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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-(aminocarbonyl)-3-methylbutyl]-, phenylmethyl ester,(S)-

CC(C[C@@H](C(=O)N)NC(=O)OCc1ccccc1)C Request for Quotation
Chemical Name: Carbamic acid, [1-(aminocarbonyl)-3-methylbutyl]-, phenylmethyl ester,(S)-
CAS Number: 4801-79-0
Product Number: AG00DCFO(AGN-PC-0RY46A)
Synonyms:
MDL No:
Molecular Formula: C14H20N2O3
Molecular Weight: 264.3202

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
264.325g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
7
Exact Mass:
264.147g/mol
Monoisotopic Mass:
264.147g/mol
Topological Polar Surface Area:
81.4A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
299
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:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-Benzyl (1-amino-4-methyl-1-oxopentan-2-yl)carbamate, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role as a chiral building block in organic chemistry, specifically in the synthesis of pharmaceuticals and agrochemicals. The unique structural properties of (S)-Benzyl (1-amino-4-methyl-1-oxopentan-2-yl)carbamate make it a valuable intermediate in the creation of complex molecules with high stereochemical purity. Its distinct chirality enables precise control over the stereochemistry of the final product, making it a valuable tool for chemists working on asymmetric synthesis. Combine this compound with various reagents and catalysts to access a diverse array of enantiomerically pure compounds, essential in the development of novel drugs and biologically active molecules. In summary, (S)-Benzyl (1-amino-4-methyl-1-oxopentan-2-yl)carbamate is a key component in chemical synthesis, enabling efficient construction of intricate molecular structures with precise stereochemical control.