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2,6-dichloro-N-Methylpyridin-4-aMine is a chemical compound characterized by the molecular formula C6H6Cl2N2. It is a pyridine derivative featuring two chlorine atoms and a methyl group attached to the pyridine ring, which endows it with unique chemical properties. 2,6-dichloro-N-Methylpyridin-4-aMine is recognized for its role as an intermediate in the synthesis of pharmaceutical and agrochemical products, and it is also under investigation for its potential therapeutic applications in neurological disorders.

175461-33-3

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175461-33-3 Usage

Uses

Used in Pharmaceutical Synthesis:
2,6-dichloro-N-Methylpyridin-4-aMine is utilized as a key intermediate in the production of various pharmaceuticals. Its unique structure allows it to be a building block for the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Agrochemical Production:
In the agrochemical industry, 2,6-dichloro-N-Methylpyridin-4-aMine serves as an essential intermediate for the synthesis of pesticides and other crop protection agents. Its chemical properties make it suitable for creating compounds that can effectively control pests and diseases in agriculture.
Used in Neurological Disorder Research:
2,6-dichloro-N-Methylpyridin-4-aMine is also being explored for its potential in the treatment of neurological disorders. Its specific chemical structure may offer new avenues for therapeutic intervention, providing a basis for the development of novel treatments for conditions such as Alzheimer's, Parkinson's, or other neurodegenerative diseases.
Overall, 2,6-dichloro-N-Methylpyridin-4-aMine is a versatile compound with applications spanning across pharmaceuticals, agrochemicals, and medical research, highlighting its significance in the fields of chemistry and biology.

Check Digit Verification of cas no

The CAS Registry Mumber 175461-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,4,6 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 175461-33:
(8*1)+(7*7)+(6*5)+(5*4)+(4*6)+(3*1)+(2*3)+(1*3)=143
143 % 10 = 3
So 175461-33-3 is a valid CAS Registry Number.

175461-33-3Downstream Products

175461-33-3Relevant academic research and scientific papers

NOVEL COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF FOR THE TREATMENT OF INFLAMMATORY DISORDERS

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Paragraph 0476, (2017/02/09)

The present invention discloses compounds according to Formula (I), wherein R1, R3, R4, R5, L1, and Cy are as defined herein. The present invention also provides compounds, methods for the production of said compounds of the invention, pharmaceutical compositions comprising the same and their use in allergic or inflammatory conditions, autoimmune diseases, proliferative diseases, transplantation rejection, diseases involving impairment of cartilage turnover, congenital cartilage malformations, and/or diseases associated with hypersecretion of IL6 and/or interferons. The present invention also methods for the prevention and/or treatment of the aforementioned diseases by administering a compound of the invention.

Synthesis and evaluation of novel imidazo[4,5-: C] pyridine derivatives as antimycobacterial agents against Mycobacterium tuberculosis

Madaiah, Malavalli,Prashanth, Maralekere K.,Revanasiddappa, Hosakere D.,Veeresh, Bantal

, p. 9194 - 9204 (2016/11/11)

The current study involves the synthesis of novel imidazo[4,5-c]pyridine derivatives (IPD) containing amide/urea/sulfonamide. The synthesized compounds were evaluated for in vitro and in vivo antimycobacterial activities against Mycobacterium tuberculosis. The pharmacological activities were determined by the objective to better understand their structure-activity relationship (SAR) for their in vitro antimycobacterial activity against M. tuberculosis. Some synthesized compounds showed significant activity against M. tuberculosis based on the agar dilution method. Among the forty-one compounds screened, compounds 21, 22 and 23 were found to be the most active compounds against M. tuberculosis. In the in vivo animal model, 21, 22 and 23 decreased the bacterial load in lung and spleen tissues at the dose of 50 mg kg-1 body weight.

ALKYNYL ALCOHOLS AND METHODS OF USE

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Paragraph 0300; 0331; 0551; 0552, (2015/03/04)

The invention relates to compounds of Formula (0): wherein A1-A8, R4 and R5 each has the meaning as described herein. Compounds of Formula (0) and pharmaceutical compositions thereof are useful in the treatment of diseases and disorders in which undesired or over-activation of NF-kB signaling is observed.

ALKYNYL ALCOHOLS AND METHODS OF USE

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Page/Page column 91; 137; 138, (2015/03/13)

The invention relates to compounds of Formula (0): wherein A1-A8, R4 and R5 each has the meaning as described herein. Compounds of Formula (0) and pharmaceutical compositions thereof are useful in the treatment of diseases and disorders in which undesired or over-activation of NF-kB signaling is observed.

PYRIDINYL-PYRAZOLE DERIVATIVES AND THEIR USE AS POTASSIUM CHANNEL MODULATORS

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Page/Page column 22, (2008/12/07)

This invention relates to novel pyridinyl-pyrazole derivatives and their use as potassium channel modulating agents. Moreover the invention is directed to pharmaceutical compositions useful for the treatment or alleviation of diseases or disorders associa

8H-IMIDAZO[4,5-D]THIAZOLO[4,5-B]PYRIDINE BASED TRICYCLIC COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS COMPRISING SAME

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Page/Page column 57-58, (2008/06/13)

The present invention provides for thiazolopyridine-based tricyclic compounds having the formula (I) wherein R1, R2, R5 and R6 are as described herein. The present invention further provides pharmaceutical compo

1, 6 -DIHYDRO- 1,3, 5, 6-TETRAAZA-AS-INDACENE BASED TRICYCLIC COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS COMPRISING SAME AS INHIBITORS OF IKK ENZYME ACTIVITY

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Page/Page column 71-72, (2010/11/24)

The present invention provides for tricyclic compounds having the formula (I) wherein R1, R2, R5, R6, R7, and R8 are as described herein. The present invention further provides pharmaceutical compositions comprising such compounds, as well as the use of such compounds for treating inflammatory and immune diseases.

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