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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)-Methyl 4-(1-amino-2-hydroxyethyl)benzoate hydrochloride

OC[C@@H](c1ccc(cc1)C(=O)OC)N.Cl Request for Quotation
Chemical Name: (R)-Methyl 4-(1-amino-2-hydroxyethyl)benzoate hydrochloride
CAS Number: 1196049-17-8
Product Number: AG000PA0(AGN-PC-0WAMJ5)
Synonyms:
MDL No: MFCD12910852
Molecular Formula: C10H14ClNO3
Molecular Weight: 231.6761

Identification/Properties

Computed Properties
Molecular Weight:
231.676g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
231.066g/mol
Monoisotopic Mass:
231.066g/mol
Topological Polar Surface Area:
72.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
188
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:
2
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)-Methyl 4-(1-amino-2-hydroxyethyl)benzoate hydrochloride serves as a valuable reagent in chemical synthesis processes, particularly in the field of medicinal chemistry and pharmaceutical development. This compound is adept at facilitating the construction of complex molecular structures with high levels of stereochemical control. Its unique structural features make it a versatile building block for the creation of a wide array of biologically active molecules, such as pharmaceutical intermediates and drug candidates. By harnessing the reactivity of this compound, chemists are able to carry out precision transformations that are crucial for the synthesis of new therapeutic agents and research compounds.