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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)-

Cyanamide-13C

N[13C]#N Request for Quotation
Chemical Name: Cyanamide-13C
CAS Number: 21420-35-9
Product Number: AG00C2HP(AGN-PC-0QXZG4)
Synonyms:
MDL No:
Molecular Formula: CH2N2
Molecular Weight: 43.032634838

Identification/Properties

Computed Properties
Molecular Weight:
43.033g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
43.025g/mol
Monoisotopic Mass:
43.025g/mol
Topological Polar Surface Area:
49.8A^2
Heavy Atom Count:
3
Formal Charge:
0
Complexity:
29.3
Isotope Atom Count:
1
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


Cyanamide-13C, a stable isotope-labeled form of cyanamide, plays a crucial role in chemical synthesis as a versatile building block and precursor in various reactions. When incorporated into organic molecules, Cyanamide-13C can be used for isotopic labeling studies in fields such as pharmaceutical research, agrochemical development, and materials science.In synthetic chemistry, Cyanamide-13C is utilized as a labeling reagent to track the fate and transformation of specific carbon atoms within a molecule. This isotopic labeling can provide valuable insights into reaction mechanisms, product formation pathways, and compound stability under different conditions. By selectively introducing the Cyanamide-13C label at strategic positions in a molecule, researchers can elucidate the kinetics, stereochemistry, and metabolic pathways of the target compound.Moreover, Cyanamide-13C can serve as a precursor for the synthesis of various nitrogen-containing compounds, including pharmaceuticals, pesticides, and specialty chemicals. The incorporation of the isotopic label enables researchers to distinguish between different sources of nitrogen atoms in a molecule, aiding in the determination of their origins and synthetic pathways. This detailed molecular information is crucial for understanding the interactions of organic compounds in biological systems, environmental processes, and industrial applications.Overall, the application of Cyanamide-13C in chemical synthesis offers a powerful tool for studying complex organic reactions, designing new molecules with specific properties, and advancing our understanding of molecular transformations at the atomic level. Its versatility and utility make it an indispensable resource for researchers and chemists seeking to explore the intricacies of carbon and nitrogen chemistry in a wide range of scientific disciplines.