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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-Alanine, 3-[(1,1-dimethylethyl)dithio]-

N[C@H](C(=O)O)CSSC(C)(C)C Request for Quotation
Chemical Name: L-Alanine, 3-[(1,1-dimethylethyl)dithio]-
CAS Number: 30044-51-0
Product Number: AG007JUN(AGN-PC-0O8PS4)
Synonyms:
MDL No:
Molecular Formula: C7H15NO2S2
Molecular Weight: 209.3295

Identification/Properties

Computed Properties
Molecular Weight:
209.322g/mol
XLogP3:
-1.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
209.054g/mol
Monoisotopic Mass:
209.054g/mol
Topological Polar Surface Area:
114A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
156
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-2-Amino-3-(tert-butyldisulfanyl)propanoic acid offers a versatile tool in chemical synthesis applications. This compound serves as a key intermediate in the development of custom peptides and complex organic molecules. Its unique structure and properties enable precise control over stereochemistry and reactivity in various synthetic pathways. By incorporating (R)-2-Amino-3-(tert-butyldisulfanyl)propanoic acid into synthesis strategies, chemists can achieve tailored functional group transformations and strategic bond formations, facilitating the creation of novel compounds with specific biological or material properties.