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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-(3,4-dichlorophenyl)ethanol

OC[C@@H](c1ccc(c(c1)Cl)Cl)N Request for Quotation
Chemical Name: (R)-2-Amino-2-(3,4-dichlorophenyl)ethanol
CAS Number: 1213008-01-5
Product Number: AG009G6J(AGN-PC-0WB00H)
Synonyms:
MDL No: MFCD09253679
Molecular Formula: C8H9Cl2NO
Molecular Weight: 206.0692

Identification/Properties

Computed Properties
Molecular Weight:
206.066g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
205.006g/mol
Monoisotopic Mass:
205.006g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
145
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:
H302-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-(3,4-dichlorophenyl)ethanol, commonly known as $name$, serves as a valuable intermediate in chemical synthesis processes. This compound plays a crucial role in organic chemistry as a chiral building block, particularly in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and properties make it a versatile reagent for the creation of complex molecular structures with high stereochemical purity. Utilized in asymmetric synthesis, $name$ enables the selective formation of enantiomerically pure compounds, essential for drug discovery and development efforts. This compound's application extends to the creation of novel materials, catalysts, and biologically active molecules, highlighting its significance in advancing modern synthetic chemistry methodologies.