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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)-4-Amino-4-phenylbutanoic acid hydrochloride

N[C@@H](c1ccccc1)CCC(=O)O.Cl Request for Quotation
Chemical Name: (R)-4-Amino-4-phenylbutanoic acid hydrochloride
CAS Number: 1010129-08-4
Product Number: AG0003IZ(AGN-PC-0WAMCU)
Synonyms:
MDL No: MFCD12759018
Molecular Formula: C10H14ClNO2
Molecular Weight: 215.6767

Identification/Properties

Computed Properties
Molecular Weight:
215.677g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
215.071g/mol
Monoisotopic Mass:
215.071g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
164
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


Known for its vital role in chemical synthesis, (R)-4-Amino-4-phenylbutanoic acid hydrochloride is a versatile compound that serves as a key building block in the creation of various pharmaceuticals. By incorporating this compound into reaction mixtures, chemists can facilitate the formation of complex molecular structures with high efficiency and precision. Its unique chemical properties enable it to participate in a wide range of reactions, making it a valuable asset in the development of new drugs, agrochemicals, and other bioactive compounds. Additionally, (R)-4-Amino-4-phenylbutanoic acid hydrochloride offers exceptional chirality, enhancing the stereochemical control of reactions and ensuring the production of optically pure products. In the realm of chemical synthesis, this compound stands as an indispensable tool for researchers and industry professionals alike, driving innovation and advancement in the field.