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1578-72-9

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1578-72-9 Usage

General Description

(E)-2,3-Dibromopropenoic acid is a chemical compound with the molecular formula C3H3Br2O2. It is a carboxylic acid with two bromine atoms and a double bond in its structure. The compound is mainly used in chemical research and as a building block for the synthesis of various organic compounds. It can also be involved in reactions to form different derivatives. Additionally, (E)-2,3-Dibromopropenoic acid is known for its potential use as a pesticide and in the manufacturing of pharmaceuticals. However, it is important to handle this chemical with care due to its potential toxicity and environmental hazards.

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 articles and documents

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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