82244-58-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in the compound, which is 7 carbon (C), 5 hydrogen (H), 1 deuterium (^2H), 1 bromine (Br), and 1 sulfur (S) atoms.
Explanation
1-bromo-4-^2H3-methylthiobenzene is derived from thiobenzene, a compound consisting of a benzene ring with a sulfur atom replacing one of the hydrogen atoms.
Explanation
The bromine atom is one of the substituents attached to the benzene ring, which contributes to the compound's chemical properties and reactivity.
Explanation
The compound is used as a reactant in organic synthesis, particularly for the preparation of other substituted thiobenzenes. It is also utilized in labeling studies and the production of radiolabeled compounds for medical and research purposes.
Explanation
The deuterium-labeled methyl group in 1-bromo-4-^2H3-methylthiobenzene makes it useful for studying chemical reactions and metabolic pathways involving methyl groups, as the deuterium atom can be easily detected and distinguished from regular hydrogen atoms.
Explanation
Due to its unique structure and properties, 1-bromo-4-^2H3-methylthiobenzene has various applications in both organic chemistry and biomedical research, including the synthesis of new compounds and the study of biological processes.
Derivative of thiobenzene
Yes
Bromine atom
Attached to the benzene ring
Deuterium-labeled methyl group
^2H3
Applications
Organic synthesis, labeling studies, and radiolabeled compounds production
Usefulness in chemical reactions and metabolic pathways
Yes
Applications in organic chemistry and biomedical research
Yes
Check Digit Verification of cas no
The CAS Registry Mumber 82244-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,4 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82244-58:
(7*8)+(6*2)+(5*2)+(4*4)+(3*4)+(2*5)+(1*8)=124
124 % 10 = 4
So 82244-58-4 is a valid CAS Registry Number.
82244-58-4Relevant articles and documents
Visible-light-promoted cross-coupling reactions of aryldiazonium salts with S-methyl-D3 sulfonothioate or Se-methyl-D3 selenium sulfonate: Synthesis of trideuteromethylated sulfides, sulfoxides, and selenides
Wang, Shun-Yi,Huang, Cheng-Mi,Li, Jian,Ai, Jing-Jing,Liu, Xin-Yu,Rao, Weidong
supporting information, p. 9128 - 9132 (2020/12/02)
A novel visible-light-photocatalytic deuterated thiomethylation/methylselenation of aryldiazonium salts utilizing S/ Se-methyl-d3 sulfonothioate has been developed. The mild conditions and the various functional groups provide a green protocol for the efficient and rapid introduction of the S-CD3 or Se-CD3 group with useful levels of deuterium content (>91% D). Trideuteromethyl sulfoxides have also been successfully chemoselectively observed by simple atmospheric changes under photocatalytic conditions.
