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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)-

Carbamic acid, [(1R)-1-(hydroxymethyl)-2-[(phenylmethyl)thio]ethyl]-,1,1-dimethylethyl ester

OC[C@@H](NC(=O)OC(C)(C)C)CSCc1ccccc1 Request for Quotation
Chemical Name: Carbamic acid, [(1R)-1-(hydroxymethyl)-2-[(phenylmethyl)thio]ethyl]-,1,1-dimethylethyl ester
CAS Number: 139428-96-9
Product Number: AG001B0K(AGN-PC-0POCTY)
Synonyms:
MDL No:
Molecular Formula: C15H23NO3S
Molecular Weight: 297.4130

Identification/Properties

Properties
BP:
442.9±40.0 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
297.413g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
297.14g/mol
Monoisotopic Mass:
297.14g/mol
Topological Polar Surface Area:
83.9A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
285
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


Boc-Cysteinol(Bzl), a versatile compound in chemical synthesis, serves as a crucial building block in the creation of various organic molecules. With its unique properties, Boc-Cysteinol(Bzl) is extensively utilized as a protective group for thiol functionalities. Through a series of reactions, this compound can be selectively deprotected to expose the thiol group for further manipulation. This controlled reactivity enables precise and efficient derivatization of thiol-containing compounds, facilitating the synthesis of intricate organic structures. In addition, Boc-Cysteinol(Bzl) plays a key role in the construction of peptide and protein molecules, where the protection and deprotection of thiol groups are essential for achieving specific structural configurations. Its compatibility with a wide range of synthetic methods makes Boc-Cysteinol(Bzl) a valuable tool in the synthesis of complex organic molecules with diverse applications in pharmaceuticals, materials science, and bioconjugation chemistry.