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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)-

Boc-Asp(Ochx)-OH

O=C(OC1CCCCC1)C[C@@H](C(=O)O)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: Boc-Asp(Ochx)-OH
CAS Number: 73821-95-1
Product Number: AG005KBR(AGN-PC-0WACN5)
Synonyms:
MDL No:
Molecular Formula: C15H25NO6
Molecular Weight: 315.3621

Identification/Properties

Properties
MP:
93-95 °C
BP:
487.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
315.366g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
315.168g/mol
Monoisotopic Mass:
315.168g/mol
Topological Polar Surface Area:
102A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
409
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


Boc-Asp(OcHx)-OH, also known as N-tert-butoxycarbonyl-L-aspartic acid 5-oxo-hexyl ester, is a crucial compound utilized in organic and peptide synthesis. The presence of a Boc (tert-butoxycarbonyl) protecting group on the aspartic acid residue and an OcHx (5-oxo-hexyl) ester group provide stability and enable selective manipulation of the molecule in various chemical reactions.This compound is commonly employed in peptide chemistry to introduce aspartic acid residues into peptide chains. The Boc protecting group safeguards the aspartic acid functionality during synthesis, preventing unwanted side reactions. Additionally, the OcHx ester group serves as a removable protecting group, allowing for controlled deprotection under specific reaction conditions.Overall, Boc-Asp(OcHx)-OH plays a crucial role in the efficient and precise assembly of complex peptides and organic molecules, making it an indispensable tool in chemical synthesis strategies.