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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, N-[(1,1-dimethylethoxy)carbonyl]-, 2-propenyl ester

OC[C@@H](C(=O)OCC=C)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-, 2-propenyl ester
CAS Number: 143966-57-8
Product Number: AG001IOK(AGN-PC-0O2RIO)
Synonyms:
MDL No:
Molecular Formula: C11H19NO5
Molecular Weight: 245.2723

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
245.275g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
8
Exact Mass:
245.126g/mol
Monoisotopic Mass:
245.126g/mol
Topological Polar Surface Area:
84.9A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
282
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Allyl (tert-butoxycarbonyl)-L-serinate is a versatile compound that finds significant application in chemical synthesis. This compound is commonly used as a protecting group in peptide synthesis due to its ability to protect the amine group of serine residues. By introducing the allyl (tert-butoxycarbonyl) protecting group, the reactivity of the serine amino acid can be controlled and selectively modified during various synthetic steps.Additionally, Allyl (tert-butoxycarbonyl)-L-serinate can also serve as a precursor in the synthesis of complex molecules, where the allyl functionality can be further manipulated to introduce various chemical moieties or facilitate specific reactions. Its strategic use in chemical synthesis allows for precise control over the reaction pathways and enables the synthesis of structurally diverse compounds with high efficiency and selectivity.