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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, N-acetyl-S-(3,4-dihydroxybutyl)-

OCC(CCSC[C@@H](C(=O)O)NC(=O)C)O Request for Quotation
Chemical Name: L-Cysteine, N-acetyl-S-(3,4-dihydroxybutyl)-
CAS Number: 144889-50-9
Product Number: AG001KAL(AGN-PC-0O2Z65)
Synonyms:
MDL No:
Molecular Formula: C9H17NO5S
Molecular Weight: 251.3000

Identification/Properties

Computed Properties
Molecular Weight:
251.297g/mol
XLogP3:
-1.1
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
251.083g/mol
Monoisotopic Mass:
251.083g/mol
Topological Polar Surface Area:
132A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
236
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
1
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


L-Cysteine, N-acetyl-S-(3,4-dihydroxybutyl)- is a valuable compound utilized in chemical synthesis for its role as a versatile building block in a variety of reactions. With its unique structure and functional groups, this compound serves as a crucial intermediate in the creation of various complex molecules in the pharmaceutical, agrochemical, and materials science industries.The presence of the acetyl and hydroxybutyl groups in L-Cysteine, N-acetyl-S-(3,4-dihydroxybutyl)- enables it to participate in key chemical transformations such as acylation, alkylation, and condensation reactions. These reactions play a vital role in the preparation of pharmaceutical compounds, where precise functional group manipulation is essential for the development of advanced drug candidates.Furthermore, L-Cysteine, N-acetyl-S-(3,4-dihydroxybutyl)- is also utilized in the synthesis of specialty chemicals and materials with specific properties. Its ability to act as a linker or a modifier in molecular design processes allows for the creation of tailored molecules with enhanced functionalities, making it a valuable tool in the field of chemical synthesis.