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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)-

Benzenebutanoic acid, 3-hydroxy-, ethyl ester

CCOC(=O)CCCc1cccc(c1)O Request for Quotation
Chemical Name: Benzenebutanoic acid, 3-hydroxy-, ethyl ester
CAS Number: 160721-25-5
Product Number: AG001VA7(AGN-PC-0045EM)
Synonyms:
MDL No:
Molecular Formula: C12H16O3
Molecular Weight: 208.2536

Identification/Properties

Properties
BP:
335.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
208.257g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
208.11g/mol
Monoisotopic Mass:
208.11g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
191
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The Ethyl 4-(3-hydroxyphenyl)butanoate compound is widely utilized in chemical synthesis as a key intermediate in various processes. With its unique structure and properties, this versatile compound plays a crucial role in the production of a range of valuable materials. In organic synthesis, Ethyl 4-(3-hydroxyphenyl)butanoate is frequently employed as a precursor for the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its versatile nature allows it to be utilized in the creation of complex molecules through various chemical transformations, making it an essential building block in the synthesis of diverse compounds. The application of Ethyl 4-(3-hydroxyphenyl)butanoate in chemical synthesis demonstrates its significance in modern organic chemistry and highlights its potential for facilitating the development of innovative products.