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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-Serine, O-(1,1-dimethylethyl)-N-[(phenylmethoxy)carbonyl]-, methylester

COC(=O)[C@@H](NC(=O)OCc1ccccc1)COC(C)(C)C Request for Quotation
Chemical Name: L-Serine, O-(1,1-dimethylethyl)-N-[(phenylmethoxy)carbonyl]-, methylester
CAS Number: 1872-59-9
Product Number: AG003TI5(AGN-PC-0QGDHJ)
Synonyms:
MDL No:
Molecular Formula: C16H23NO5
Molecular Weight: 309.3575

Identification/Properties

Properties
MP:
43 °C
BP:
437.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
309.362g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
9
Exact Mass:
309.158g/mol
Monoisotopic Mass:
309.158g/mol
Topological Polar Surface Area:
73.9A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
358
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-Methyl 2-(((benzyloxy)carbonyl)amino)-3-(tert-butoxy)propanoate is a versatile compound that plays a crucial role in chemical synthesis. This compound is utilized as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structural properties make it an essential substrate for the formation of complex molecules through various synthetic pathways, including esterification, amidation, and selective deprotection reactions. By harnessing the reactivity of (S)-Methyl 2-(((benzyloxy)carbonyl)amino)-3-(tert-butoxy)propanoate, chemists can access an array of structurally diverse compounds with potential applications in drug discovery and material science. With its strategic position in chemical synthesis, this compound enables the efficient construction of molecular architectures with precise stereochemical control, paving the way for the development of innovative compounds with enhanced biological activities and physical properties.