Hexanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-methyl-, (4R)-


Chemical Name: Hexanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-methyl-, (4R)-
CAS Number: 197006-14-7
Product Number: AG007R2W(AGN-PC-0O6O7E)
Synonyms:
MDL No: MFCD02094562
Molecular Formula: C12H23NO4
Molecular Weight: 245.3153

Identification/Properties


Computed Properties
Molecular Weight:
245.319g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
245.163g/mol
Monoisotopic Mass:
245.163g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
268
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



(R)-Boc-4-amino-5-methylhexanoic acid is a versatile compound widely utilized in chemical synthesis, particularly in the field of peptide synthesis. As a key building block, it serves as a crucial intermediate in the creation of peptides with specific sequences and properties. In the process of solid-phase peptide synthesis, this compound acts as a protected amino acid, facilitating the controlled addition of subsequent amino acids to construct peptide chains. Its Boc (tert-butyloxycarbonyl) protecting group ensures selective reactivity and aids in preventing unwanted side reactions, thus enabling the precise formation of peptide bonds. This compound's strategic incorporation into peptide structures contributes to the development of bioactive peptides, pharmaceuticals, and materials with tailored functions and characteristics.