131182-91-7 Usage
Thiazole derivative
A chemical compound containing a thiazole ring This indicates that the core structure of the compound is a thiazole ring, which is a five-membered heterocyclic ring with one sulfur and one nitrogen atom.
Nitro group
A functional group consisting of an oxygen and a nitrogen atom (-NO2) The presence of a nitro group in the compound suggests that it may have certain chemical and biological properties, such as being an oxidizing agent or having potential pharmacological activity.
Trifluoromethyl group
A functional group consisting of a carbon atom bonded to three fluorine atoms (-CF3) The presence of a trifluoromethyl group can influence the compound's reactivity, stability, and lipophilicity, which may affect its biological activity and pharmacokinetic properties.
Phenyl ring
A six-membered carbon ring with alternating single and double bonds The phenyl ring is a common structural motif in organic chemistry and can be found in many pharmaceuticals and agrochemicals.
Potential applications in pharmaceuticals and agrochemicals
The compound may have uses in the development of new drugs and pesticides This suggests that 2-((2-nitro-4-(trifluoromethyl)phenyl)thio)benzo[d]thiazole could be a valuable building block or active ingredient in the development of new products in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 131182-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,1,8 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131182-91:
(8*1)+(7*3)+(6*1)+(5*1)+(4*8)+(3*2)+(2*9)+(1*1)=97
97 % 10 = 7
So 131182-91-7 is a valid CAS Registry Number.
131182-91-7Relevant articles and documents
The [Cu]-catalyzed SNAR reactions: Direct amination of electron deficient aryl halides with sodium azide and the synthesis of arylthioethers under Cu(II) - Ascorbate redox system
Goriya, Yogesh,Ramana
experimental part, p. 7642 - 7650 (2010/12/19)
A one pot [Cu]-promoted SNAr reaction of electron-deficient halobenzenes with sodium azide and the reduction of the intermediate aryl azides under the same Cu(II)-ascorbate redox conditions leading to anilines has been documented. Control experiments revealed that both ascorbate and proline play important role in the reaction path way. Further, the use of this catalytic Cu(II)-ascorbate redox system has been explored for the synthesis of arylthioethers.
