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1-Benzotriazol-2-yl-3-(toluene-4-sulfonyloxy)-propane, also known as BTSP, is a chemical compound with the molecular formula C17H16N2O4S2. It is a white crystalline solid that is soluble in organic solvents such as acetone, ethyl acetate, and dichloromethane. BTSP is primarily used as a coupling agent in the rubber industry, particularly in the production of tires, hoses, and other rubber products. It enhances the adhesion between rubber and various substrates, such as steel, fabric, and other materials, by forming covalent bonds between the rubber and the substrate. This results in improved mechanical properties, such as tensile strength and abrasion resistance, of the final product. Additionally, BTSP has been studied for its potential applications in other fields, such as pharmaceuticals and materials science, due to its unique chemical structure and reactivity.

2690-91-7

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2690-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2690-91-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,9 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2690-91:
(6*2)+(5*6)+(4*9)+(3*0)+(2*9)+(1*1)=97
97 % 10 = 7
So 2690-91-7 is a valid CAS Registry Number.

2690-91-7Downstream Products

2690-91-7Relevant academic research and scientific papers

Synthesis and pharmacological evaluation of aryl/heteroaryl piperazinyl alkyl benzotriazoles as ligands for some serotonin and dopamine receptor subtypes

Boido, Alessandro,Canu Boido, Caterina,Sparatore, Fabio

, p. 263 - 275 (2001)

Thirteen [(aryl/heteroaryl-piperazinyl)alkyl]benzotriazoles were prepared as potential trazodone- and buspirone-like drugs. The synthesized compounds displayed from moderate to good affinity to the serotonin 5-HT1A receptor and only modest or poor affinity to the dopamine D2 receptor, similar to buspirone. The introduction of substituents on the benzotriazole ring did not improve the affinity to the 5-HT1A receptor, compared to the previously described unsubstituted derivatives. In a general pharmacological screening, which concerned only three of these compounds so far (5, 7 and 13), several in vitro and in vivo activities were observed.The guinea pig ileum contractions, induced either electrically or by several agonists, were strongly inhibited; at higher concentrations also the spontaneous tone of the guinea pig trachea was reduced. Compound 13 exhibited good analgesic activity in mice in the formalin-induced algesia and in the writhing test. The same at 30 mgkg-1 p.o. also displayed antihypertensive activity probably related to calcium channel blockade and adrenergic α1 antagonism. In binding assays, 13 showed a IC50=580 nM for displacing [3H]prazosin from α1 receptor.Finally, compound 5 (and, to a minor extent, compound 13) protected mice against potassium cyanide induced hypoxia. Copyright

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