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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-2-hydroxy-5-methyl-, [S-(R*,R*)]-

N[C@H]([C@@H](C(=O)O)O)CC(C)C Request for Quotation
Chemical Name: Hexanoic acid, 3-amino-2-hydroxy-5-methyl-, [S-(R*,R*)]-
CAS Number: 73397-20-3
Product Number: AG005EEE(AGN-PC-0U31QP)
Synonyms:
MDL No:
Molecular Formula: C7H15NO3
Molecular Weight: 161.1989

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
161.201g/mol
XLogP3:
-2.3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
161.105g/mol
Monoisotopic Mass:
161.105g/mol
Topological Polar Surface Area:
83.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2S,3S)-3-Amino-2-hydroxy-5-methylhexanoic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis processes. This compound plays a crucial role as a chiral building block due to its unique stereochemistry. In chemical synthesis, (2S,3S)-3-Amino-2-hydroxy-5-methylhexanoic acid is often employed in the creation of complex organic molecules and pharmaceutical intermediates.Its chiral nature allows for the selective formation of specific molecular arrangements, making it valuable in the production of enantiopure compounds. By utilizing (2S,3S)-3-Amino-2-hydroxy-5-methylhexanoic acid as a starting material, chemists can control the stereochemistry of the final product, leading to the creation of compounds with desired biological activities or functional properties.Furthermore, (2S,3S)-3-Amino-2-hydroxy-5-methylhexanoic acid can act as a key component in the synthesis of peptides and peptide mimetics, enabling the construction of peptide chains with precise structural characteristics. Its presence in the synthetic pathway ensures the stereochemical integrity of the final peptide product, crucial for its biological activity and therapeutic potential.Overall, (2S,3S)-3-Amino-2-hydroxy-5-methylhexanoic acid is a valuable tool in chemical synthesis due to its chiral attributes and ability to control molecular arrangements. Its applications span across various sectors including pharmaceuticals, materials science, and agrochemicals, highlighting its significance in advancing the field of organic chemistry.