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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)-

D-Alanine, 3-amino-, monohydrochloride

N[C@@H](C(=O)O)CN.Cl Request for Quotation
Chemical Name: D-Alanine, 3-amino-, monohydrochloride
CAS Number: 6018-56-0
Product Number: AG0033LE(AGN-PC-0SV3VF)
Synonyms:
MDL No:
Molecular Formula: C3H9ClN2O2
Molecular Weight: 140.5688

Identification/Properties

Properties
MP:
240 °C
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Refractive Index:
-23 ° (C=2, 1mol/L HCl)
Computed Properties
Molecular Weight:
140.567g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
140.035g/mol
Monoisotopic Mass:
140.035g/mol
Topological Polar Surface Area:
89.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
73.3
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


3-Amino-D-Alanine Hydrochloride is a versatile compound widely utilized in chemical synthesis for several key applications. As a primary amine, it serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. When incorporated into peptide synthesis, it plays a pivotal role in the formation of peptide bonds, contributing to the development of novel protein-based therapeutics and bioactive compounds. Additionally, its chiral nature makes it an essential tool in asymmetric synthesis, enabling the production of enantiopure molecules with high stereochemical control. In the field of medicinal chemistry, 3-Amino-D-Alanine Hydrochloride is employed in the design and optimization of drug candidates, harnessing its synthetic versatility to access structurally diverse and biologically active molecules. Its significance in chemical synthesis underscores its value as a fundamental building block with widespread applications in advancing scientific research and innovation.