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2,5-Dibromopentanoic acid ethyl ester is a chemical compound characterized by the molecular formula C7H11Br2O2. It is an ester that results from the esterification of 2,5-dibromopentanoic acid with ethanol. This colorless to pale yellow liquid possesses a strong, pleasant odor and is utilized in various organic synthesis processes and as a reagent in chemical reactions.

29823-16-3

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29823-16-3 Usage

Uses

Used in Organic Synthesis:
2,5-Dibromopentanoic acid ethyl ester serves as a key intermediate in organic synthesis, facilitating the creation of a range of chemical compounds. Its unique structure, featuring two bromine atoms, makes it a valuable building block for the synthesis of complex organic molecules.
Used in Chemical Reactions as a Reagent:
In the realm of chemical reactions, 2,5-Dibromopentanoic acid ethyl ester is employed as a reagent, contributing to the formation of desired products through various chemical processes. Its reactivity and functional groups make it suitable for use in a multitude of reactions, including substitution, addition, and elimination reactions.
Used in Pharmaceutical Industry:
2,5-Dibromopentanoic acid ethyl ester is utilized in the pharmaceutical industry for the synthesis of pharmaceutical compounds. Its unique properties and reactivity allow for the development of new drugs and the modification of existing ones, potentially leading to improved therapeutic agents.
Used in Research and Development:
In the field of research and development, 2,5-Dibromopentanoic acid ethyl ester is used to explore new chemical reactions and mechanisms. Its versatility as a reagent and intermediate enables scientists to investigate novel pathways and reactions, contributing to the advancement of chemical knowledge.
Safety and Handling:
Given its flammable nature, 2,5-Dibromopentanoic acid ethyl ester requires careful handling and storage. It is essential to follow proper safety and handling procedures to minimize risks associated with its use. This includes using appropriate personal protective equipment, working in well-ventilated areas, and storing the compound away from heat and open flames.

Check Digit Verification of cas no

The CAS Registry Mumber 29823-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,2 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29823-16:
(7*2)+(6*9)+(5*8)+(4*2)+(3*3)+(2*1)+(1*6)=133
133 % 10 = 3
So 29823-16-3 is a valid CAS Registry Number.

29823-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2,5-dibromopentanoate

1.2 Other means of identification

Product number -
Other names 2,5-dibromo-valeric acid ethyl ester

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:29823-16-3 SDS

29823-16-3Relevant academic research and scientific papers

Process for the preparation of bicyclic compounds and the use of this process for the preparation of an ice inhibitor compound

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, (2008/06/13)

A method for preparing compounds of formula (I) wherein R is selected from the group consisting of H. alkyl, aryl, and aralkyl of up to 18 carbon atoms and the amine function may be free or protected from a compound of formula (IA) wherein cyclization is carried out in a basic medium and in the presence of a phosphonic acid derivative and the use of said method as an intermediate step for preparing a compound inhibiting the interleukin-1 beta conversion enzyme.

Derivatives of octahydro-6,10-dioxo-6H-pyridazino [1,2-a] [1,2] diazepine-1-carboxylic acid, their preparation process and their use in the preparation of therapeutically active compounds

-

, (2008/06/13)

Novel intermediates of the formulae where the substituents are defined as in the specification.

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