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CAS

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3-NITRO-PYRIDINE-2-CARBOXYLIC ACID, also known as 3-nitropyridine-2-carboxylic acid, is a chemical compound characterized by a pyridine ring with a carboxylic acid group and a nitro group attached to the 3rd and 2nd carbon atoms, respectively. It is a yellow crystalline solid with the molecular formula C6H4N2O4 and a molecular weight of 168.106 g/mol. 3-NITRO-PYRIDINE-2-CARBOXYLIC ACID is recognized for its role in the synthesis of various products and its potential biological activities and pharmacological properties.

59290-85-6

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59290-85-6 Usage

Uses

Used in Pharmaceutical Industry:
3-NITRO-PYRIDINE-2-CARBOXYLIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structure allows it to be a versatile building block in organic synthesis, facilitating the creation of a wide range of medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 3-NITRO-PYRIDINE-2-CARBOXYLIC ACID is utilized as a precursor in the production of agrochemicals, playing a crucial role in the development of pesticides and other agricultural chemicals that are essential for crop protection and enhancement of yield.
Used in Dye Industry:
3-NITRO-PYRIDINE-2-CARBOXYLIC ACID is used as a chemical intermediate in the synthesis of dyes, contributing to the coloration and staining processes in various applications, including textiles, plastics, and printing inks.
Used in Organic Synthesis:
As a key building block for organic synthesis, 3-NITRO-PYRIDINE-2-CARBOXYLIC ACID is employed in the production of various chemicals, highlighting its importance in the chemical industry for creating a multitude of chemical compounds with diverse applications.
Used in Research and Development:
3-NITRO-PYRIDINE-2-CARBOXYLIC ACID is also used in research and development settings for studying its potential biological activities and pharmacological properties, which may lead to the discovery of new therapeutic agents or applications in medicine and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 59290-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,9 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59290-85:
(7*5)+(6*9)+(5*2)+(4*9)+(3*0)+(2*8)+(1*5)=156
156 % 10 = 6
So 59290-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H4N2O4/c9-6(10)5-4(8(11)12)2-1-3-7-5/h1-3H,(H,9,10)

59290-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Nitropyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Nitropicolinic 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:59290-85-6 SDS

59290-85-6Relevant articles and documents

INHIBITORS OF FOCAL ADHESION KINASE

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Page/Page column 118, (2008/12/07)

The invention provides inhibitors of focal adhesion kinase, an enzyme involved in the attachment of the cytoskeleton of a cell to an extracellular matrix, which has been implicated in processes such as cell migration, cell proliferation, and cell survival. The inhibitors are derivatives of a 5-substituted 2,4-diaminopyridine wherein the substituents are as defined herein. The invention also provides a method of using the inhibitors in treatment of cancer, and methods of preparation of the inhibitors by use of coupling reactions.

PYRROLO[2,3-c]PYRIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF

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Page/Page column 22, (2010/10/20)

The present invention provides novel pyrrolo[2,3-c]pyridine derivatives or pharmaceutically acceptable salts thereof, processes for the preparation thereof, and compositions comprising the same. The pyrrolo[2,3-c]pyridine derivatives or pharmaceutically acceptable salts thereof of the present invention have excellent proton pump inhibition effects and possess the ability to attain a reversible proton pump inhibitory effect.

Fused ring 4-oxopyrimidine derivative

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Page/Page column 74, (2008/06/13)

The present invention provides a compound represented by formula (I) below, or a pharmaceutically acceptable salt thereof, which, having histamine H3 receptor antagonist or inverse agonist activity, is useful in the prophylaxis or therapy of metabolic diseases, circulatory diseases, or nervous system diseases. [where, for example, Ar is a divalent group formed by eliminating two hydrogen atoms from benzene, X1 is a nitrogen atom, sulfur atom or oxygen atom, R1 is a 5- to 6-membered heteroaryl group, Ring A is a 5- to 6-membered heteroaryl ring, R2 and R3 are amino groups or alkylamino groups, and X2 is represented by formula (II): (where R4 and R5 are lower alkyl groups, and n is an integer from 2 to 4).]

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