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5-tert-butylpyridine-2-carboxylic acid, a chemical compound with the molecular formula C14H19NO2, is a derivative of pyridine featuring a tert-butyl group attached to the nitrogen atom. This versatile compound has garnered attention for its potential applications across various industries, including pharmaceuticals, materials science, and medicine.

1005785-85-2

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1005785-85-2 Usage

Uses

Used in Pharmaceutical Industry:
5-tert-butylpyridine-2-carboxylic acid is utilized as a building block in organic synthesis for the production of various drugs and pharmaceutical intermediates. Its unique structure allows for the creation of novel compounds with potential therapeutic effects.
Used in Corrosion Inhibition:
5-tert-butylpyridine-2-carboxylic acid is studied for its potential use as a corrosion inhibitor, offering a means to protect materials from degradation in various industrial applications, thereby extending their service life and reducing maintenance costs.
Used in Antimicrobial Materials Development:
5-terbutylpieolinic acid has been investigated for its role in the development of materials with antimicrobial properties, which could be incorporated into products to prevent the spread of infections and improve hygiene.
Used in Neurodegenerative Disease Treatment:
5-tert-butylpyridine-2-carboxylic acid is explored for its potential role in the treatment of neurodegenerative diseases due to its ability to modulate certain neurotransmitter receptors in the brain, offering a new avenue for therapeutic intervention in conditions such as Alzheimer's and Parkinson's diseases.
Overall, 5-tert-butylpyridine-2-carboxylic acid's diverse applications and ongoing research across different fields highlight its significance as a chemical compound with broad potential impact.

Check Digit Verification of cas no

The CAS Registry Mumber 1005785-85-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,5,7,8 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1005785-85:
(9*1)+(8*0)+(7*0)+(6*5)+(5*7)+(4*8)+(3*5)+(2*8)+(1*5)=142
142 % 10 = 2
So 1005785-85-2 is a valid CAS Registry Number.

1005785-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-tert-butylpyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-TERBUTYLPIEOLINIC 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:1005785-85-2 SDS

1005785-85-2Downstream Products

1005785-85-2Relevant academic research and scientific papers

INFLUENZA VIRUS INHIBITOR TARGETING NUCLEOPROTEIN

-

Paragraph 0112, (2019/06/09)

This document discloses a novel class of compound for treating influenza A and influenza B viral infection, and compositions and methods of use thereof.

HETEROARYL COMPOUNDS AS BTK INHIBITORS AND USES THEREOF

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, (2016/05/02)

The present invention relates to imidazo pyridine compounds, and pharmaceutically acceptable compositions thereof, useful as BTK inhibitors.

Aromatic ring cleavage of 2-amino-4-tert-butylphenol by a nonheme iron(II) complex: Functional model of 2-aminophenol dioxygenases

Chakraborty, Biswarup,Paine, Tapan Kanti

supporting information, p. 920 - 924 (2013/03/13)

Biomimetic aromatic ring cleavage: An iron(II)-2-aminophenolate complex (see picture, right) with a tetradentate ligand reacts with dioxygen to cleave the aromatic C-C bond of 2-amino-4-tert-butylphenolate to form 4-tert-butyl-2-picolinate. This complex represents a functional model of 2-aminophenol-1,6-dioxygenase (APD) and 3-hydroxyanthranilate-3,4-dioxygenase (HAD). Copyright

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