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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-Naphthalenol, benzoate

O=C(c1ccccc1)Oc1ccc2c(c1)cccc2 Request for Quotation
Chemical Name: 2-Naphthalenol, benzoate
CAS Number: 93-44-7
Product Number: AG00GRAU(AGN-PC-09TG7O)
Synonyms:
MDL No:
Molecular Formula: C17H12O2
Molecular Weight: 248.2760

Identification/Properties

Computed Properties
Molecular Weight:
248.281g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
248.084g/mol
Monoisotopic Mass:
248.084g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
306
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Naphthyl benzoate, also known as β-naphthyl benzoate, is a versatile compound commonly used in chemical synthesis as a key intermediate in various reactions. This compound is widely employed in the field of organic chemistry for the synthesis of a range of aromatic compounds and derivatives.One of the primary applications of 2-Naphthyl benzoate in chemical synthesis is its use as a precursor in the production of pharmaceutical compounds. It serves as a valuable building block in the creation of pharmaceutical agents, particularly those with aromatic structures. Through various chemical reactions, 2-Naphthyl benzoate can be transformed into more complex molecules that exhibit specific biological activities.Furthermore, 2-Naphthyl benzoate is utilized in the preparation of various organic materials such as dyes, pigments, and fragrances. Its unique chemical structure and reactivity make it a valuable starting material for the synthesis of these important industrial products. Additionally, it can be employed in the creation of specialty polymers and materials with tailored properties.Overall, the application of 2-Naphthyl benzoate in chemical synthesis plays a vital role in the preparation of diverse compounds with significant industrial and pharmaceutical value. Its versatility and utility make it a valuable compound for organic chemists and researchers alike.