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3,6-Dibromo-4-Methyl-pyridazine is a heterocyclic organic compound characterized by a pyridazine ring with bromine and methyl substituents at the 3 and 6 positions, respectively. With the molecular formula C6H5Br2N2, this chemical serves as a versatile intermediate in various chemical syntheses and has potential applications in pharmaceuticals, agrochemicals, materials science, and organic chemistry research.

89284-10-6

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89284-10-6 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
3,6-Dibromo-4-Methyl-pyridazine is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with specific biological activities, contributing to the advancement of drug discovery and crop protection.
Used in Organic Synthesis:
As a building block in organic synthesis, 3,6-Dibromo-4-Methyl-pyridazine is utilized for the construction of complex organic molecules. Its reactivity and functional group compatibility make it a valuable component in the synthesis of a wide range of organic compounds.
Used in Materials Science:
3,6-Dibromo-4-Methyl-pyridazine has potential applications in materials science, where its unique properties can be harnessed to develop new materials with specific characteristics. Its use in this field can lead to the creation of innovative materials with applications in various industries.
Used as a Research Tool in Organic Chemistry:
3,6-Dibromo-4-Methyl-pyridazine serves as a valuable research tool in the field of organic chemistry. Its reactivity and structural features make it an ideal candidate for studying various chemical reactions and mechanisms, contributing to the understanding and advancement of organic chemistry.
It is crucial to handle 3,6-Dibromo-4-Methyl-pyridazine with care, as it may pose hazards to human health and the environment. Proper safety measures and disposal methods should be followed to minimize any potential risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 89284-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,8 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89284-10:
(7*8)+(6*9)+(5*2)+(4*8)+(3*4)+(2*1)+(1*0)=166
166 % 10 = 6
So 89284-10-6 is a valid CAS Registry Number.

89284-10-6SDS

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 3,6-dibromo-4-methylpyridazine

1.2 Other means of identification

Product number -
Other names 3,6-Dibrom-4-methyl-pyridazin

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:89284-10-6 SDS

89284-10-6Downstream Products

89284-10-6Relevant academic research and scientific papers

HETEROARYL PIPERIDINE ETHER ALLOSTERIC MODULATORS OF THE M4 MUSCARINIC ACETYLCHOLINE RECEPTOR

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Page/Page column 47; 48, (2018/07/29)

The present invention is directed to heteroarylpiperidine ether compounds which are allosteric modulators of the M4 muscarinic acetylcholine receptor. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which M4 muscarinic acetylcholine receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which M4 muscarinic acetylcholine receptors are involved.

SUBSTITUTED TETRAHYDROQUINOLINONE COMPOUNDS AS ROR GAMMA MODULATORS

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Page/Page column 44, (2016/12/07)

The present invention provides substituted tetrahydroquinolinone and related compounds of formula (I), which are therapeutically useful as modulators of Retinoic acid receptor-related orphan receptors (RORs), more particularly as RORγ modulators. These co

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