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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)-

DL-Isoleucine, N-[(1,1-dimethylethoxy)carbonyl]-

CC[C@@H]([C@@H](C(=O)O)NC(=O)OC(C)(C)C)C Request for Quotation
Chemical Name: DL-Isoleucine, N-[(1,1-dimethylethoxy)carbonyl]-
CAS Number: 116194-21-9
Product Number: AG000BV9(AGN-PC-0JLUCS)
Synonyms:
MDL No:
Molecular Formula: C11H21NO4
Molecular Weight: 231.2887

Identification/Properties

Computed Properties
Molecular Weight:
231.292g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
231.147g/mol
Monoisotopic Mass:
231.147g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
257
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


BOC-DL-Isoleucine is a valuable building block used in chemical synthesis for the creation of various peptides and small molecules. As a protected form of the amino acid isoleucine with a BOC (tert-butyloxycarbonyl) group attached, BOC-DL-Isoleucine offers enhanced stability and functionality during synthesis processes. This compound is widely employed in the pharmaceutical industry for the production of peptide-based drugs and bioactive compounds. By incorporating BOC-DL-Isoleucine into peptide synthesis reactions, chemists can selectively control the addition of isoleucine residues, facilitating the design and construction of complex peptide structures with precise sequences and properties. Additionally, BOC-DL-Isoleucine serves as a key component in the development of peptide libraries for drug discovery and molecular biology research. Its strategic role in chemical synthesis makes it an indispensable tool for the production of advanced peptides and pharmaceuticals.