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2-Bromo-4,5-dimethyl-pyridine, with the molecular formula C7H8BrN, is a pyridine derivative featuring two methyl groups and a bromine atom attached to the pyridine ring. This organic compound is recognized for its versatility as a building block in organic synthesis, enabling it to participate in a variety of chemical reactions such as nucleophilic substitution and metal-catalyzed coupling reactions. It is a valuable reagent in the field of organic chemistry, particularly for its role in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

66533-31-1

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66533-31-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-4,5-dimethyl-pyridine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be readily modified through chemical reactions, contributing to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromo-4,5-dimethyl-pyridine serves as an essential component in the creation of pesticides and other agricultural chemicals, leveraging its reactivity to form compounds with pesticidal activity.
Used in Organic Synthesis:
2-Bromo-4,5-dimethyl-pyridine is utilized as a versatile reagent in organic synthesis, allowing for the production of a wide range of organic compounds through its participation in nucleophilic substitution and metal-catalyzed coupling reactions, thus expanding the scope of accessible chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 66533-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,3 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66533-31:
(7*6)+(6*6)+(5*5)+(4*3)+(3*3)+(2*3)+(1*1)=131
131 % 10 = 1
So 66533-31-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H8BrN/c1-5-3-7(8)9-4-6(5)2/h3-4H,1-2H3

66533-31-1SDS

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-Bromo-4,5-dimethylpyridine

1.2 Other means of identification

Product number -
Other names Pyridine,2-bromo-4,5-dimethyl

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:66533-31-1 SDS

66533-31-1Upstream product

66533-31-1Relevant academic research and scientific papers

SUBSTITUTED DIPYRIDYL-DIHYDROPYRAZOLONES AND USE THEREOF

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Page/Page column 23, (2010/04/30)

The present application relates to novel substituted dipyridyldihydropyrazolone derivatives, processes for their preparation, their use for treatment and/or prophylaxis of diseases and their use for the preparation of medicaments for treatment and/or prophylaxis of diseases, in particular cardiovascular and hematological diseases and kidney diseases, and for promoting wound healing.

SUBSTITUTED DIHYDROPYRAZOLONES FOR TREATING CARDIOVASCULAR AND HEMATOLOGICAL DISEASES

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Page/Page column 19, (2010/12/29)

The invention relates to dihydropyrazolon-derivatives of formula (I), to methods for their production, to their use for treating and/or for preventing diseases and their use for producing medicaments for treating and/or for preventing diseases, in particular cardiovascular and haematological diseases, kidney diseases and for promoting the healing of wounds.

METHOD FOR SYNTHESIS OF IRIDUIM (III) COMPLEXES WITH STERICALLY DEMANDING LIGANDS

-

, (2009/05/28)

Phosphorescent materials and devices with improved device manufacturing, fabrication, stability, efficiency, and/or color.

Side-chain retention during lithiation of 4-picoline and 3,4-lutidine: Easy access to molecular diversity in pyridine series

Kaminski, Thomas,Gros, Philippe,Fort, Yves

, p. 3855 - 3860 (2007/10/03)

The first direct ring-selective lithiation of 4-picoline and 3,4-lutidine has been achieved through the use of BuLi/LiDMAE aggregates to prevent the usual side-chain metallation. Several functionalities have been introduced at the C-2, C-6 and C-5 positions by ring-selective sequential lithiation, opening a simple and fast route to polysubstituted pyridine building blocks. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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