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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)-

Norleucine, 5-methyl-

N[C@H](C(=O)O)CCC(C)C Request for Quotation
Chemical Name: Norleucine, 5-methyl-
CAS Number: 31872-98-7
Product Number: AG0034AW(AGN-PC-0O8V5O)
Synonyms:
MDL No:
Molecular Formula: C7H15NO2
Molecular Weight: 145.1995

Identification/Properties

Properties
MP:
254-256°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
145.202g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
145.11g/mol
Monoisotopic Mass:
145.11g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
112
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


5-Methyl-L-norleucine, also known as 2-Amino-6-methylheptanoic acid, is a versatile compound commonly used in chemical synthesis for various applications. It serves as a key building block in the creation of peptides, pharmaceuticals, and other organic molecules due to its unique structure and properties. With its amino acid backbone and methyl group substitution, 5-Methyl-L-norleucine plays a crucial role in the development of new chemical entities and drug compounds. Its involvement in peptide synthesis allows for the modification and enhancement of bioactive peptides and proteins, leading to potential breakthroughs in the pharmaceutical industry. In addition, the strategic incorporation of 5-Methyl-L-norleucine in chemical reactions enables the synthesis of complex molecules with improved drug-like properties and biological activities. This compound's synthetic versatility and structural significance make it a valuable tool in the realm of chemical synthesis, paving the way for innovative advancements in drug discovery and medicinal chemistry.