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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-(3-ethoxyphenyl)-

CCOc1cccc(c1)/C=C/C(=O)O Request for Quotation
Chemical Name: 2-Propenoic acid, 3-(3-ethoxyphenyl)-
CAS Number: 103986-73-8
Product Number: AG003UXA(AGN-PC-0KL1L1)
Synonyms:
MDL No:
Molecular Formula: C11H12O3
Molecular Weight: 192.2112

Identification/Properties

Properties
MP:
131-133℃(lit.)
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
192.214g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
192.079g/mol
Monoisotopic Mass:
192.079g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
211
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(3-Ethoxyphenyl)acrylic acid, also known as ethyl 3-(3-ethoxyphenyl)acrylate, is a versatile compound commonly used in chemical synthesis processes. This compound serves as a key intermediate in the preparation of various organic compounds and materials. Its unique chemical structure allows for facile modification and manipulation, making it a valuable building block in the creation of complex molecules.One primary application of 3-(3-ethoxyphenyl)acrylic acid in chemical synthesis is its use in the synthesis of pharmaceuticals. By incorporating this compound into the synthesis pathway, chemists can introduce specific functional groups or stereochemistry required for the desired drug molecule. Its reactivity and compatibility with other reagents make it a valuable tool in medicinal chemistry for developing new therapeutic agents.Additionally, 3-(3-ethoxyphenyl)acrylic acid finds utility in the preparation of specialty polymers and materials. Its ability to undergo polymerization reactions allows for the creation of customized polymers with tailored properties such as solubility, thermal stability, and mechanical strength. These polymers can be applied in various industries, including coatings, adhesives, and electronics, where specific material characteristics are crucial.Furthermore, this compound can be used in the synthesis of fine chemicals and agrochemicals. Its versatile nature enables chemists to introduce specific functional groups that enhance the efficacy and selectivity of these chemical compounds. By incorporating 3-(3-ethoxyphenyl)acrylic acid into the synthetic route, researchers can access a broader range of structurally diverse molecules with improved properties for various applications.