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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-Propanol, 1-methoxy-, (2R)-

COC[C@H](O)C Request for Quotation
Chemical Name: 2-Propanol, 1-methoxy-, (2R)-
CAS Number: 4984-22-9
Product Number: AG0038PC(AGN-PC-0OB308)
Synonyms:
MDL No:
Molecular Formula: C4H10O2
Molecular Weight: 90.1210

Identification/Properties

Computed Properties
Molecular Weight:
90.122g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
90.068g/mol
Monoisotopic Mass:
90.068g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
28.7
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


The chiral compound (R)-(-)-1-Methoxy-2-propanol, also known as (R)-MP, plays a crucial role in chemical synthesis as a versatile building block for creating a wide range of advanced materials. Its chirality, stemming from the asymmetric carbon atom, imparts unique properties that enable its application in various chemical transformations and reactions. In the realm of organic synthesis, (R)-(-)-1-Methoxy-2-propanol serves as a valuable reagent for the preparation of enantiopure compounds, making it particularly useful in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its presence can facilitate the formation of complex molecular structures with high selectivity and efficiency, enhancing the overall yield and purity of the desired products. Additionally, (R)-(-)-1-Methoxy-2-propanol can act as a solvent or a chiral auxiliary in asymmetric synthesis, enabling the synthesis of optically active molecules with specific stereochemical properties. Its ability to control the stereochemistry of reactions makes it a valuable tool for chemists seeking to access enantiomerically pure compounds for various applications in industry and academia.