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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)-

Glycine-d5

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Chemical Name: Glycine-d5
CAS Number: 4896-77-9
Product Number: AG00I8TP(AGN-PC-0S1A0S)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
80.098g/mol
XLogP3:
-3.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
80.063g/mol
Monoisotopic Mass:
80.063g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
5
Formal Charge:
0
Complexity:
42.9
Isotope Atom Count:
5
Defined Atom Stereocenter Count:
0
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Glycine-d5 is a deuterium-labeled form of the amino acid glycine, where the five hydrogens in the methyl group are replaced with deuterium atoms. This isotopically labeled compound is widely used in chemical synthesis for a variety of applications. In organic chemistry, Glycine-d5 serves as a stable and inert isotopic tracer, allowing for precise tracking of chemical reactions and elucidation of reaction mechanisms. Due to its unique isotopic composition, Glycine-d5 can be used in NMR spectroscopy to study metabolic pathways, protein structures, and drug interactions. It is a valuable tool in pharmaceutical research, biochemical studies, and isotopic labeling experiments. Furthermore, Glycine-d5 can be employed in the synthesis of labeled peptides and proteins for fundamental research and drug development purposes. Its versatility and utility make Glycine-d5 an essential component in the repertoire of chemists and researchers seeking to explore the intricate world of chemical reactions and biomolecular interactions.