82044-22-2 Usage
Chemical structure
The compound consists of a benzylsulfanyl group attached to a pentachlorobenzene core.
Type of compound
It is a type of aromatic thiol, which means it contains a sulfur atom bonded to a carbon atom within an aromatic ring.
Chlorine content
The compound contains multiple chlorine atoms (five) attached to the benzene ring.
Research and industrial applications
It is commonly used as a precursor in the synthesis of various organic compounds.
Versatility
The specific properties and potential uses of the compound are dependent on the nature of the benzylsulfanyl group and the pentachlorobenzene core.
Environmental and health hazards
Due to the presence of chlorine atoms, 1-(benzylsulfanyl)-2,3,4,5,6-pentachlorobenzene may pose environmental and health hazards and should be handled with care and precautions.
Precautions
It is important to follow proper safety protocols and guidelines when working with 1-(benzylsulfanyl)-2,3,4,5,6-pentachlorobenzene to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 82044-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,4 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82044-22:
(7*8)+(6*2)+(5*0)+(4*4)+(3*4)+(2*2)+(1*2)=102
102 % 10 = 2
So 82044-22-2 is a valid CAS Registry Number.
82044-22-2Relevant academic research and scientific papers
Co-C bond cleavage in the reactions of alkyl, benzyl and heteroaromaticmethyl cobaloximes with arene sulfenyl chloride: Homolytic and heterolytic pathways
Gupta,Dixit, Vandana,Das, Indira
, p. 49 - 58 (2007/10/03)
The reactions of arene sulfenyl chlorides, ArSCl, (Ar=Ph, C6Cl5, 2,4 (NO2)2C6H3) with organocobaloximes, RCo(dmgH)2Py, (R=alkyl, benzyl and heteroaromaticmethyl) were carried out under thermal and photochemical conditions. A variety of organic and organometallic products are formed depending upon the substrate cobaloxime. For 3-methoxybenzyl and heteroaromaticmethyl cobaloximes the results suggest that they represent a unique class of cobaloximes whereby both the aromatic ring as well as the Co-C bond are highly activated towards attack by the arene sulfenyl chloride. Both homolytic as well as heterolytic pathways are operative.
