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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)-

Butanoic acid, 2-naphthalenyl ester

CCCC(=O)Oc1ccc2c(c1)cccc2 Request for Quotation
Chemical Name: Butanoic acid, 2-naphthalenyl ester
CAS Number: 5856-33-7
Product Number: AG00E9HI(AGN-PC-0JMIMH)
Synonyms:
MDL No:
Molecular Formula: C14H14O2
Molecular Weight: 214.2598

Identification/Properties

Properties
BP:
338.1°C at 760 mmHg
Storage:
Keep in dry area;-10 ℃;
Computed Properties
Molecular Weight:
214.264g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
214.099g/mol
Monoisotopic Mass:
214.099g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
237
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


Naphthalen-2-yl butyrate, also known as 2-naphthyl butyrate, is a versatile compound that finds application in various chemical synthesis processes. This compound is commonly used as a precursor for the synthesis of organic molecules with potential pharmaceutical and agrochemical applications.One key application of Naphthalen-2-yl butyrate is its role as a building block in the synthesis of heterocyclic compounds. By incorporating this compound into chemical reactions, chemists can access a diverse range of heterocycles with unique properties and functionalities. These heterocycles serve as important intermediates in the preparation of bioactive molecules and advanced materials.Furthermore, Naphthalen-2-yl butyrate can be utilized in the synthesis of chiral molecules. Its structural features enable chemists to introduce chirality into target molecules, facilitating the creation of enantiopure compounds with potential biological activity or functional properties.Overall, the strategic use of Naphthalen-2-yl butyrate in chemical synthesis allows for the efficient construction of complex molecules with tailored properties, making it a valuable tool in the development of new materials and bioactive compounds.