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Zinc, bromo[3-(ethoxycarbonyl)phenyl]is a chemical compound characterized by a zinc atom bonded to a bromine atom and a phenyl group featuring an ethoxycarbonyl substituent. It is recognized for its role in promoting specific transformations in organic synthesis, making it a valuable reagent in the creation of pharmaceuticals, agrochemicals, and other significant chemicals. Moreover, its potential therapeutic properties are being explored for the treatment of various diseases and disorders, highlighting its importance in both organic chemistry and medicinal applications.

131379-38-9

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131379-38-9 Usage

Uses

Used in Organic Synthesis:
Zinc, bromo[3-(ethoxycarbonyl)phenyl]is utilized as a reagent in organic synthesis for its ability to facilitate specific chemical transformations. It is particularly instrumental in the preparation of complex organic molecules, which are essential in the development of pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, zinc, bromo[3-(ethoxycarbonyl)phenyl]is employed as a key intermediate in the synthesis of various drugs. Its unique properties allow for the creation of molecules with specific therapeutic effects, contributing to the advancement of new medications for the treatment of different diseases and disorders.
Used in Agrochemical Industry:
Zinc, bromo[3-(ethoxycarbonyl)phenyl]also plays a significant role in the agrochemical industry, where it is used in the synthesis of compounds with pesticidal or herbicidal properties. Its application helps in the development of more effective and environmentally friendly agrochemicals to protect crops and enhance agricultural productivity.
Used in Research and Development:
In the field of research and development, zinc, bromo[3-(ethoxycarbonyl)phenyl]is studied for its potential therapeutic properties. Scientists are exploring its use in the treatment of certain diseases and disorders, with the aim of discovering new therapeutic agents that can improve patient outcomes and contribute to better healthcare solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 131379-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,7 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 131379-38:
(8*1)+(7*3)+(6*1)+(5*3)+(4*7)+(3*9)+(2*3)+(1*8)=119
119 % 10 = 9
So 131379-38-9 is a valid CAS Registry Number.

131379-38-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name bromozinc(1+),ethyl benzoate

1.2 Other means of identification

Product number -
Other names p-Ethoxycarbonylphenylzinc bromide

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:131379-38-9 SDS

131379-38-9Relevant academic research and scientific papers

Synthesis of Symmetrical Diaryl Ketones by Cobalt-Catalyzed Reaction of Arylzinc Reagents with Ethyl Chloroformate

Rérat, Alice,Michon, Christophe,Agbossou-Niedercorn, Francine,Gosmini, Corinne

, p. 4554 - 4560 (2016/09/23)

Symmetrical diaryl ketones were prepared by a cross-coupling reaction between aryl bromides and ethyl chloroformate. This new method, which uses a catalyst composed of CoBr2and a bipyridine ligand along with readily available starting materials, allows for the synthesis of a variety of symmetrical diaryl ketones in moderate to excellent yields (37–99 %) under mild conditions. This reaction, in which ethyl chloroformate acts as a surrogate of carbon monoxide in the presence of cobalt and zinc, represents an interesting alternative to previously known approaches for the synthesis of diarylmethanones.

IONIC LIQUID SUPPORTED ORGANOTIN REAGENTS FOR THE MANUFACTURING OF RADIOPHARMACEUTICALS COMPOUNDS

-

Page/Page column 81; 82, (2015/07/23)

The present invention relates to an ionic liquid supported organotin reagent of formula (I). The invention further relates to a process for manufacturing the ionic liquid supported organotin reagent of formula (I) and to a process for manufacturing an hal

Microwave-assisted Negishi and Kumada cross-coupling reactions of aryl chlorides

Walla, Peter,Kappe, C. Oliver

, p. 564 - 565 (2007/10/03)

Rapid Pd or Ni-catalyzed microwave-accelerated Negishi and Kumada cross-coupling reactions of aryl chlorides in solution and on solid phase are reported.

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