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3-Pyridinecarboxylic acid, 2,6-diamino (9CI), also known as 2,6-diaminonicotinic acid, is a chemical compound with the molecular formula C7H8N4O2. It features a pyridine ring with two amino groups attached to the 2 and 6 positions, making it a versatile building block for the synthesis of various pharmaceuticals and agrochemicals. 3-Pyridinecarboxylicacid,2,6-diamino-(9CI) also has potential applications in material science and organic synthesis, and its biological activities are being researched for potential medicinal properties.

175155-53-0

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175155-53-0 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
3-Pyridinecarboxylic acid, 2,6-diamino (9CI) is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic and pesticidal properties.
Used in Material Science:
In the field of material science, 3-Pyridinecarboxylic acid, 2,6-diamino (9CI) is utilized for the development of new materials with specific properties, such as conductivity or reactivity, due to its versatile chemical structure.
Used in Organic Synthesis:
3-Pyridinecarboxylic acid, 2,6-diamino (9CI) serves as an important intermediate in organic synthesis, enabling the creation of a wide range of organic compounds for various applications.
Used in Medicinal Research:
3-Pyridinecarboxylic acid, 2,6-diamino (9CI) is the subject of research for its potential medicinal properties, as it may possess biological activities that could be harnessed for the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 175155-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,5 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 175155-53:
(8*1)+(7*7)+(6*5)+(5*1)+(4*5)+(3*5)+(2*5)+(1*3)=140
140 % 10 = 0
So 175155-53-0 is a valid CAS Registry Number.

175155-53-0SDS

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 2,6-diaminopyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,6-DIAMINONICOTINIC 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:175155-53-0 SDS

175155-53-0Relevant academic research and scientific papers

NOVEL ANTIMALARIAL AGENT CONTAINING HETEROCYCLIC COMPOUND

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Paragraph 0057; 0071; 0074, (2021/07/31)

Disclosed herein are diaminopyridine compounds or pharmaceutically acceptable salts thereof having antimalarial activation effect.

PYRIDINE DERIVATIVE SUBSTITUTED BY HETEROARYL RING, AND ANTIFUNGAL AGENT COMPRISING THE SAME

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Page/Page column 73, (2009/06/27)

The present invention provides an antifungal agent that has excellent antifungal action, and is also excellent in terms of its properties, safety, and metabolic stability. The present invention discloses a compound represented by the following formula I or a salt thereof, and an antifungal agent comprising the compound or the salt: wherein R1 represents a hydrogen atom, a halogen atom, an amino group, a C1-6 alkyl group, a C1-6 alkoxy group, or a C1-6-alkoxy-C1-6-alkyl group; R2 represents a hydrogen atom or an amino group; X, Y, Z, and W independently represent a nitrogen atom, an oxygen atom, a sulfur atom, or -CH-, provided that at least two among X, Y, and W are nitrogen atoms; the ring A represents a 5- or 6-membered heteroaryl ring or a benzene ring; Q represents a methylene group, an oxygen atom, -CH2O-, -OCH2-, -NH-, -NHCH2-, or -CH2NH-; and R3 represents a C1-6 alkyl group, a C3-8 cycloalkyl group, a C6-10 aryl group, or a 5- or 6-membered heteroaryl group, each of which may have one or two substituents.

NOVEL ANTIMALARIA AGENT CONTAINING HETEROCYCLIC COMPOUND

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Page/Page column 44, (2008/06/13)

Disclosed is an antimalarial agent containing a compound represented by the formula: [wherein A1 represents a 3-pyridyl group that may have a substituent, a 6-quinolyl group that may have a substituent, or the like; X1 represents a group represented by the formula -C(=O)-NH- or the like; E represents a furyl group, a thienyl group or a phenyl group; with the proviso that A1 may have one to three substituents, and E has one of two substituents] or a salt thereof or hydrates thereof.

ANTIFUNGAL AGENT CONTAINING PYRIDINE DERIVATIVE

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Page/Page column 35, (2008/06/13)

The present invention provides an antifungal agent that has superior antifungal action and is also superior in terms of physical properties, safety and metabolic stability. The present invention discloses a compound represented by the formula (I): (wherein X represents an oxygen atom, a sulfur atom or -NH-, R1 represents a hydrogen atom, a halogen atom, a cyano group, an amino group or a substituent, and R2 and R3 independently represent a hydrogen atom, a halogen atom, a hydroxyl group or a substituent, except for a case in which R2 and R3 are both hydrogen atoms), and an antifungal agent containing the above compound.

NOVEL ANTIFUNGAL AGENT COMPRISING HETEROCYCLIC COMPOUND

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Page/Page column 52, (2010/11/08)

The present invention provides an antifungal agent represented by the formula: [wherein A1 represents a 3-pyridyl group which may have a substituent, a quinolyl group which may have a substituent, or the like; X1 represents a group represented by the formula -NH-C(=O)-, a group represented by the formula -C(=O)-NH-, or the like; E represents a furyl group, a thienyl group, a pyrrolyl group, a phenyl group, a pyridyl group, a tetrazolyl group, a thiazolyl group or a pyrazolyl group; with the proviso that A1 may have 1 to 3 substituents, and E has one or two substituents].

Chichibabin aminations of pyridine bases

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, (2008/06/13)

Improved Chichibabin aminations of pyridine bases are described which are conducted under a pressurized gas phase containing ammonia and in the presence of a selected additive which increases the reaction rate, and also in preferred processes favorably alters the isomer ratios and product yields from the aminations while benefiting product workup and recovery as well.

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