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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-Pyridinemethanol, a-methyl-, (aR)-

C[C@H](c1ccccn1)O Request for Quotation
Chemical Name: 2-Pyridinemethanol, a-methyl-, (aR)-
CAS Number: 27911-63-3
Product Number: AG0032FH(AGN-PC-0R3KUJ)
Synonyms:
MDL No:
Molecular Formula: C7H9NO
Molecular Weight: 123.1525

Identification/Properties

Properties
BP:
210.6°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Refractive Index:
n20/D 1.528
Computed Properties
Molecular Weight:
123.155g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
123.068g/mol
Monoisotopic Mass:
123.068g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
85
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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


The enantiomer (R)-α-Methyl-2-pyridinemethanol is a valuable chiral building block commonly employed in various chemical synthesis processes. Its asymmetric nature makes it especially useful in the construction of complex molecules where stereochemistry plays a crucial role in determining the desired properties and functions. (R)-α-Methyl-2-pyridinemethanol is frequently utilized as a catalyst or ligand in asymmetric synthesis reactions, enabling the production of enantiomerically enriched compounds with high levels of selectivity and efficiency. This compound's versatile application in asymmetric transformations contributes significantly to the advancement of pharmaceuticals, agrochemicals, and materials science, facilitating the synthesis of biologically active compounds and functional materials with tailored properties.