1. Home
  2. N-Cbz-L-Aspartic acid 4-benzyl ester

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

N-Cbz-L-Aspartic acid 4-benzyl ester

O=C(C[C@@H](C(=O)O)NC(=O)OCc1ccccc1)OCc1ccccc1 Request for Quotation
Chemical Name: N-Cbz-L-Aspartic acid 4-benzyl ester
CAS Number: 3479-47-8
Product Number: AG003SSI(AGN-PC-0WAEI8)
Synonyms:
MDL No:
Molecular Formula: C19H19NO6
Molecular Weight: 357.3573

Identification/Properties

Properties
MP:
105-107°C
BP:
587.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
357.362g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
10
Exact Mass:
357.121g/mol
Monoisotopic Mass:
357.121g/mol
Topological Polar Surface Area:
102A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
469
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

Request for Quotation

Customer Feedback

Chemical Structure


Z-Asp(OBzl)-OH, also known as Z-protected aspartic acid, is a crucial compound commonly used in chemical synthesis. With its unique chemical properties, Z-Asp(OBzl)-OH finds wide application in peptide synthesis and drug development. As a key building block in peptide chemistry, this compound serves as a versatile tool for creating specific peptide sequences with high precision and efficiency. Additionally, Z-Asp(OBzl)-OH's strategic positioning of a benzyl ester group provides protection for the aspartic acid residue, allowing for selective deprotection under controlled conditions during multi-step synthesis processes. This compound plays a pivotal role in the synthesis of complex peptides and serves as a valuable asset in the development of various pharmaceuticals and bioactive molecules.