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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-Propenenitrile, 3-(3,4-dimethoxyphenyl)-

N#C/C=C/c1ccc(c(c1)OC)OC Request for Quotation
Chemical Name: 2-Propenenitrile, 3-(3,4-dimethoxyphenyl)-
CAS Number: 6443-72-7
Product Number: AG003II6(AGN-PC-0JM2QU)
Synonyms:
MDL No:
Molecular Formula: C11H11NO2
Molecular Weight: 189.2105

Identification/Properties

Properties
MP:
181-184 °C
BP:
339.2 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302+H312+H332
Precautionary Statements:
P280
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3-(3,4-Dimethoxyphenyl)acrylonitrile, also known as $name$, serves as a versatile building block in chemical synthesis. Its unique structure and reactivity make it a valuable intermediate in the production of various organic compounds.1. Cross-Coupling Reactions: 3-(3,4-Dimethoxyphenyl)acrylonitrile can undergo cross-coupling reactions with different organometallic reagents, such as Grignard reagents or organozinc compounds. These reactions enable the formation of more complex molecules by introducing new functional groups at the acrylonitrile moiety.2. Heterocyclic Chemistry: The acrylonitrile group in this compound can participate in cyclization reactions to form heterocycles. By manipulating reaction conditions and solvent systems, chemists can selectively synthesize diverse heterocyclic structures, including pyrroles, pyrrolines, or indoles.3. Electrophilic Aromatic Substitution: The presence of the dimethoxyphenyl group provides electron-donating properties, making the compound prone to electrophilic aromatic substitution reactions. This reactivity can be harnessed to introduce substituents onto the phenyl ring, leading to the synthesis of substituted aromatic compounds.In summary, 3-(3,4-Dimethoxyphenyl)acrylonitrile plays a crucial role in chemical synthesis by serving as a key intermediate for the construction of complex organic molecules through various synthetic pathways.