1. Home
  2. D-Alanine, D-alanyl-

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)-

D-Alanine, D-alanyl-

C[C@H](C(=O)O)NC(=O)[C@H](N)C Request for Quotation
Chemical Name: D-Alanine, D-alanyl-
CAS Number: 923-16-0
Product Number: AG00IH2I(AGN-PC-0ON607)
Synonyms:
MDL No:
Molecular Formula: C6H12N2O3
Molecular Weight: 160.1711

Identification/Properties

Properties
BP:
402.6 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
160.173g/mol
XLogP3:
-3.3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
160.085g/mol
Monoisotopic Mass:
160.085g/mol
Topological Polar Surface Area:
92.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
169
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


D-Alanyl-D-alanine, known for its application in chemical synthesis, serves as a critical building block in the creation of certain antibiotics, particularly those that target bacterial cell walls. By incorporating D-Alanyl-D-alanine into antibiotic formulations, it disrupts the synthesis of peptidoglycan, an essential component of bacterial cell walls. This disruption ultimately leads to bacterial cell death, making D-Alanyl-D-alanine a valuable tool in combatting bacterial infections. In chemical synthesis, this compound is utilized for its role in constructing intricate peptide chains and enhancing the efficacy of antibiotic agents.