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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)-

Benzeneacetic acid, 3,5-dichloro-, ethyl ester

CCOC(=O)Cc1cc(Cl)cc(c1)Cl Request for Quotation
Chemical Name: Benzeneacetic acid, 3,5-dichloro-, ethyl ester
CAS Number: 200214-60-4
Product Number: AG002CMD(AGN-PC-03R2BY)
Synonyms:
MDL No:
Molecular Formula: C10H10Cl2O2
Molecular Weight: 233.0912

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
233.088g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
232.006g/mol
Monoisotopic Mass:
232.006g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
187
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzeneacetic acid, 3,5-dichloro-, ethyl ester plays a crucial role in chemical synthesis as a versatile building block. It is commonly utilized in the pharmaceutical industry for the synthesis of various drug compounds due to its functional groups and reactivity characteristics. This compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure enables it to undergo a variety of chemical reactions, including esterification, oxidation, and nucleophilic substitution, making it a valuable starting material for synthesizing complex organic molecules. Additionally, its 3,5-dichloro substituents provide opportunities for regioselective reactions, allowing chemists to control the specific placement of functional groups in the final product.