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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-(1,1-dimethylethyl)-, hydrochloride

N[C@H](C(=O)O)CSC(C)(C)C.Cl Request for Quotation
Chemical Name: L-Cysteine, S-(1,1-dimethylethyl)-, hydrochloride
CAS Number: 2481-09-6
Product Number: AG002PJ1(AGN-PC-0O881U)
Synonyms:
MDL No:
Molecular Formula: C7H16ClNO2S
Molecular Weight: 213.7254

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
213.72g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
213.059g/mol
Monoisotopic Mass:
213.059g/mol
Topological Polar Surface Area:
88.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
142
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


H-Cys(tBu)-OH.HCl, also known as Hydroxycysteine t-butyl ester hydrochloride, is a valuable chemical reagent frequently used in chemical synthesis processes. This compound serves as a versatile building block in the creation of various organic molecules and pharmaceutical intermediates. Due to its t-butyl ester group, H-Cys(tBu)-OH.HCl offers enhanced stability and solubility characteristics, making it ideal for use in a wide range of reactions such as peptide synthesis, drug development, and bioconjugation strategies. Its ability to undergo selective deprotection and functionalization reactions make it a valuable tool for synthetic chemists seeking to introduce cysteine residues into their molecules with precision and efficiency.