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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)-

L-Alanine, N-benzoyl-

CC(C(=O)O)NC(=O)c1ccccc1 Request for Quotation
Chemical Name: L-Alanine, N-benzoyl-
CAS Number: 1205-02-3
Product Number: AG003SQP(AGN-PC-0O05DT)
Synonyms:
MDL No:
Molecular Formula: C10H11NO3
Molecular Weight: 193.1992

Identification/Properties

Properties
MP:
165-167 °C
BP:
452.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5300 (estimate)
Computed Properties
Molecular Weight:
193.202g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
193.074g/mol
Monoisotopic Mass:
193.074g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
221
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

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Chemical Structure


Benzoyl-DL-alanine is a versatile compound that finds widespread application in chemical synthesis. Its unique structure and properties make it a valuable reagent in various organic reactions. This compound is commonly used as a chiral building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Benzoyl-DL-alanine is particularly useful in asymmetric synthesis, where its chirality can be leveraged to create enantiomerically pure compounds. Additionally, it can serve as a precursor for the preparation of complex molecules with specific stereochemistries. Its role in chemical synthesis highlights its significance as a key intermediate in the production of diverse compounds with tailored structures and functions.