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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)-

1-(3-chlorophenyl)ethanol

Clc1cccc(c1)[C@H](O)C Request for Quotation
Chemical Name: 1-(3-chlorophenyl)ethanol
CAS Number: 120121-01-9
Product Number: AG000QD0(AGN-PC-0JM2P0)
Synonyms:
MDL No:
Molecular Formula: C8H9ClO
Molecular Weight: 156.6095

Identification/Properties

Computed Properties
Molecular Weight:
156.609g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
156.034g/mol
Monoisotopic Mass:
156.034g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
105
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 (R)-1-(3-Chlorophenyl)ethanol is a versatile compound widely used in chemical synthesis as a chiral building block. Its unique stereochemistry allows for the creation of complex organic molecules with specific chirality, making it a valuable tool in the pharmaceutical and fine chemical industries. This compound can serve as a precursor for the synthesis of various pharmaceutical agents, agrochemicals, and advanced materials through the introduction of functional groups or transformation into other chiral intermediates. Its application in asymmetric synthesis, catalysis, and medicinal chemistry highlights its significance in the development of novel compounds with enhanced biological activity and selectivity.