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2,6-Dichloro-N4-methylpyridine-3,4-diamine is a chemical compound characterized by a pyridine ring with a methyl group, two chlorine atoms at the 2 and 6 positions, and two amino groups at the 3 and 4 positions. This versatile molecule is known for its strong odor and is classified as a dangerous substance, necessitating careful handling and disposal. It serves as a valuable building block in the synthesis of pharmaceuticals and agrochemicals, contributing to the creation of diverse chemical structures.

914942-86-2

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914942-86-2 Usage

Uses

Used in Pharmaceutical Industry:
2,6-Dichloro-N4-methylpyridine-3,4-diamine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications, making it an essential component in the medicinal chemistry field.
Used in Agrochemical Industry:
In the agrochemical sector, 2,6-Dichloro-N4-methylpyridine-3,4-diamine is employed as a building block for the production of pesticides and other agrochemicals. Its incorporation into these compounds can lead to the development of more effective and targeted products for agricultural use, enhancing crop protection and yield.
Used in Chemical Research:
2,6-Dichloro-N4-methylpyridine-3,4-diamine is also utilized in academic and industrial research settings as a model compound for studying chemical reactions and mechanisms. Its reactivity and structural features make it a valuable tool for understanding the behavior of similar compounds and advancing the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 914942-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,9,4 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 914942-86:
(8*9)+(7*1)+(6*4)+(5*9)+(4*4)+(3*2)+(2*8)+(1*6)=192
192 % 10 = 2
So 914942-86-2 is a valid CAS Registry Number.

914942-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dichloro-4-N-methylpyridine-3,4-diamine

1.2 Other means of identification

Product number -
Other names 2,6-Dichloro-N4-methylpyridine-3,4-diamine

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:914942-86-2 SDS

914942-86-2Relevant academic research and scientific papers

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.

NOVEL TRIAZOLOPYRIMIDINONE OR TRIAZOLOPYRIDINONE DERIVATIVES, AND USE THEREOF

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Paragraph 516; 517; 518; 519; 533; 534; 535, (2016/01/25)

The present invention relates to a novel triazolopyrimidinone or triazolopyridinone derivative, a tautomer thereof, a stereoisomer thereof and their mixture, or a pharmaceutically acceptable salt thereof; and a pharmaceutical composition for preventing or treating a tankyrase-related disease, which contains the same as an active ingredient.

ALKYNYL ALCOHOLS AND METHODS OF USE

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Paragraph 0555; 0556, (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 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.

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 74, (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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