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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)-

Phenol, 4-(2-bromoethoxy)-

BrCCOc1ccc(cc1)O Request for Quotation
Chemical Name: Phenol, 4-(2-bromoethoxy)-
CAS Number: 31406-95-8
Product Number: AG00C0UB(AGN-PC-0NKHB0)
Synonyms:
MDL No:
Molecular Formula: C8H9BrO2
Molecular Weight: 217.0599

Identification/Properties

Properties
Storage:
Room Temperature;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Phenol, 4-(2-bromoethoxy)- is a versatile chemical compound commonly used in chemical synthesis for a variety of applications. This compound serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and specialty chemicals due to its unique reactivity and functional group compatibility. In organic synthesis, Phenol, 4-(2-bromoethoxy)- can be used as a precursor in the formation of complex molecules through various reactions such as nucleophilic substitution, cross-coupling, and radical reactions. Its bromoethoxy group provides a site for further functionalization, allowing for the introduction of various substituents to tailor the properties of the final product. Additionally, Phenol, 4-(2-bromoethoxy)- can participate in the synthesis of polymers, surfactants, and organic dyes, expanding its utility across different industries. Its versatility and reactivity make it a valuable tool for chemists and researchers seeking to design and develop novel compounds with specific functions and applications.