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1-tert-butyl-3-methyl 5-nitro-indole-1,3-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1058740-09-2

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1058740-09-2 Usage

Chemical class

Indole derivatives

Explanation

1-tert-butyl-3-methyl 5-nitro-indole-1,3-dicarboxylate belongs to the class of indole derivatives, which are compounds derived from the indole ring structure.

Explanation

A tert-butyl group (C4H9) is attached to the indole ring, which is a saturated hydrocarbon group and can influence the compound's stability and reactivity.

Explanation

A methyl group (CH3) is also attached to the indole ring, which is a small alkyl group consisting of one carbon atom and three hydrogen atoms.

Explanation

A nitro group (-NO2) is attached to the indole ring at the 5-position, which can enhance the compound's reactivity and contribute to its potential applications in various fields.

Explanation

Two carboxylate groups (-COO^-) are attached to the 1 and 3 positions of the indole ring, which can participate in various chemical reactions and contribute to the compound's biological activity.

Explanation

Indole derivatives are known to exhibit a wide range of biological activities, such as anticancer, antimicrobial, and anti-inflammatory properties. 1-tert-butyl-3-methyl 5-nitro-indole-1,3-dicarboxylate may have potential applications in the pharmaceutical industry due to these properties.

Explanation

The presence of the nitro group in 1-tert-butyl-3-methyl 5-nitro-indole-1,3-dicarboxylate might contribute to its reactivity and potential use as a synthetic intermediate in organic chemistry, allowing for the synthesis of other related compounds.

Explanation

Further research and study are necessary to fully elucidate the properties and potential uses of 1-tert-butyl-3-methyl 5-nitro-indole-1,3-dicarboxylate, as its full potential and applications are not yet fully understood.

Check Digit Verification of cas no

The CAS Registry Mumber 1058740-09-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,8,7,4 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1058740-09:
(9*1)+(8*0)+(7*5)+(6*8)+(5*7)+(4*4)+(3*0)+(2*0)+(1*9)=152
152 % 10 = 2
So 1058740-09-2 is a valid CAS Registry Number.

1058740-09-2Downstream Products

1058740-09-2Relevant academic research and scientific papers

NEW SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS

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Page/Page column 136, (2008/12/07)

The present invention relates to substituted arylsulphonylglycines of general formula (I) wherein R, X, Y and Z are defined as in claim 1, the tautomers, enantiomers, diastereomers, mixtures thereof and salts thereof, which have valuable pharmacological properties, particularly the suppression of the interaction of glycogen phosphorylase a with the GL subunit of glycogen-associated protein phosphatase 1 (PP1 ), and their use as pharmaceutical compositions.

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