1. Home
  2. (R)-Methyl 4-(1-aminoethyl)benzoate hydrochloride

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-aminoethyl)benzoate hydrochloride

COC(=O)c1ccc(cc1)[C@H](N)C.Cl Request for Quotation
Chemical Name: (R)-Methyl 4-(1-aminoethyl)benzoate hydrochloride
CAS Number: 1097196-96-7
Product Number: AG0092BM(AGN-PC-0WAH35)
Synonyms:
MDL No:
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:
174
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The (R)-Methyl 4-(1-aminoethyl)benzoate hydrochloride is a versatile compound widely utilized in chemical synthesis processes. Its unique chemical structure allows it to be effectively employed as a chiral building block in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. By serving as a key intermediate in synthetic pathways, this compound enables the selective introduction of chirality into complex molecules, thereby facilitating the production of enantiomerically pure compounds with enhanced biological activity and specificity. In addition to its role in asymmetric synthesis, (R)-Methyl 4-(1-aminoethyl)benzoate hydrochloride can also be utilized as a ligand in catalytic reactions, contributing to the efficient and selective formation of important chemical bonds. Its versatility and utility make it an indispensable tool in the toolbox of synthetic chemists seeking to access a diverse array of chiral compounds for various applications.