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(2-chloro-2-deuterio-vinyl)-benzene, also known as 2-chloro-2-deuterio-1-phenylethylene, is an organic compound with the molecular formula C8DClH7. It is a halogenated derivative of styrene, where one hydrogen atom is replaced by a deuterium atom (an isotope of hydrogen with one neutron) and another hydrogen atom is replaced by a chlorine atom. (2-chloro-2-deuterio-vinyl)-benzene is characterized by its unique molecular structure, which consists of a benzene ring attached to a vinyl group (C=C) with a chlorine atom and a deuterium atom. Due to its specific isotope composition, it may have applications in chemical research, particularly in the study of reaction kinetics and isotope effects. The compound's properties, such as reactivity and stability, can be influenced by the presence of the heavier deuterium atom, making it a valuable tool for understanding the behavior of molecules in various chemical processes.

3947-94-2

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3947-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3947-94-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,4 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3947-94:
(6*3)+(5*9)+(4*4)+(3*7)+(2*9)+(1*4)=122
122 % 10 = 2
So 3947-94-2 is a valid CAS Registry Number.

3947-94-2Downstream Products

3947-94-2Relevant academic research and scientific papers

REACTIVE INTERMEDIATES IN THE PHOTOLYSIS AND THERMOLYSIS OF 3-CHLORO-3-BENZYLDIAZIRINE

Liu, Michael T. H.,Chishti, Najmul H.,Tencer, Michael,Tomioka, Hideo,Izawa, Yasuji

, p. 887 - 892 (2007/10/02)

The photochemical and thermal decomposition of 3-chloro-3-benzyldiazirine have been studied in different reaction conditions.The decomposition gives rise to benzylchlorocarbene which can rearrange to E and Z chlorostyrene and/or react with the environment.In the presence of acetic acid the main product is 1-chloro-2-phenylethyl acetate.Experiments with acetic acid-d4 showed that some of the chlorostyrene is formed from the carbocation; other experiments conducted with tetramethylethylene as a carbene trapping agent show that the carbene is formed even in the presence of acetic acid.

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