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(E)-2,3-Dibromopropenoic acid, with the molecular formula C3H3Br2O2, is a carboxylic acid featuring two bromine atoms and a double bond in its structure. This chemical compound is predominantly utilized in the realm of chemical research and serves as a fundamental building block for the synthesis of a wide array of organic compounds. Its unique structure allows it to participate in various reactions, leading to the formation of different derivatives. Beyond its applications in chemical research and synthesis, (E)-2,3-Dibromopropenoic acid also holds potential for use in the pesticide industry and pharmaceutical manufacturing. However, due to its potential toxicity and environmental hazards, it is crucial to handle (E)-2,3-Dibromopropenoic acid with caution.

1578-72-9

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1578-72-9 Usage

Uses

Used in Chemical Research:
(E)-2,3-Dibromopropenoic acid is used as a research compound for [exploring its chemical properties and reactivity] in chemical reactions.
Used in Organic Synthesis:
(E)-2,3-Dibromopropenoic acid is used as a building block for [synthesizing various organic compounds] due to its unique structure and reactivity.
Used in Pesticide Industry:
(E)-2,3-Dibromopropenoic acid is used as a potential active ingredient for [developing new pesticides], given its chemical properties.
Used in Pharmaceutical Manufacturing:
(E)-2,3-Dibromopropenoic acid is used as a starting material for [manufacturing certain pharmaceuticals], taking advantage of its ability to form different derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 1578-72-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1578-72:
(6*1)+(5*5)+(4*7)+(3*8)+(2*7)+(1*2)=99
99 % 10 = 9
So 1578-72-9 is a valid CAS Registry Number.

1578-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2,3-dibromo-4-methylpent-2-enoic acid

1.2 Other means of identification

Product number -
Other names 2,3c-Dibrom-acrylsaeure

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:1578-72-9 SDS

1578-72-9Upstream product

1578-72-9Downstream Products

1578-72-9Relevant academic research and scientific papers

Carboxylate-directed tandem functionalisations of α,β- dihaloalkenoic acids with 1-alkynes: A straightforward access to (Z)-configured, α,β-substituted γ-alkylidenebutenolides

Inack Ngi, Samuel,Cherry, Khalil,Héran, Virginie,Commeiras, Laurent,Parrain, Jean-Luc,Duchêne, Alain,Abarbri, Mohamed,Thibonnet, Jér?me

supporting information; experimental part, p. 13692 - 13696 (2012/01/06)

An easy and mild copper(I)-catalysed lactonisation of readily available (E)-2,3-dihalopropenoic acid derivatives regio- and stereoselectively leads to rarely described (Z)-3-halo-5-ylidene-5H-furan-2-ones. These compounds are subsequently able to undergo classical Pd-catalysed cross-coupling reactions, providing 3-substituted and 3,4-disubstituted 5-ylidene-5H-furan-2-ones (see scheme).

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