6270-36-6 Usage
Description
2,2'-[methylenebis(thio)]bis-Benzothiazole, also known as MBTS, is a pale yellow powder with a slight odor, commonly used as a rubber additive in the manufacturing of tires and other rubber products. It acts as an accelerator, promoting the vulcanization process and improving the physical properties of the rubber, such as its tensile strength and resistance to heat and aging. MBTS is also used as a plasticizer and a corrosion inhibitor in various industrial applications. It is considered to be relatively stable and non-toxic when handled and used properly.
Uses
Used in Rubber Industry:
2,2'-[methylenebis(thio)]bis-Benzothiazole is used as a rubber additive for promoting the vulcanization process and improving the physical properties of rubber, such as its tensile strength and resistance to heat and aging.
Used in Plasticizer Industry:
2,2'-[methylenebis(thio)]bis-Benzothiazole is used as a plasticizer in various industrial applications.
Used in Corrosion Inhibition Industry:
2,2'-[methylenebis(thio)]bis-Benzothiazole is used as a corrosion inhibitor in various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6270-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6270-36:
(6*6)+(5*2)+(4*7)+(3*0)+(2*3)+(1*6)=86
86 % 10 = 6
So 6270-36-6 is a valid CAS Registry Number.
6270-36-6Relevant articles and documents
Infrared vibrations of carbon-sulphur bonds in bis(benzoxazole-, benzoimidazole-benzothiazole-2-thiol)methane. Assignments by "selenation"
Cristiani, Franco,Devillanova, Francesco A.,Diaz, Angelo,Verani, Gaetano
, p. 137 - 140 (1983)
The i.r. spectra of the title compounds have been compared with those of the corresponding-2-selenol derivatives.The i.r. vibrational assignments of the thioether links have been made on the basis of the selenation.The moiety CH2-(Y-CH2)2 (Y = S, Se) present in all the compounds considered gives typical absorptions in the fingerprint region.
Bromomethyllithium-mediated chemoselective homologation of disulfides to dithioacetals
Pace, Vittorio,Pelosi, Azzurra,Antermite, Daniele,Rosati, Ornelio,Curini, Massimo,Holzer, Wolfgang
supporting information, p. 2639 - 2642 (2016/02/18)
An efficient, chemoselective homologation of disulfides and diselenides to the corresponding dithio- and diselenoacetals has been developed via the addition of bromomethyllithium. Chemoselectivity is fully preserved in the presence of concomitant electrophilic sites decorating the substrates. The synthetic potential of selected dithioacetals has been evaluated in Feringa-Fa?anas-Mastral-type Pd-catalyzed coupling with an organolithium and in the unusual 1,4-addition to a Weinreb amide.