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Methyl 2,6-dichloro-4-cyanobenzoate is a chemical compound characterized by the molecular formula C9H5Cl2NO2. It is a white solid known for its high stability and low toxicity, making it a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals.

409127-32-8

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409127-32-8 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 2,6-dichloro-4-cyanobenzoate is used as an intermediate in the production of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the synthesis of a wide range of medications, contributing to the development of new and effective treatments.
Used in Agrochemical Industry:
Methyl 2,6-dichloro-4-cyanobenzoate is used as an intermediate in the synthesis of Pyridaben, a widely used acaricide effective against a variety of mites and ticks. Its role in the production of this acaricide helps protect crops and maintain agricultural productivity.
Used in Chemical Production:
Methyl 2,6-dichloro-4-cyanobenzoate is also utilized in the production of other chemicals, showcasing its versatility and importance in the chemical industry. Its high stability and low toxicity make it a preferred choice for various chemical synthesis processes.
Safety Considerations:
It is crucial to handle Methyl 2,6-dichloro-4-cyanobenzoate with care and follow safety guidelines when working with it in laboratory settings. Proper handling and storage are essential to ensure the safety of individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 409127-32-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,9,1,2 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 409127-32:
(8*4)+(7*0)+(6*9)+(5*1)+(4*2)+(3*7)+(2*3)+(1*2)=128
128 % 10 = 8
So 409127-32-8 is a valid CAS Registry Number.

409127-32-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2,6-dichloro-4-cyanobenzoate

1.2 Other means of identification

Product number -
Other names 2,6-dichloro-4-cyanobenzoic acid methylester

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:409127-32-8 SDS

409127-32-8Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS AS PROTEIN KINASE INHIBITORS

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Paragraph 0468, (2014/06/23)

The present invention provides a heterocyclic compound of formula (I), a pharmaceutically acceptable salt thereof, a prodrug thereof or a hydrate thereof, wherein A, A′ B, D, R1, R2 and R3 are as defined herein, a pharmaceutical composition comprising a compound of formula (I) as an active ingredient, methods of production, and methods of use thereof. Particularly, the present invention provides a compound of formula (I) useful for treating or preventing a disease, condition or disorder associated with protein kinases, preferably Janus Kinase family.

Lead optimization of a 4-aminopyridine benzamide scaffold to identify potent, selective, and orally bioavailable TYK2 inhibitors

Liang, Jun,Van Abbema, Anne,Balazs, Mercedesz,Barrett, Kathy,Berezhkovsky, Leo,Blair, Wade,Chang, Christine,Delarosa, Donnie,Devoss, Jason,Driscoll, Jim,Eigenbrot, Charles,Ghilardi, Nico,Gibbons, Paul,Halladay, Jason,Johnson, Adam,Kohli, Pawan Bir,Lai, Yingjie,Liu, Yanzhou,Lyssikatos, Joseph,Mantik, Priscilla,Menghrajani, Kapil,Murray, Jeremy,Peng, Ivan,Sambrone, Amy,Shia, Steven,Shin, Young,Smith, Jan,Sohn, Sue,Tsui, Vickie,Ultsch, Mark,Wu, Lawren C.,Xiao, Yisong,Yang, Wenqian,Young, Judy,Zhang, Birong,Zhu, Bing-Yan,Magnuson, Steven

, p. 4521 - 4536 (2013/07/25)

Herein we report our lead optimization effort to identify potent, selective, and orally bioavailable TYK2 inhibitors, starting with lead molecule 3. We used structure-based design to discover 2,6-dichloro-4-cyanophenyl and (1R,2R)-2-fluorocyclopropylamide modifications, each of which exhibited improved TYK2 potency and JAK1 and JAK2 selectivity relative to 3. Further optimization eventually led to compound 37 that showed good TYK2 enzyme and interleukin-12 (IL-12) cell potency, as well as acceptable cellular JAK1 and JAK2 selectivity and excellent oral exposure in mice. When tested in a mouse IL-12 PK/PD model, compound 37 showed statistically significant knockdown of cytokine interferon-γ (IFNγ), suggesting that selective inhibition of TYK2 kinase activity might be sufficient to block the IL-12 pathway in vivo.

HETEROCYCLIC COMPOUNDS AS PROTEIN KINASE INHIBITORS

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Page/Page column 77-78, (2012/12/13)

The present invention provides a heterocyclic compound of formula (I), a pharmaceutically acceptable salt thereof, a prodrug thereof or a hydrate thereof, wherein A, A' B, D, R1, R2 and R3 are as defined herein, a pharmaceutical composition comprising a compound of formula (I) as an active ingredient, methods of production, and methods of use thereof. Particularly, the present invention provides a compound of formula (I) useful for treating or preventing a disease, condition or disorder associated with protein kinases, preferably Janus Kinase family.

JANUS KINASE INHIBITOR COMPOUNDS AND METHODS

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Page/Page column 101, (2010/12/29)

The invention provides compounds of Formula I, stereoisomers or pharmaceutically acceptable salts thereof, wherein A, B, D, R1, R2, R4 and R5 are defined herein, a pharmaceutical composition that includes a compound of Formula I and methods of use thereof

New phenylalanine derivatives

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, (2008/06/13)

Specific phenylalanine derivatives or pharmaceutically acceptable. salts thereof have an antagonistic effect on the α4 integrins and, therefore, are usable as therapeutic agents or preventive agents for diseases in which α4 integrin-depending adhesion process participates in the pathology, such as inflammatory diseases, rheumatoid arthritis, inflammatory bowel diseases, systemic lupus erythematosus, multiple sclerosis, Sj?gren's syndrome, asthma, psoriasis, allergy, diabetes, cardiovascular diseases, arterial sclerosis, restenosis, tumor proliferation, tumor metastasis and transplantation rejection.

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