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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)-

Benzene, chloroethoxy-

ClCCOc1ccccc1 Request for Quotation
Chemical Name: Benzene, chloroethoxy-
CAS Number: 622-86-6
Product Number: AG00IAZO(AGN-PC-0JKAFZ)
Synonyms:
MDL No:
Molecular Formula: C8H9ClO
Molecular Weight: 156.6095

Identification/Properties

Computed Properties
Molecular Weight:
156.609g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
156.034g/mol
Monoisotopic Mass:
156.034g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
79.3
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


2-Phenoxyethyl chloride, also known as phenyl glycidyl ether or 1-chloro-2-phenoxyethane, is a versatile chemical compound commonly used in chemical synthesis processes. This organic compound is primarily utilized as a key intermediate in the production of various pharmaceuticals, agricultural chemicals, and other fine chemicals. In chemical synthesis, 2-Phenoxyethyl chloride serves as a crucial building block for the creation of more complex molecules. Its reactivity allows for the introduction of the phenoxyethyl group into organic frameworks, enabling the formation of new carbon-carbon or carbon-oxygen bonds. This compound can undergo various types of reactions, such as nucleophilic substitution and addition reactions, facilitating the development of diverse chemical structures.Moreover, 2-Phenoxyethyl chloride exhibits good stability under typical storage conditions, making it a reliable reagent in organic chemistry laboratories. Its controlled handling and usage ensure efficient and reproducible chemical transformations, contributing to the success of synthetic routes in the development of target compounds. By incorporating 2-Phenoxyethyl chloride into synthetic schemes, chemists can access a wide array of functionalized molecules for further applications in research and industrial settings.