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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 3-(1-aminoethyl)benzoate hydrochloride

COC(=O)c1cccc(c1)[C@H](N)C.Cl Request for Quotation
Chemical Name: (R)-Methyl 3-(1-aminoethyl)benzoate hydrochloride
CAS Number: 1236353-78-8
Product Number: AG000KWP(AGN-PC-0WAMJ9)
Synonyms:
MDL No: MFCD12910778
Molecular Formula: C10H14ClNO2
Molecular Weight: 215.6767

Identification/Properties

Computed Properties
Molecular Weight:
215.677g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
215.071g/mol
Monoisotopic Mass:
215.071g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
182
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-Methyl 3-(1-aminoethyl)benzoate hydrochloride is a versatile compound widely used in chemical synthesis processes. Its application in the field of chemistry involves serving as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials.This compound plays a crucial role as a chiral intermediate in the synthesis of biologically active molecules, enabling the creation of enantiopure compounds with high levels of stereochemical purity. Its unique structure allows for precise control over the stereochemistry of the final product, making it highly valuable in the development of new drugs and other complex molecules.In addition, (R)-Methyl 3-(1-aminoethyl)benzoate hydrochloride can be utilized in asymmetric catalysis, where it acts as a chiral ligand or catalyst to facilitate enantioselective reactions. This compound's ability to induce chirality in the molecules being synthesized is particularly important in the pharmaceutical industry, where the activity and safety of drugs often depend on the specific arrangement of atoms in the molecule.Overall, (R)-Methyl 3-(1-aminoethyl)benzoate hydrochloride is a critical component in chemical synthesis, enabling chemists to create complex molecules with precise stereochemical control and opening up new possibilities for the development of innovative products in various fields.