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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)-

Anthracene, 9-(bromomethyl)-

BrCc1c2ccccc2cc2c1cccc2 Request for Quotation
Chemical Name: Anthracene, 9-(bromomethyl)-
CAS Number: 2417-77-8
Product Number: AG0034EW(AGN-PC-0JKD7X)
Synonyms:
MDL No:
Molecular Formula: C15H11Br
Molecular Weight: 271.1518

Identification/Properties

Properties
MP:
143-146℃
BP:
411.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Refractive Index:
1.6822 (estimate)
Computed Properties
Molecular Weight:
271.157g/mol
XLogP3:
5.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
270.004g/mol
Monoisotopic Mass:
270.004g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
216
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


9-Bromomethylanthracene is a versatile compound widely used in chemical synthesis as a key building block for the creation of various organic molecules. This compound serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science. Its unique structure and reactivity make it particularly useful in the formation of complex organic frameworks. Additionally, 9-Bromomethylanthracene can participate in various organic reactions such as cross-coupling, nucleophilic substitution, and aromatic substitution, enabling chemists to access a wide range of functionalized anthracene derivatives. Its utility extends to the development of novel materials with potential applications in organic electronics, photovoltaics, and fluorescent dyes. With its importance in synthetic organic chemistry, 9-Bromomethylanthracene plays a crucial role in advancing research and discovery in the field of chemical science.