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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)-

Acetamide-15N

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Chemical Name: Acetamide-15N
CAS Number: 1449-72-5
Product Number: AG00ACRG(AGN-PC-0PWEV9)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
60.061g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
60.034g/mol
Monoisotopic Mass:
60.034g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
4
Formal Charge:
0
Complexity:
33
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


Acetamide-^15N is a valuable tool in chemical synthesis due to its unique isotopic composition, which incorporates a nitrogen-15 isotope into the acetamide molecule. This isotopic labeling allows for precise tracking and identification of reaction products in a variety of chemical processes. In organic synthesis, Acetamide-^15N can be used as a stable isotopic marker to study reaction mechanisms, intermediate species formation, and product distribution. Its application extends to pharmaceutical research, where isotopic labeling is essential for drug development and efficacy studies. The incorporation of Acetamide-^15N provides a powerful analytical technique to elucidate complex molecular pathways and improve the efficiency and accuracy of chemical synthesis strategies.