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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)-

L-Cysteine, S-2-propynyl-

N[C@H](C(=O)O)CSCC#C Request for Quotation
Chemical Name: L-Cysteine, S-2-propynyl-
CAS Number: 3262-64-4
Product Number: AG003C8T(AGN-PC-0O8XPJ)
Synonyms:
MDL No:
Molecular Formula: C6H9NO2S
Molecular Weight: 159.2062

Identification/Properties

Properties
MP:
176-178℃ (decomp)
BP:
294.8°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
159.203g/mol
XLogP3:
-2.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
159.035g/mol
Monoisotopic Mass:
159.035g/mol
Topological Polar Surface Area:
88.6A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
160
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-2-Amino-3-(prop-2-yn-1-ylthio)propanoic acid is a versatile compound widely utilized in chemical synthesis. Its unique structure, featuring an amino group and a propynylthio group, allows for its application in several key reactions. One prominent use of this compound is as a chiral building block in the synthesis of pharmaceuticals and agrochemicals. Its chiral nature plays a crucial role in controlling the stereochemistry of the target molecules during the synthesis process, ensuring the desired enantiomeric purity. Additionally, (R)-2-Amino-3-(prop-2-yn-1-ylthio)propanoic acid can serve as a ligand in metal-catalyzed reactions, facilitating various transformations through coordination to transition metals. This compound's versatility and reactivity make it a valuable tool for chemists seeking to access complex molecules efficiently and with high stereocontrol.