73861
N-Nitrosodiethylamine
≥99.0% (GC)
Sinónimos:
Diethylnitrosamine
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Fórmula lineal:
(C2H5)2NNO
Número CAS:
Peso molecular:
102.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-226-1
Beilstein/REAXYS Number:
1744991
MDL number:
Assay:
≥99.0% (GC)
Form:
liquid
Servicio técnico
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Permítanos ayudarleQuality Level
assay
≥99.0% (GC)
form
liquid
IVD
for in vitro diagnostic use
bp
177 °C (lit.)
density
0.95 g/mL (lit.)
functional group
N-nitroso, amine, nitroso
SMILES string
CCN(CC)N=O
InChI
1S/C4H10N2O/c1-3-6(4-2)5-7/h3-4H2,1-2H3
InChI key
WBNQDOYYEUMPFS-UHFFFAOYSA-N
Application
N-Nitrosodiethylamine can be used as a reactant to synthesize:
- α-Amino oxime derivatives from alkenes via visible-light-induced photoaddition in the presence of HCl.
- Diethylnitrosamine metalloporphyrin complexes from metalloporphyrins in the presence of dichloromethane.
N-Nitrosodiethylamine can also be used in the synthesis of 1,1-diethylhydrazine.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Chronic 3 - Carc. 1B
Clase de almacenamiento
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Changyu Zhu et al.
Journal of hepatology, 74(3), 613-626 (2020-10-11)
The hepatocyte Notch pathway is a pathogenic factor in non-alcoholic steatohepatitis (NASH)-associated fibrosis, but its role in hepatocellular carcinoma (HCC) is less well defined. Herein, we aimed to characterize the molecular and clinical features of Notch-active human HCC, and to
Li Chen et al.
Inorganic chemistry, 37(18), 4677-4688 (2001-10-24)
Diethylnitrosamine reacts with [(TPP)Fe(THF)(2)]ClO(4) (TPP = 5,10,15,20-tetraphenylporphyrinato dianion) in toluene to generate the bis-nitrosamine complex, [(TPP)Fe(Et(2)NNO)(2)]ClO(4), in 96% isolated yield. The related [(TTP)Fe(Et(2)NNO)(2)]SbF(6) (TTP = 5,10,15,20-tetra-p-tolylporphyrinato dianion) complex is prepared in 70% isolated yield via a similar reaction in CH(2)Cl(2).
Dilip V Patil et al.
Organic letters, 23(8), 3105-3109 (2021-04-02)
The generation of aminium radical cation species from N-nitrosoamines is disclosed for the first time through visible-light excitation at 453 nm. The developed visible-light-promoted photoaddition reaction of N-nitrosoamines to alkenes was combined with the o-NQ-catalyzed aerobic oxidation protocol of amines