1. Home
  2. Phenylalanine, a-methyl-

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)-

Phenylalanine, a-methyl-

OC(=O)C(Cc1ccccc1)(N)C Request for Quotation
Chemical Name: Phenylalanine, a-methyl-
CAS Number: 1132-26-9
Product Number: AG003GCK(AGN-PC-0P4KF8)
Synonyms:
MDL No:
Molecular Formula: C10H13NO2
Molecular Weight: 179.2157

Identification/Properties

Properties
MP:
293-294 °C (dec.)(lit.)
BP:
312.8±30.0 °C(Predicted)
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
179.219g/mol
XLogP3:
-1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
179.095g/mol
Monoisotopic Mass:
179.095g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
187
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


DL-α-Methylphenylalanine, also known as alpha-methylphenylalanine, is a valuable compound used in chemical synthesis for various applications. In organic chemistry, DL-α-Methylphenylalanine is widely utilized as a chiral building block in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique molecular structure allows for precise stereochemical control in the synthesis of complex molecules, making it a versatile tool for organic chemists. By incorporating DL-α-Methylphenylalanine into synthetic pathways, researchers can access enantiomerically pure compounds with specific biological activities or physical properties. This amino acid derivative plays a crucial role in the creation of diverse compounds, showcasing its significance in the field of chemical synthesis.