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6213-87-2

methyl (E)-3-bromoprop-2-enoate

Catalog#: AR00F43T  |   CAS#: 6213-87-2  |   MDL#: MFCD00154498  |   MF: C4H5BrO2  |   MW: 164.9853

Packsize Purity Price Availability Quantity
100mg 97% $130.00 Global Stock Buy Now Add To Cart
250mg 97% $231.00 Global Stock Buy Now Add To Cart
1g 97% $571.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00F43T
Chemical Name methyl (E)-3-bromoprop-2-enoate
CAS Number 6213-87-2
Molecular Formula C4H5BrO2
Molecular Weight 164.9853
MDL Number MFCD00154498
SMILES COC(=O)/C=C/Br

(E)-Methyl 3-bromoacrylate, also known as (E)-3-bromoacrylic acid methyl ester, is a valuable compound widely used in chemical synthesis. This versatile building block plays a crucial role in various organic reactions, particularly in the field of organic chemistry. (E)-Methyl 3-bromoacrylate is commonly utilized as a key intermediate in the synthesis of complex organic compounds due to its unique properties and reactivity.In chemical synthesis, (E)-Methyl 3-bromoacrylate serves as a precursor for the preparation of various functionalized molecules such as pharmaceuticals, agrochemicals, and materials. Its ability to undergo various chemical transformations, such as nucleophilic addition and cross-coupling reactions, makes it a valuable tool for organic chemists striving to build structurally diverse and intricate molecules.Moreover, the presence of the bromine atom in the molecule offers opportunities for further derivatization and functional group interconversion, allowing for the introduction of additional complexity in the molecular structure. This compound's versatility and reactivity make it an indispensable component in the toolbox of synthetic chemists working towards the creation of novel compounds with tailored properties and functionalities.Overall, (E)-Methyl 3-bromoacrylate's utility in chemical synthesis stems from its role as a versatile and reactive building block that enables the efficient construction of complex organic molecules through strategic transformations and functional group manipulations.
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