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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)-

Carbocisteine Sulfoxide (Mixture of diastereomers)

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Chemical Name: Carbocisteine Sulfoxide (Mixture of diastereomers)
CAS Number: 5439-87-2
Product Number: AG00DDLS(AGN-PC-0WBNCJ)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
195.189g/mol
XLogP3:
-4.6
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
5
Exact Mass:
195.02g/mol
Monoisotopic Mass:
195.02g/mol
Topological Polar Surface Area:
137A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
216
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


Carbocisteine Sulfoxide, a mixture of diastereomers, is a versatile compound widely used in chemical synthesis. Its application in organic chemistry primarily involves its role as a chiral auxiliary. By leveraging the unique stereochemistry of Carbocisteine Sulfoxide, chemists can induce asymmetric reactions and control the stereochemistry of the resulting products. This compound is especially valuable in the synthesis of complex natural products and pharmaceutical intermediates, where stereochemical precision is crucial. Additionally, Carbocisteine Sulfoxide's ability to participate in various types of reactions, such as oxidation and reduction processes, further expands its utility in chemical synthesis.