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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-chloro-, (2R)-

C[C@H](CCl)O Request for Quotation
Chemical Name: 2-Propanol, 1-chloro-, (2R)-
CAS Number: 19141-39-0
Product Number: AG002F7I(AGN-PC-0O65WE)
Synonyms:
MDL No:
Molecular Formula: C3H7ClO
Molecular Weight: 94.5401

Identification/Properties

Properties
BP:
126°C
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
94.538g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
94.019g/mol
Monoisotopic Mass:
94.019g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
5
Formal Charge:
0
Complexity:
22.9
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-1-Chloropropan-2-ol, also known as (R)-1-chloro-2-propanol, is a valuable compound with significant applications in chemical synthesis. As an enantiomerically pure form of 1-chloropropan-2-ol, this compound plays a crucial role in producing chiral molecules with specific stereochemistry, making it a useful building block in asymmetric synthesis. Its chiral nature allows for precise control over the spatial arrangement of atoms in the molecules being synthesized, leading to the creation of complex organic compounds with high levels of stereochemical purity. In chemical synthesis, (R)-1-Chloropropan-2-ol serves as a key intermediate for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals that require chirality for their biological activity or functional properties. By incorporating this compound into synthetic routes, chemists can efficiently access enantiomerically pure products that exhibit enhanced selectivity and potency in their intended applications. Additionally, (R)-1-Chloropropan-2-ol can participate in reactions such as nucleophilic substitution, acylation, and redox processes to introduce its chirality into target molecules, enabling the development of diverse chemical structures with tailored stereochemical properties.