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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)-

5-Hexynoic acid,3-amino-, hydrochloride (1:1), (3S)-

C#CC[C@@H](CC(=O)O)N.Cl Request for Quotation
Chemical Name: 5-Hexynoic acid,3-amino-, hydrochloride (1:1), (3S)-
CAS Number: 332064-85-4
Product Number: AG003CLU(AGN-PC-0R8QCM)
Synonyms:
MDL No:
Molecular Formula: C6H10ClNO2
Molecular Weight: 163.6021

Identification/Properties

Properties
Storage:
2-8℃;

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-3-Aminohex-5-ynoic acid hydrochloride is a valuable compound widely utilized in chemical synthesis. This compound plays a crucial role as a chiral building block in the synthesis of various pharmaceuticals and bioactive molecules. Due to its specific stereochemistry, (S)-3-Aminohex-5-ynoic acid hydrochloride is often employed in the construction of complex molecules with precise three-dimensional structures.In chemical synthesis, this compound serves as a key intermediate in the preparation of chiral ligands, pharmaceuticals, and agrochemicals. Its unique structural features make it a versatile tool for creating enantiomerically pure compounds, which are essential in the pharmaceutical industry for developing safe and effective drugs. By incorporating (S)-3-Aminohex-5-ynoic acid hydrochloride into the synthesis process, chemists can control the stereochemistry of the final product, leading to enhanced selectivity and potency.Additionally, (S)-3-Aminohex-5-ynoic acid hydrochloride can be utilized in the synthesis of functionalized amino acids, peptides, and peptidomimetics. These compounds have diverse applications in medicinal chemistry, bioconjugation, and materials science. Through innovative synthetic pathways involving (S)-3-Aminohex-5-ynoic acid hydrochloride, chemists can access a wide range of structurally complex and biologically active compounds with therapeutic potential.In summary, the application of (S)-3-Aminohex-5-ynoic acid hydrochloride in chemical synthesis opens up possibilities for creating new molecules, refining existing synthetic routes, and advancing the field of organic chemistry. Its strategic use as a chiral building block underscores its significance in modern drug discovery and molecular design.