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2-(2-Bromo-ethyl)-pyridine hydrobromide is a chemical compound characterized by a pyridine ring with a 2-bromo-ethyl substituent and a hydrobromide salt. 2-(2-BROMO-ETHYL)-PYRIDINE HYDROBROMIDE is recognized for its utility in organic synthesis, especially in the creation of pharmaceuticals and fine chemicals. The presence of a bromine atom on the ethyl group endows the compound with properties that make it a valuable intermediate for the synthesis of biologically active molecules. Furthermore, the hydrobromide salt form enhances its solubility in polar solvents, facilitating its use in laboratory settings. It is a versatile chemical with a broad spectrum of applications in organic chemistry.

72996-65-7

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72996-65-7 Usage

Uses

Used in Pharmaceutical Industry:
2-(2-Bromo-ethyl)-pyridine hydrobromide is used as a synthetic intermediate for the production of various pharmaceuticals due to its ability to be incorporated into the molecular structures of drugs, contributing to their therapeutic effects.
Used in Organic Synthesis:
In the field of organic chemistry, 2-(2-Bromo-ethyl)-pyridine hydrobromide serves as a reagent for the synthesis of a wide range of organic compounds, leveraging its unique structural features to form new chemical entities with potential applications.
Used in Fine Chemicals Production:
2-(2-Bromo-ethyl)-pyridine hydrobromide is utilized as a key component in the manufacture of fine chemicals, where its specific chemical properties are harnessed to produce high-quality specialty chemicals for various industries.
Used in Laboratory Research:
As a compound with increased solubility in polar solvents, 2-(2-Bromo-ethyl)-pyridine hydrobromide is used in laboratory research to facilitate chemical reactions and experiments, making it easier to work with due to its solubility and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 72996-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,9 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72996-65:
(7*7)+(6*2)+(5*9)+(4*9)+(3*6)+(2*6)+(1*5)=177
177 % 10 = 7
So 72996-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H8BrN.BrH/c8-5-4-7-3-1-2-6-9-7;/h1-3,6H,4-5H2;1H

72996-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-Bromo-Ethyl)-Pyridine Hydrobromide

1.2 Other means of identification

Product number -
Other names 2-(2-bromoethyl)pyridine,hydrobromide

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:72996-65-7 SDS

72996-65-7Relevant academic research and scientific papers

PROCESS AND INTERMEDIATES FOR THE PREPARATION OF PERAMPANEL

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Page/Page column 21; 24; 25, (2016/09/15)

The present invention describes a process for the synthesis of 3-(2-cyanophenyl)-5-(2- pyridyl)-1-phenyl-1,2-dihydro-pyridin-2-one (Perampanel) represented by the structure of formula (1), and salts thereof, especially salts with pharmaceutically acceptable acids. The present invention further relates to certain intermediates formed and/or used in such process.

Compounds comprising linked heteroaryl moieties and their use as novel umami flavor modifiers, tastants and taste enhancers for comestible compositions

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Page/Page column 37, (2010/11/24)

The inventions disclosed herein relate to the discovery of the use of compounds having the formula shown below and certain subgenera or species thereof, as flavor or taste modifiers, particularly, savory (“umami”) taste modifiers, savory flavoring agents

Spiro Derivatives of Tetrahydrothiophene. Synthesis of the Quinolizidinetetrahydrothiophene System Using Solid/Liquid or Liquid/Liquid Phase-Transfer Catalysis

Wrobel, Jerzy T.,Hejchman, Elzbieta

, p. 452 - 455 (2007/10/02)

4-Oxooctahydroquinolizinetetrahydrothiophene 1',1'-dioxide can be synthetized from 2-cyanotetrahydrothiophene by two independent routes, both of them using phase-transfer catalysis: the first one involves alkylation of 2-cyanotetrahydrothiphen

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