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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)-

1-AMINO-2,4-IMIDAZOLIDINEDIONE-13C3

O=[13C]1[13CH2]N([13C](=O)N1)N Request for Quotation
Chemical Name: 1-AMINO-2,4-IMIDAZOLIDINEDIONE-13C3
CAS Number: 957509-31-8
Product Number: AG006B04(AGN-PC-0W5CWQ)
Synonyms:
MDL No:
Molecular Formula: C3H5N3O2
Molecular Weight: 118.0687

Identification/Properties

Properties
MP:
>155ºC (dec.)
Storage:
-10 ℃;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
118.069g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
118.048g/mol
Monoisotopic Mass:
118.048g/mol
Topological Polar Surface Area:
75.4A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
144
Isotope Atom Count:
3
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


1-Amino Hydantoin-13C3 is a versatile compound widely used in chemical synthesis for isotope labeling purposes. By incorporating this stable isotope-labeled compound into organic molecules, researchers can track the fate and transformation of specific carbon atoms within a molecule during various chemical reactions. This allows for detailed mechanistic studies in both academic and industrial settings, providing valuable insights into reaction pathways, intermediate formation, and compound stability. Additionally, the application of 1-Amino Hydantoin-13C3 in chemical synthesis enables enhanced spectroscopic analysis, such as NMR and mass spectrometry, facilitating the identification and characterization of complex molecular structures.