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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)-

D-Serine, N-[(1,1-dimethylethoxy)carbonyl]-, phenylmethyl ester

OC[C@H](C(=O)OCc1ccccc1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: D-Serine, N-[(1,1-dimethylethoxy)carbonyl]-, phenylmethyl ester
CAS Number: 141527-78-8
Product Number: AG001GK1(AGN-PC-0O27VH)
Synonyms:
MDL No:
Molecular Formula: C15H21NO5
Molecular Weight: 295.3309

Identification/Properties

Properties
MP:
66-70℃
BP:
458.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
295.335g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
8
Exact Mass:
295.142g/mol
Monoisotopic Mass:
295.142g/mol
Topological Polar Surface Area:
84.9A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
345
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


Boc-D-Ser-OBzl, or N-tert-Butoxycarbonyl-D-serine benzyl ester, is a valuable compound widely used in chemical synthesis. This compound serves as a key building block in peptide synthesis, particularly in the production of peptides with D-amino acids. The Boc (tert-butoxycarbonyl) protecting group ensures the selectivity of the reaction by blocking unwanted side reactions, thus allowing for precise control over the peptide chain assembly. Additionally, the benzyl ester group provides stability during the synthesis process and can be easily removed under mild conditions to reveal the desired peptide sequence. Boc-D-Ser-OBzl is essential for the creation of custom peptides for research purposes, pharmaceutical development, and biochemical studies. Its versatility and reliability make it a crucial component in the toolbox of synthetic chemists striving to produce complex peptides with high purity and efficiency.