16830-14-1 Usage
Uses
Used in Organic Synthesis:
N-NITROSO-N-ISOPROPYLUREA is used as a synthetic building block for the creation of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable asset in the development of new molecules and materials.
Used in Pharmaceutical Industry:
N-NITROSO-N-ISOPROPYLUREA is used as an intermediate in the synthesis of pharmaceutical compounds. Its ability to react with other molecules and form new chemical entities makes it a useful tool in the development of drugs with specific therapeutic properties.
Used in Chemical Research:
N-NITROSO-N-ISOPROPYLUREA is used as a research compound in the field of chemistry. It can be employed to study various reaction mechanisms, explore new synthetic pathways, and investigate the properties of related compounds.
Safety Profile
Questionable carcinogen withexperimental carcinogenic data. Mutation data reported.When heated to decomposition it emits toxic fumes ofNOx.
Check Digit Verification of cas no
The CAS Registry Mumber 16830-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,3 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16830-14:
(7*1)+(6*6)+(5*8)+(4*3)+(3*0)+(2*1)+(1*4)=101
101 % 10 = 1
So 16830-14-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H9N3O2/c1-3(2)7(6-9)4(5)8/h3H,1-2H3,(H2,5,8)
16830-14-1Relevant academic research and scientific papers
Conformational Preferences in Alkylnitrosoureas
Snyder, John K.,Stock, Leon M.
, p. 886 - 891 (2007/10/02)
The spectroscopic properties of several N-alkyl-N-nitrosoureas, N,N'-dialkyl-N-nitrosoureas, and N,N',N'-trialkyl-N-nitrosoureas have been studied in carbon disulfide and chloroform solutions.The NH stretching frequencies in the IR spectra have been observed in both concentrated and dilute solution and in the presence of added dioxane.The results indicate that there is a strong intramolecular hydrogen bond in the mono- and dialkylnitrosoureas.The chemical shifts and line widths of the NMR spectra have also been studied in these solvents.The large chemical shift differences, about 1.3 ppm, for the NH protons in the monoalkylnitrosoureas and other spectroscopic features in the monoalkyl- and dialkylnitrosoureas also indicate that an intramolecular hydrogen bond contributes to a strong conformational preference.The temperature dependence of the NMR spectra of several N,N',N'-trialkyl-N-nitrosoureas establishes that the energy barrier for rotation about the carbon dialkylamide bond is about 13 kcal mol-1.Dipolar resonance interactions are primarily responsible for this barrier.This interaction is augmented by a strong, 8-10 kcal mol-1, hydrogen bond in the mono- and dialkylnitrosoureas.
