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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)-

(R)-2-Amino-2-(3-chlorophenyl)ethanol

OC[C@@H](c1cccc(c1)Cl)N Request for Quotation
Chemical Name: (R)-2-Amino-2-(3-chlorophenyl)ethanol
CAS Number: 926291-77-2
Product Number: AG0032ES(AGN-PC-0WAFQ6)
Synonyms:
MDL No:
Molecular Formula: C8H10ClNO
Molecular Weight: 171.6241

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
171.624g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
171.045g/mol
Monoisotopic Mass:
171.045g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
121
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


(R)-2-Amino-2-(3-chlorophenyl)ethanol is a valuable compound used in chemical synthesis as a chiral building block. Its specific stereochemistry and functional groups make it a versatile intermediate for the preparation of various complex molecules. In organic synthesis, this compound serves as a key starting material for the creation of pharmaceuticals, agrochemicals, and other fine chemicals. Its presence in a molecule can influence the biological activity and properties of the final product. The chiral nature of (R)-2-Amino-2-(3-chlorophenyl)ethanol allows for the creation of enantiopure compounds, which is crucial in drug development and asymmetric synthesis. This compound's application in chemical synthesis demonstrates its significance in the production of advanced materials and compounds with tailored properties and activities.