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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Butene, 2-bromo-, (2Z)-

C/C=C(Br)/C Request for Quotation
Chemical Name: 2-Butene, 2-bromo-, (2Z)-
CAS Number: 3017-68-3
Product Number: AG003CPN(AGN-PC-0O8Q7D)
Synonyms:
MDL No:
Molecular Formula: C4H7Br
Molecular Weight: 135.00238

Identification/Properties

Properties
MP:
-111.2°C
BP:
99.75°C
Storage:
2-8℃;
Form:
Liquid
Refractive Index:
n20/D 1.459(lit.)

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


(Z)-2-Bromo-2-butene is a versatile compound that plays a crucial role in chemical synthesis. This compound is commonly used as a key building block in organic chemistry reactions, particularly in the synthesis of various organic compounds. Its unique structure, with a bromine atom located on a terminal carbon of a butene chain in a trans configuration, provides opportunities for selective transformations in synthetic pathways.One important application of (Z)-2-Bromo-2-butene is in the preparation of complex organic molecules through cross-coupling reactions. By utilizing palladium-catalyzed coupling reactions, this compound can undergo efficient carbon-carbon bond formation with various nucleophiles, enabling the creation of new carbon-carbon bonds in a controlled manner. This strategy is widely employed in the synthesis of pharmaceuticals, agrochemicals, and materials with specific properties.Additionally, (Z)-2-Bromo-2-butene can act as a valuable precursor for the introduction of functional groups such as alkynes, alcohols, and amines through further derivatization reactions. Its selective reactivity at the allylic position allows chemists to access diverse molecular scaffolds with tailored functionalities, expanding the synthetic possibilities in drug discovery and material science.Overall, (Z)-2-Bromo-2-butene serves as a foundational compound in organic synthesis, enabling chemists to design efficient routes for the construction of complex molecules with desired properties and functionalities. Its strategic utilization in various synthetic methodologies highlights its significance in modern chemical research and development.