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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)-

2-Butanol, 3-methyl-, (2S)-

C[C@@H](C(C)C)O Request for Quotation
Chemical Name: 2-Butanol, 3-methyl-, (2S)-
CAS Number: 1517-66-4
Product Number: AG003CH9(AGN-PC-0O4BIT)
Synonyms:
MDL No:
Molecular Formula: C5H12O
Molecular Weight: 88.1482

Identification/Properties

Properties
MP:
-51.44℃ (estimate)
Form:
Liquid
Computed Properties
Molecular Weight:
88.15g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
88.089g/mol
Monoisotopic Mass:
88.089g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
32.9
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


(2S)-3-Methylbutan-2-ol, also known as (S)-2-Methyl-3-butanol, plays a crucial role in chemical synthesis as a versatile chiral building block. This compound is valued for its stereoselective properties, allowing it to be utilized in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. (2S)-3-Methylbutan-2-ol is commonly employed as a chiral auxiliary or a resolving agent in asymmetric synthesis to generate compounds with high enantiomeric purity. Its ability to control the stereochemistry of reactions makes it a valuable tool in the production of complex molecules with specific biological activities. Additionally, (2S)-3-Methylbutan-2-ol can serve as a precursor for the preparation of other chiral compounds through functional group transformations or derivatization reactions. Its significance in chemical synthesis lies in its ability to facilitate the creation of optically pure compounds with defined stereochemistry, making it an essential component in the toolbox of synthetic chemists.