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(4-isopropyl-3-p-tolyl-3H-thiazol-2-ylidene)-p-tolyl-amine is a complex organic compound characterized by its unique molecular structure. It features a thiazole ring system, which is a five-membered heterocyclic ring containing sulfur and nitrogen. The compound is further adorned with two p-tolyl groups, which are toluene (a methyl group attached to a benzene ring) moieties. One of these p-tolyl groups is connected to the thiazole ring, while the other is linked to an amine group, which consists of a nitrogen atom bonded to two hydrogen atoms and a p-tolyl group. The presence of an isopropyl group, a three-carbon alkyl chain with a branching structure, adds to the complexity of the molecule. (4-isopropyl-3-p-tolyl-3H-thiazol-2-ylidene)-p-tolyl-amine is likely to have specific chemical properties and reactivity due to its structure, and it may be of interest in various chemical or pharmaceutical applications.

82686-70-2

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82686-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82686-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,8 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82686-70:
(7*8)+(6*2)+(5*6)+(4*8)+(3*6)+(2*7)+(1*0)=162
162 % 10 = 2
So 82686-70-2 is a valid CAS Registry Number.

82686-70-2Relevant academic research and scientific papers

Synthesis and Mercuration of Some New 3-Aryl-2-arylimino-4,5-disubstituted-δ4-thiazolines and Their Fungicidal and Bactericidal Activities

Mohanty, J.,Mahapatra, G. N.

, p. 52 - 55 (2007/10/02)

A series of new 3-aryl-2-arylimino-4,5-disubstituted-Δ4-thiazolines (I) have been synthesised by condensing various ketones having active methylene group with sym-diarylthioureas in the presence of bromine.The thiazolines (I) on mercuration with one equivalent of mercuric acetate in acetic acid give 3-(acetoxymercuriaryl)-2-arylimino-4,5-disubstituted-Δ4-thiazolines (II).All the compounds have been assayed against the fungus Pyricularia oryzae (Cav) and the bacteria Esch. coli and Staph. aureus, and the structure-activity relationship has been discussed.

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