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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)-

1-Naphthalenecarboxylic acid, 4-(bromomethyl)-

BrCc1ccc(c2c1cccc2)C(=O)O Request for Quotation
Chemical Name: 1-Naphthalenecarboxylic acid, 4-(bromomethyl)-
CAS Number: 30236-02-3
Product Number: AG00BCLK(AGN-PC-0NDU82)
Synonyms:
MDL No:
Molecular Formula: C12H9BrO2
Molecular Weight: 265.1027

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
265.106g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
263.979g/mol
Monoisotopic Mass:
263.979g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
242
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Bromomethyl)-1-naphthoic acid is a versatile compound widely used in organic chemical synthesis. It acts as a valuable building block in the creation of various organic molecules due to its unique structural properties. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of novel organic reactions and methodologies in the field of organic chemistry. Its bromine-containing functional group provides a site for further derivatization, enabling the creation of diverse chemical structures with specific properties and functions. By incorporating 4-(Bromomethyl)-1-naphthoic acid into chemical synthesis processes, researchers can access a wide array of potential products with applications in various industries.