1. Home
  2. Naphthalene, 1-bromo-4-(bromomethyl)-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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-(bromomethyl)-

BrCc1ccc(c2c1cccc2)Br Request for Quotation
Chemical Name: Naphthalene, 1-bromo-4-(bromomethyl)-
CAS Number: 79996-99-9
Product Number: AG0032PR(AGN-PC-0NK4KD)
Synonyms:
MDL No:
Molecular Formula: C11H8Br2
Molecular Weight: 299.9892

Identification/Properties

Properties
MP:
102-105℃ (hexane )
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
299.993g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
299.897g/mol
Monoisotopic Mass:
297.899g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
170
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

Request for Quotation

Customer Feedback

Chemical Structure


1-Bromo-4-(bromomethyl)naphthalene is a versatile compound widely used in chemical synthesis due to its unique reactivity and functional groups. With its bromomethyl substituent, this compound is particularly useful in nucleophilic substitution reactions, where the bromine groups can be easily substituted with various nucleophiles to introduce new functional groups onto the naphthalene core.In organic synthesis, 1-Bromo-4-(bromomethyl)naphthalene can serve as a valuable building block for the construction of complex molecules, such as pharmaceuticals, agrochemicals, and materials. Its reactivity allows for selective functionalization at the bromine positions, enabling chemists to control the regioselectivity of the reactions. Additionally, the presence of the naphthalene core imparts aromatic properties to the compound, making it beneficial for applications where aromaticity plays a key role in the desired chemical properties.Furthermore, the bromomethyl group in 1-Bromo-4-(bromomethyl)naphthalene can undergo various transformations, such as cross-coupling reactions and radical chemistry, expanding the synthetic possibilities and enabling the synthesis of diverse molecular structures. Overall, this compound is an essential tool in the arsenal of synthetic chemists for the efficient construction of complex organic molecules with tailored properties and functionalities.