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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-Naphthalenepropanoic acid

OC(=O)CCc1ccc2c(c1)cccc2 Request for Quotation
Chemical Name: 2-Naphthalenepropanoic acid
CAS Number: 21658-35-5
Product Number: AG003I19(AGN-PC-0JOEA8)
Synonyms:
MDL No: MFCD00092742
Molecular Formula: C13H12O2
Molecular Weight: 200.2332

Identification/Properties

Properties
BP:
382.3±11.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
200.237g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
200.084g/mol
Monoisotopic Mass:
200.084g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
225
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


3-(2-Naphthyl)propanoic acid, also known as α-naphthylpropionic acid, is a versatile compound widely used in chemical synthesis. This compound serves as a key intermediate in the production of various pharmaceuticals and organic compounds. Its unique molecular structure allows for the introduction of functional groups and modifications that are crucial in the development of novel drugs and materials.In chemical synthesis, 3-(2-Naphthyl)propanoic acid is often utilized as a building block for the preparation of different derivatives with specific properties. One common application is in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs) such as naproxen. By undergoing various transformations and reactions, this compound can be converted into pharmaceutically active molecules that exhibit analgesic and anti-inflammatory properties.Furthermore, 3-(2-Naphthyl)propanoic acid plays a significant role in the development of chiral compounds due to its chiral center. Through asymmetric synthesis techniques, enantiomerically pure forms of this compound can be obtained, which are crucial in the pharmaceutical industry for the production of optically active drugs.Overall, the application of 3-(2-Naphthyl)propanoic acid in chemical synthesis is fundamental in the creation of diverse compounds with therapeutic potential and structural complexity. Its versatility and reactivity make it a valuable tool in the hands of synthetic chemists aiming to innovate and advance in the field of organic chemistry.