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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-Naphthaleneacetic acid, a-amino-, (S)-

OC(=O)[C@H](c1ccc2c(c1)cccc2)N Request for Quotation
Chemical Name: 2-Naphthaleneacetic acid, a-amino-, (S)-
CAS Number: 93779-35-2
Product Number: AG0060VZ(AGN-PC-0W3DT5)
Synonyms:
MDL No:
Molecular Formula: C12H11NO2
Molecular Weight: 201.2212

Identification/Properties

Properties
BP:
398°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-2-Amino-2-(naphthalen-2-yl)acetic acid, also known as $name$, is a valuable compound widely utilized in chemical synthesis. This compound plays a crucial role as a chiral building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure, incorporating a naphthalene ring and an amino acid functionality, makes it a versatile intermediate for the synthesis of complex molecules with specific stereochemical properties.In organic synthesis, (S)-2-Amino-2-(naphthalen-2-yl)acetic acid is commonly employed as a starting material for the preparation of biologically active compounds such as drugs and natural products. Its chiral nature allows chemists to control the stereochemistry of the final products, enabling the production of enantiomerically pure molecules with enhanced biological activity and reduced side effects. Additionally, the presence of the naphthalene moiety in the molecule imparts unique physicochemical properties that are advantageous in drug design and discovery.Overall, (S)-2-Amino-2-(naphthalen-2-yl)acetic acid serves as a valuable tool for organic chemists seeking to access diverse molecular architectures with precise stereochemical control. Its application in chemical synthesis opens up avenues for the development of novel compounds with potential therapeutic or industrial significance.