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5-Bromo-2,3-dimethylpyridine, with the molecular formula C7H8BrN, is a pyridine derivative featuring a bromine atom and two methyl groups attached to the 2 and 3 positions of the ring. This chemical compound is recognized for its unique structure and reactivity, making it a valuable intermediate in the synthesis of biologically active compounds.

27063-90-7

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27063-90-7 Usage

Uses

Used in Pharmaceutical Industry:
5-Bromo-2,3-dimethylpyridine is used as a building block in organic synthesis for its role in creating various biologically active compounds. Its unique structure contributes to the development of new pharmaceuticals, enhancing the range of treatments available for various health conditions.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 5-Bromo-2,3-dimethylpyridine serves as a key intermediate in the synthesis of active ingredients for pesticides and other agricultural chemicals, potentially improving crop protection and yield.
Used in Material Science:
5-Bromo-2,3-dimethylpyridine also has potential applications in the development of new materials, given its chemical properties. It can be utilized in the creation of advanced materials for various technological applications, including but not limited to sensors, catalysts, and other specialty chemicals.
Safety Note:
It is crucial to handle 5-Bromo-2,3-dimethylpyridine with care due to its potential hazards if not used properly. Adequate safety measures should be taken to ensure the safe use of this chemical compound in research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 27063-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,6 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27063-90:
(7*2)+(6*7)+(5*0)+(4*6)+(3*3)+(2*9)+(1*0)=107
107 % 10 = 7
So 27063-90-7 is a valid CAS Registry Number.

27063-90-7SDS

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 5-Bromo-2,3-dimethylpyridine

1.2 Other means of identification

Product number -
Other names PYRIDINE,5-BROMO-2,3-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:27063-90-7 SDS

27063-90-7Upstream product

27063-90-7Relevant academic research and scientific papers

PREPARATION OF OPTIONALLY SUBSTITUTED DIHYDROISOQUINOLINES

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Page/Page column 28, (2019/08/14)

Preparation of optionally substituted dihydroisoquinolines The present invention relates to a process for the preparation of optionally substituted dihydroi- soquinolines of the formula I

HALOGENATION OF PYRIDINE DERIVATIVES

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Page/Page column 21; 22, (2019/08/12)

The present invention relates to a process for the preparation of pyridine derivatives of the formula (I) comprising two steps, namely, a selective chlorination followed by a selective fluorination.

PREPARATION OF OPTIONALLY SUBSTITUTED 5-SUBSTITUTED PYRIDINE

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Page/Page column 25, (2019/08/12)

The present invention relates to a process for the preparation of optionally substituted 5-substituted pyridine of the formula I.

BROMINATION OF PYRIDINE DERIVATIVES

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Page/Page column 16, (2019/08/12)

The present invention relates to a process for the preparation pyridine derivatives of the formula (I).

BETA-LACTAMASE INHIBITORS

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Paragraph 0520, (2014/07/22)

Described herein are compounds and compositions that modulate the activity of beta-lactamases. In some embodiments, the compounds described herein inhibit beta-lactamase. In certain embodiments, the compounds described herein are useful in the treatment of bacterial infections.

SUBSTITUTED ISOCYTOSINES HAVING HISTAMINE H2-ANTAGONIST ACTIVITY

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, (2008/06/13)

The compounds are substituted isocytosines which are histamine H 2-antagonists. Two specific compounds of the present inventon are 2-2-(5-methyl-4-imidazolylmethylthio)ethylamino!-5-(3-pyridylmethyl)-4-pyrimi done and 2-2-(3-bromo-2-pyridylmethylthio)ethylamino!-5-(4-pyridylmethyl)-4-pyrimidone .

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