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Methyl (phenyl-3-d)sulfane, also known as methyl-3-deuteriophenylsulfane, is a chemical compound with the molecular formula C7H7DS. It is a deuterated analog of methyl phenyl sulfane, where one hydrogen atom in the phenyl group is replaced by a deuterium atom. methyl (phenyl-3-d)sulfane is primarily used as a reagent in organic synthesis, particularly in the preparation of various sulfur-containing compounds and as a tracer in chemical reactions to study reaction mechanisms and kinetics. Methyl (phenyl-3-d)sulfane is a colorless liquid with a characteristic sulfurous odor and is sensitive to air and moisture, requiring storage under an inert atmosphere. Its deuterium labeling makes it a valuable tool for researchers to probe the behavior of sulfur-containing molecules in various chemical transformations.

823-79-0

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823-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 823-79-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 823-79:
(5*8)+(4*2)+(3*3)+(2*7)+(1*9)=80
80 % 10 = 0
So 823-79-0 is a valid CAS Registry Number.

823-79-0Upstream product

823-79-0Downstream Products

823-79-0Relevant academic research and scientific papers

Hydrogen-Bond-Donor Solvents Enable Catalyst-Free (Radio)-Halogenation and Deuteration of Organoborons

Yang, Yi,Gao, Xinyan,Zeng, Xiaojun,Han, Junbin,Xu, Bo

, p. 1297 - 1300 (2021)

A hydrogen bond donor solvent assisted (radio)halogenation and deuteration of organoborons has been developed. The reactions exhibited high functional group tolerance and needed only an ambient atmosphere. Most importantly, compared to literature methods, our conditions are more consistent with the principals of green chemistry (e.g., metal-free, strong oxidant-free, more straightforward conditions).

Ion-neutral complex formation and hydrogen-shifts in the alkene loss from ionized alkyl phenyl thioethers in the gas phase

Van Amsterdam,Ingemann,Nibbering

, p. 43 - 51 (2007/10/02)

The mechanistic aspects of alkene loss from ionized ethyl- and n-propyl phenyl thioethers have been studied by use of deuterium labelling and tandem mass spectrometry. Loss of ethene from the molecule ion of ethyl phenyl thioether proceeds predominantly b

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