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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)-

(S)-2-amino-2-methyl-4-pentenoicacid

C[C@@](C(=O)O)(CC=C)N Request for Quotation
Chemical Name: (S)-2-amino-2-methyl-4-pentenoicacid
CAS Number: 96886-55-4
Product Number: AG003CFB(AGN-PC-0WA2V4)
Synonyms:
MDL No:
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570

Identification/Properties

Properties
BP:
226.2 °C at 760 mmHg
Storage:
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-methylpent-4-enoic acid is an important chiral building block widely used in chemical synthesis. Its enantiopure form provides a valuable tool for asymmetric synthesis, making it a key component in the production of pharmaceuticals, agrochemicals, and other fine chemicals. This compound can serve as a precursor in the synthesis of various pharmaceutical agents, such as amino acids, peptides, and complex natural products, where stereochemistry plays a crucial role in determining their biological activity. Additionally, (S)-2-Amino-2-methylpent-4-enoic acid's unique structure allows for the creation of novel molecules with specific stereochemical properties, making it a versatile and indispensable reagent in modern organic synthesis.