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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-Glucose-1,2-13C2

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Chemical Name: D-Glucose-1,2-13C2
CAS Number: 138079-87-5
Product Number: AG0017YF(AGN-PC-0PM5GI)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
150-152℃ (lit.)
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


D-Glucose-1,2-13C2 is a versatile compound commonly used in chemical synthesis. Its unique isotopic labeling pattern makes it a valuable tool in studies involving metabolic pathways, biochemical reactions, and compound identification. This labeled glucose derivative allows researchers to track the fate of specific carbons in molecules, enabling a better understanding of complex biological processes. In organic chemistry, D-Glucose-1,2-13C2 can be employed as a tracer molecule to investigate reaction mechanisms, analyze metabolic fluxes, and study enzyme kinetics. Its application extends to fields such as pharmaceutical research, food science, and environmental studies, offering valuable insights into carbon rearrangements and molecular transformations. By incorporating D-Glucose-1,2-13C2 into synthetic pathways, scientists can elucidate intricate metabolic networks and develop novel strategies for drug development and biomolecule production.