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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)-

Naphthalene, 1-bromo-4-ethoxy-

CCOc1ccc(c2c1cccc2)Br Request for Quotation
Chemical Name: Naphthalene, 1-bromo-4-ethoxy-
CAS Number: 20900-22-5
Product Number: AG00C49Y(AGN-PC-034ESG)
Synonyms:
MDL No:
Molecular Formula: C12H11BrO
Molecular Weight: 251.1191

Identification/Properties

Computed Properties
Molecular Weight:
251.123g/mol
XLogP3:
4.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
249.999g/mol
Monoisotopic Mass:
249.999g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
183
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Bromo-4-ethoxynaphthalene is a versatile chemical compound that finds wide applications in chemical synthesis. This compound serves as a valuable building block in organic chemistry, particularly in the field of heterocyclic synthesis. Its unique structure and reactivity make it a valuable intermediate for the preparation of various functionalized naphthalene derivatives.In chemical synthesis, 1-Bromo-4-ethoxynaphthalene can be used in the preparation of biologically active compounds, pharmaceuticals, and agrochemicals. Its bromo group can undergo various substitution reactions, leading to the introduction of diverse functional groups into the naphthalene ring system. This versatility allows for the modification of the compound's properties and tailoring it to specific applications.Additionally, 1-Bromo-4-ethoxynaphthalene can participate in cross-coupling reactions, such as Suzuki-Miyaura and Negishi couplings, to form more complex organic molecules. These transformations enable the synthesis of intricate molecular structures with high efficiency and precision.Overall, the use of 1-Bromo-4-ethoxynaphthalene in chemical synthesis exemplifies its significance as a valuable tool for organic chemists aiming to construct intricate molecules with tailored properties for various industrial and research applications.