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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, [1-(hydroxymethyl)-3-(methylthio)propyl]-,1,1-dimethylethyl ester, (S)-

CSCC[C@H](NC(=O)OC(C)(C)C)CO Request for Quotation
Chemical Name: Carbamic acid, [1-(hydroxymethyl)-3-(methylthio)propyl]-,1,1-dimethylethyl ester, (S)-
CAS Number: 51372-93-1
Product Number: AG003SFG(AGN-PC-0SACHP)
Synonyms:
MDL No:
Molecular Formula: C10H21NO3S
Molecular Weight: 235.3436

Identification/Properties

Properties
MP:
48.0 to 52.0 °C
BP:
370.868°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
235.342g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
235.124g/mol
Monoisotopic Mass:
235.124g/mol
Topological Polar Surface Area:
83.9A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
192
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:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P301+P310
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Boc-Methioninol is a valuable compound used in chemical synthesis for the protection of amino groups. This compound functions as a versatile protecting group, specifically for the amino group of methionine residues in peptide synthesis. By selectively blocking the amino group with the Boc (tert-butyloxycarbonyl) moiety, Boc-Methioninol helps prevent unwanted side reactions during the synthesis of peptides.In peptide chemistry, the strategic protection of functional groups is crucial to control the sequence of reactions and avoid unwanted interactions. Boc-Methioninol plays a pivotal role in this regard by temporarily masking the amino group of methionine, thus allowing other reactions to occur selectively at desired locations within the peptide chain. This protection strategy enables chemists to synthesize complex peptides with high purity and efficiency.Furthermore, the Boc group can be easily removed under mild acidic conditions, leading to the deprotection of the amino group and the regeneration of the free methionine residue. This feature adds to the versatility of Boc-Methioninol in peptide synthesis, as it allows for the controlled manipulation of amino groups throughout the synthetic process.Overall, Boc-Methioninol serves as a valuable tool in chemical synthesis, particularly in peptide chemistry, where precise control over functional group protection is essential for the successful assembly of complex peptide structures.