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3-AMINO-2-HYDROXY-4-PICOLINE, also known as 3-amino-1-hydroxy-2-methylpyridin-4(1H)-one, is a heterocyclic chemical compound belonging to the picoline derivatives. It features a pyridine ring with a hydroxy and amino group attached, offering unique structural features that make it a versatile building block in various chemical applications.

33252-54-9

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33252-54-9 Usage

Uses

Used in Pharmaceutical Synthesis:
3-AMINO-2-HYDROXY-4-PICOLINE is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and medicinal compounds. Its unique structure allows for the creation of diverse organic molecules with potential therapeutic properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, 3-AMINO-2-HYDROXY-4-PICOLINE is utilized as a key component in the synthesis of various agrochemicals, such as pesticides and herbicides. Its ability to form complex organic molecules makes it valuable in developing effective and targeted agricultural solutions.
Used in Fine Chemicals Synthesis:
3-AMINO-2-HYDROXY-4-PICOLINE is employed as a building block in the synthesis of fine chemicals, which are high-purity chemicals used in various industries, including cosmetics, fragrances, and flavorings. Its versatility in forming complex structures is essential for creating specialized chemical products.
Used in Metal Extraction and Separation Processes:
Leveraging its chelating properties, 3-AMINO-2-HYDROXY-4-PICOLINE is used in metal extraction and separation processes. It forms stable complexes with metal ions, facilitating their extraction and separation from other elements, which is crucial in various industrial applications.
Used in Catalysis and Coordination Chemistry:
Due to its unique structural features, 3-AMINO-2-HYDROXY-4-PICOLINE has potential applications in the field of catalysis and coordination chemistry. It can act as a catalyst or ligand in various chemical reactions, enhancing reaction rates and selectivity, and contributing to the development of new catalytic systems.

Check Digit Verification of cas no

The CAS Registry Mumber 33252-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,5 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33252-54:
(7*3)+(6*3)+(5*2)+(4*5)+(3*2)+(2*5)+(1*4)=89
89 % 10 = 9
So 33252-54-9 is a valid CAS Registry Number.
InChI:InChI=1S/C6H8N2O/c1-4-2-3-8-6(9)5(4)7/h2-3H,7H2,1H3,(H,8,9)

33252-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-4-methyl-1H-pyridin-2-one

1.2 Other means of identification

Product number -
Other names 3-Amino-4-methylpyridin-2-ol

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:33252-54-9 SDS

33252-54-9Relevant academic research and scientific papers

Identification of the First Synthetic Allosteric Modulator of the CB2 Receptors and Evidence of Its Efficacy for Neuropathic Pain Relief

Gado, Francesca,Di Cesare Mannelli, Lorenzo,Lucarini, Elena,Bertini, Simone,Cappelli, Elena,Digiacomo, Maria,Stevenson, Lesley A.,Macchia, Marco,Tuccinardi, Tiziano,Ghelardini, Carla,Pertwee, Roger G.,Manera, Clementina

, p. 276 - 287 (2018/07/21)

The direct activation of cannabinoid receptors (CBRs) results in several beneficial effects; therefore several CBRs ligands have been synthesized and tested in vitro and in vivo. However, none of them reached an advanced phase of clinical development due

FUSED HETEROCYCLIC DERIVATIVES AS PPAR MODULATORS

-

Page 213-214, (2008/06/13)

The present invention is directed to compounds represented by the following structural formula, Formula I: wherein (a) X is selected from the group consisting of a single bond, O, S. S(O)2 and N; (b) U is an aliphatic linker; (c) Y is selected from the group consisting of C, O, S, NH and a single bond; (d) E is C(R3) (R4)A or A and wherein (i) A is selected from the group consisting of carboxyl, tetrazole, C1-C6 alkylnitrile, carboxamidek, sulfonamide and acylsulfonamide; (e) B is selected from the group consisting of S, O, C, and N; (f) Z is selected from the group consisting of N and C; with the proviso that when B is C then Z is N.

Antipicornaviral compounds and compositions, their pharmaceutical uses, and materials for their synthesis

-

, (2008/06/13)

Compounds of the formula: where the formula variables are as defined herein, are disclosed that advantageously inhibit or block the biological activity of the picornaviral 3C protease. Also disclosed are compounds of the formula: where the formula variables are as defined herein that advantageously inhibit or block the biological activity of the picornaviral 3C protease. These compounds, as well as pharmaceutical compositions containing these compounds, are useful for treating patients or hosts infected with one or more picornaviruses, such as rhinovirus 3C proteases. Intermediates and synthetic methods for preparing such compounds are also described.

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