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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)-

Hexanoic acid, 3-amino-5-methyl-, hydrochloride, (3S)-

CC(C[C@@H](CC(=O)O)N)C.Cl Request for Quotation
Chemical Name: Hexanoic acid, 3-amino-5-methyl-, hydrochloride, (3S)-
CAS Number: 96386-92-4
Product Number: AG003R8I(AGN-PC-0OOD2R)
Synonyms:
MDL No:
Molecular Formula: C7H16ClNO2
Molecular Weight: 181.6604

Identification/Properties

Properties
BP:
249.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
181.66g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
181.087g/mol
Monoisotopic Mass:
181.087g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
11
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


H-β-HoLeu-OH.HCl is a versatile reagent widely used in chemical synthesis for introducing the amino acid homoleucine into peptide chains. Its unique properties make it a valuable tool for peptide synthesis and drug development. With its high purity and excellent solubility, H-β-HoLeu-OH.HCl enables precise control over the synthesis process, resulting in high-quality peptides with desired properties. In addition, its compatibility with various coupling agents and protecting groups makes it a preferred choice for researchers and chemists working on peptide design and modification.