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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-(3,4-dihydroxyphenyl)-, ethyl ester, (2E)-

CCOC(=O)/C=C/c1ccc(c(c1)O)O Request for Quotation
Chemical Name: 2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester, (2E)-
CAS Number: 66648-50-8
Product Number: AG003Q6I(AGN-PC-0OFUE0)
Synonyms:
MDL No:
Molecular Formula: C11H12O4
Molecular Weight: 208.21058

Identification/Properties

Properties
MP:
147～151℃
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
208.213g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
208.074g/mol
Monoisotopic Mass:
208.074g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
237
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
Precautionary Statements:
P261-P280-P305+P351+P338-P304+P340-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(E)-Ethyl Dihydroxycinnamate, also known as ethyl 3,4-dihydroxycinnamate, is a versatile compound widely used in chemical synthesis due to its unique reactivity and properties. This compound serves as a valuable building block for the synthesis of various organic molecules and pharmaceuticals. One of the key applications of (E)-Ethyl Dihydroxycinnamate in chemical synthesis is its role as a key intermediate in the preparation of cinnamoyl-based derivatives.In chemical synthesis, (E)-Ethyl Dihydroxycinnamate can undergo various chemical transformations such as esterification, oxidation, and reduction reactions to introduce functional groups and modify the structure of the molecule. Its distinctive structure with two hydroxyl groups and an ethyl ester moiety provides a platform for the introduction of diverse chemical functionalities, making it a valuable precursor for the synthesis of complex organic compounds.Furthermore, (E)-Ethyl Dihydroxycinnamate's ability to undergo selective reactions under specific conditions makes it a versatile tool for the development of novel molecules with tailored properties. Whether used as a starting material for natural product synthesis or as a key intermediate in pharmaceutical research, (E)-Ethyl Dihydroxycinnamate plays a crucial role in advancing the field of chemical synthesis and organic chemistry.