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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-Propenoic acid, 3-(1H-imidazol-4-yl)-, (2E)-

OC(=O)/C=C/c1c[nH]cn1 Request for Quotation
Chemical Name: 2-Propenoic acid, 3-(1H-imidazol-4-yl)-, (2E)-
CAS Number: 3465-72-3
Product Number: AG0032C4(AGN-PC-0O95VH)
Synonyms:
MDL No:
Molecular Formula: C6H6N2O2
Molecular Weight: 138.1240

Identification/Properties

Properties
MP:
225℃
BP:
456.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
138.126g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
138.043g/mol
Monoisotopic Mass:
138.043g/mol
Topological Polar Surface Area:
66A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
156
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(E)-3-(4-Imidazolyl)acrylic acid, also known as imidazole acrylic acid, is a versatile compound widely used in chemical synthesis. This compound is particularly valuable in organic chemistry as a key building block for the synthesis of various organic molecules. Its unique structure containing both an imidazole ring and an acrylic acid group provides a range of functional groups for diverse chemical reactions.One important application of (E)-3-(4-Imidazolyl)acrylic acid is in the synthesis of pharmaceutical compounds. The imidazole ring present in this compound is a common pharmacophore in many drug candidates, providing biological activity and enhancing drug-receptor interactions. By incorporating (E)-3-(4-Imidazolyl)acrylic acid into drug design, chemists can create new derivatives with improved therapeutic properties.Additionally, this compound is utilized in the preparation of advanced materials such as polymers and supramolecular assemblies. The acrylic acid moiety can undergo polymerization reactions to form crosslinked networks, while the imidazole group can coordinate with metal ions or other functional groups for the development of complex materials with tailored properties.In chemical synthesis, (E)-3-(4-Imidazolyl)acrylic acid serves as a versatile intermediate for the construction of diverse organic compounds through various synthetic routes. Its presence in the molecular structure imparts unique characteristics that enable the formation of novel molecules with potential applications across multiple fields, including pharmaceuticals, materials science, and biochemistry.