10220-34-5 Usage
General Description
N-isopropylbenzothiazol-2-sulphenamide is a chemical compound with the molecular formula C11H14N2S2. It is used as an accelerator in the production of rubber and rubber products. N-isopropylbenzothiazol-2-sulphenamide is a type of rubber vulcanization accelerator, which means it speeds up the process by which rubber compounds are converted into a stronger, more durable material. N-isopropylbenzothiazol-2-sulphenamide is also known by the trade name "Accelerator NS." In addition to its use in rubber production, this chemical has been found to have potential applications in the medical field, particularly in the treatment of certain types of cancer. However, further research is needed to fully understand its potential in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 10220-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,2 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10220-34:
(7*1)+(6*0)+(5*2)+(4*2)+(3*0)+(2*3)+(1*4)=35
35 % 10 = 5
So 10220-34-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2S2/c1-7(2)12-14-10-11-8-5-3-4-6-9(8)13-10/h3-7,12H,1-2H3
10220-34-5Relevant articles and documents
ON THE REACTION OF BENZOTHIAZOL-2-YL SULPHENAMIDES WITH PHOSPHITES
Brownbridge, P.,Jowett, I. C.
, p. 311 - 318 (2007/10/02)
A study of the synthesis of phosphoramidates from phosphites and benzothiazol-2-yl-sulphenamides, indicates that a quinquecovalent phosphorane is an intermediate.Since the initial step in this reaction does not involve attack of phosphorus on nitrogen, it is unlikely that these sulphenamides will act as electrophilic aminating agents towards non-phosphorus nucleophiles.An efficient new method for preparing benzothiazol-2-yl-sulphenamides is reported.
Process for the preparation of thiazolesulphenamides
-
, (2008/06/13)
Thiazolesulphenamides, useful as rubber vulcanization accelerators, are made by reaction of a 2-mercapto-thiazole or a 2,2'-dithiazolyl disulphide with ammonia or a primary or secondary amine in the presence of oxygen and a copper catalyst of specified kind.
