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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)-

2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-

Brc1ccc2c(c1)cc(c(c2Br)O)C(=O)O Request for Quotation
Chemical Name: 2-Naphthalenecarboxylic acid, 4,7-dibromo-3-hydroxy-
CAS Number: 1779-10-8
Product Number: AG003DR5(AGN-PC-0JLBNN)
Synonyms:
MDL No:
Molecular Formula: C11H6Br2O3
Molecular Weight: 345.9715

Identification/Properties

Properties
MP:
251-255 °C(lit.)
BP:
427.6°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
345.974g/mol
XLogP3:
4.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
345.866g/mol
Monoisotopic Mass:
343.868g/mol
Topological Polar Surface Area:
57.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
284
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


4,7-Dibromo-3-hydroxy-2-naphthoic acid is a versatile compound that finds wide application in chemical synthesis. One important use of this compound is as a building block in the synthesis of novel organic molecules. It serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and materials.Additionally, 4,7-Dibromo-3-hydroxy-2-naphthoic acid is commonly employed in the preparation of dyes and pigments due to its unique chemical structure and reactivity. Its functional groups allow for diverse modifications, leading to the development of a wide range of colored compounds used in various industries.Furthermore, this compound is utilized in academic research settings for its ability to undergo various chemical transformations, enabling the creation of new compounds with potential applications in drug discovery, materials science, and chemical biology. Its presence in the synthetic chemist's toolkit enables the creation of structurally complex and diverse molecules, making it a valuable resource for those working in the field of organic chemistry.