+(6*5)+(5*8)+(4*3)+(3*5)+(2*7)+(1*4)=178
178 % 10 = 8
So 95835-74-8 is a valid CAS Registry Number.

95835-74-8Downstream Products

95835-74-8Relevant 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paper describes a number of analogues of this ring system, including compounds in which one of the oxygen atoms has been replaced by a methylene group and also those in which the ring size has been changed to give, for example, furan and thiophene derivatives.The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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