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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-Alloisoleucine, N-[(phenylmethoxy)carbonyl]-

CC[C@@H]([C@H](C(=O)O)NC(=O)OCc1ccccc1)C Request for Quotation
Chemical Name: D-Alloisoleucine, N-[(phenylmethoxy)carbonyl]-
CAS Number: 55723-45-0
Product Number: AG00I9XU(AGN-PC-0OC9CH)
Synonyms:
MDL No: MFCD02094394
Molecular Formula: C14H19NO4
Molecular Weight: 265.3050

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
265.309g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
265.131g/mol
Monoisotopic Mass:
265.131g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
300
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Cbz-D-allo-isoleucine, also known as N-carbobenzyloxy-D-allo-isoleucine, is a valuable compound used in chemical synthesis for the creation of peptide and protein derivatives. Its unique structure and properties make it an important building block in the development of pharmaceuticals, particularly in the field of peptide chemistry.As a protected amino acid derivative, Cbz-D-allo-isoleucine serves as a key intermediate in the synthesis of complex peptides and proteins. Its carbobenzyloxy (Cbz) group provides protection for the amino group, enabling selective reactions at other functional groups within the molecule. This protection strategy is crucial in peptide synthesis to prevent unwanted side reactions and ensure regioselectivity during the coupling of amino acids.In addition, the D-allo stereochemistry of Cbz-D-allo-isoleucine imparts specific conformational properties to the resulting peptides, influencing their biological activity and stability. This is particularly important in the design of peptide-based therapeutics, where the stereochemistry of amino acids plays a critical role in determining the efficacy and selectivity of the final drug candidate.Overall, the application of Cbz-D-allo-isoleucine in chemical synthesis facilitates the efficient and controlled construction of peptide and protein analogs with tailored structures and functions. Its versatility and compatibility with solid-phase peptide synthesis methods make it a valuable tool for researchers and pharmaceutical scientists seeking to develop novel peptide-based compounds for various applications.