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1,3-Benzenedicarboxylic acid, 2-hydroxy-5-nitro-, dimethyl ester is a complex organic compound with the chemical formula C10H9NO8. It is derived from 1,3-benzenedicarboxylic acid, which is a dicarboxylic acid with two carboxylic acid groups attached to a benzene ring. In this specific compound, the 2-position on the benzene ring is substituted with a hydroxyl group (-OH), and the 5-position is substituted with a nitro group (-NO2). The dimethyl ester functional group is formed by the esterification of the two carboxylic acid groups with methanol, resulting in two methyl ester groups (-COOCH3). 1,3-Benzenedicarboxylic acid, 2-hydroxy-5-nitro-, dimethyl ester is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, and it is characterized by its unique chemical structure and properties.

67294-54-6

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67294-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67294-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,9 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67294-54:
(7*6)+(6*7)+(5*2)+(4*9)+(3*4)+(2*5)+(1*4)=156
156 % 10 = 6
So 67294-54-6 is a valid CAS Registry Number.

67294-54-6Relevant academic research and scientific papers

BENZAMIDINE DERIVATIVES

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, (2008/06/13)

Benzamidine derivatives of formula (I) or pharmaceutically acceptable salts thereof exhibit excellent inhibitory activity against factor Xa and are useful for treating or preventing blood coagulation disorders: wherein R 1represents a hydrogen atom, a halogen atom, an alkyl group or a hydroxyl group; R 2represents a hydrogen atom, a halogen atom or an alkyl group, R 3represents a hydrogen atom, an optionally substituted alkyl group, an aralkyl group, an optionally substituted alkanoyl group or an optionally substituted alkylsulfonyl group, R 4and R 5 are the same as or different from each other and each represent a hydrogen atom, a halogen atom, an optionally substituted alkyl group, an alkoxy group, a carboxyl group, an alkoxycarbonyl group or an optionally substituted carbamoyl group, and R 6represents a substituted pyrrolidine group or substituted piperidine group.

Syntheses and UV-visible spectroscopic properties of two new hydrophilic 2,6-di(carbamoyl)-substituted solvatochromic pyridinium N-phenolate betaine dyes

Reichardt, Christian,Roechling, Andreas,Schaefer, Gerhard

, p. 682 - 690 (2007/10/03)

Synthesis and negative solvatochromism of two 2,6-di(carbamoyl) -substituted pyridinium N-phenolate betaines dyes were investigated. The exceptionally large negative solvatochromism of the standard betaine dye was used to establish a UV-Vis spectroscopically derived scale of solvent polarity. It was found that the primary indicator dye was sufficiently soluble in most organic solvents.

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