100330-70-9 Usage
Deuterated derivative
2 deuterium atoms This compound contains two deuterium atoms, which are heavy isotopes of hydrogen, making it a deuterated version of the non-deuterated 1-phenyl-1-(dimethylamino)ethylene.
Application in organic chemistry
Stable isotope-labeled compound The presence of deuterium atoms makes this compound useful in organic chemistry as a stable isotope-labeled compound for research and analytical purposes.
Study of reaction mechanisms
Valuable tool The deuterium labeling allows researchers to track the compound's behavior and better understand the mechanisms behind various chemical reactions.
Investigation of metabolic pathways
Tracer compound 2,2-dideutero-1-phenyl-1-(dimethylamino)ethylene can be used as a tracer to study how the compound is metabolized and processed within biological systems.
Synthesis and breakdown of organic molecules
Tracing studies The compound can be used to investigate the synthesis and breakdown of other organic molecules, providing insights into their chemical properties and behavior.
Drug development and therapeutic treatments
Potential applications The compound may be utilized in the development of new drugs and therapeutic treatments, as its deuterium labeling can help researchers understand how these substances interact with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 100330-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,3 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100330-70:
(8*1)+(7*0)+(6*0)+(5*3)+(4*3)+(3*0)+(2*7)+(1*0)=49
49 % 10 = 9
So 100330-70-9 is a valid CAS Registry Number.
100330-70-9Relevant articles and documents
New rearrangement in the reaction of 1-aryl-1-(dimethylamino)-ethylenes with nitrosobenzenes. Molecular and crystal structure of N1,N1-dimethyl-N2-phenyl-2-oxo(3-pyridyl)acetamidine
Koikov, L. N.,Terent'ev, P. B.,Yufit, D. S.,Struchkov, Yu. T.,Zubarev, V. E.
, p. 1664 - 1674 (2007/10/02)
The reaction of aryleneamines Ar(NMe2)C=CH2 (Ar= Ph, 2-Py, 3-Py, 4-Py) with nitrosobenzenes p-RC6H4NO (R= H, Cl, Br, Me, MeO) in benzene or ether (20 deg C) is accompanied by rearrangement and leads to N1,N1-dimethyl-N2-aryl-2-oxo(aryl)-acetamidines (20-40percent) and a mixture of products from reduction of the nitroso compounds.The effect of temperature on the yield of the amidines is insignificant, and the presence of one or two methyl groups at the β position of the enamine leads to the formation of only azoxybenzene.Accepting substituents in the nitrosobenzenes do not affect the yield of the rearrangement products, while donors reduce it.The reaction is accompanied by the formation of radical particles, and a reaction scheme is proposed.The acid hydrolysis of the obtained amidines and their reduction with lithium aluminum hydride were investigated.
