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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, 7-hydroxy-, methyl ester

COC(=O)c1ccc2c(c1)cc(cc2)O Request for Quotation
Chemical Name: 2-Naphthalenecarboxylic acid, 7-hydroxy-, methyl ester
CAS Number: 95901-05-6
Product Number: AG00IJID(AGN-PC-0MYFW1)
Synonyms:
MDL No:
Molecular Formula: C12H10O3
Molecular Weight: 202.2060

Identification/Properties

Computed Properties
Molecular Weight:
202.209g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
202.063g/mol
Monoisotopic Mass:
202.063g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
239
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:
H302-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


Methyl 7-hydroxy-2-naphthoate is a versatile compound commonly used in chemical synthesis. Its unique structure and functional groups make it valuable for various applications in organic chemistry.One significant use of Methyl 7-hydroxy-2-naphthoate is as a building block in the synthesis of complex organic molecules. Its hydroxyl group and naphthalene ring provide opportunities for selective functionalization and derivatization, allowing chemists to introduce desired chemical moieties at specific positions.In organic synthesis, Methyl 7-hydroxy-2-naphthoate can serve as a key intermediate for the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its presence in a synthesis pathway can enable the creation of new compounds with tailored properties and functions.Furthermore, this compound can participate in various chemical reactions such as esterification, acylation, and nucleophilic substitution, expanding its utility in the design and construction of complex molecular structures.Overall, Methyl 7-hydroxy-2-naphthoate plays a crucial role in chemical synthesis by offering a versatile platform for the creation of diverse organic compounds with applications spanning different industries.