128350-88-9 Usage
General Description
3-HYDROXY-2-OXO-3-TRIFLUOROMETHYL-6-METHYLINDOLINE is a chemical compound with the molecular formula C10H8F3NO2. It is a derivative of 6-methylindoline and contains a trifluoromethyl group and a hydroxyl group on the aromatic ring. 3-HYDROXY-2-OXO-3-TRIFLUOROMETHYL-6-METHYLINDOLINE is commonly used as a building block in organic synthesis and can be used to create various pharmaceutical and agrochemical compounds. It has also been studied for its potential biological activities, including its anti-inflammatory and antioxidant properties. Additionally, it has been used as a versatile intermediate in the production of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 128350-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,5 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 128350-88:
(8*1)+(7*2)+(6*8)+(5*3)+(4*5)+(3*0)+(2*8)+(1*8)=129
129 % 10 = 9
So 128350-88-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H8F3NO2/c1-5-2-3-6-7(4-5)14-8(15)9(6,16)10(11,12)13/h2-4,16H,1H3,(H,14,15)
128350-88-9Relevant articles and documents
Trifluoromethyl-containing N-acylmethylenequinone imines as novel highly electrophilic agents
Dyachenko, Victor I.,Peregudov, Aleksandr S.,Chkanikov, Nikolai D.
, p. 868 - 878 (2008/03/13)
The strategy of searching for highly electrophilic agents in a class of chemically inert compounds - methylenequinone imines - was developed and successfully performed. The first representative of such electrophiles - N-acyl-α-methoxycarbonyl-α-trifluoromethyl-p-methylenequinone imine 6 - was synthesized. Its reactions with N-, O- and C-nucleophiles were investigated that gave various derivatives of α-trifluoromethyl-α-amino(oxy) acids as well as ?,?,?-trifluoropropionic acids. 3-Chloro-3-trifluoro-1,3-dihydroindol-2-ones were first obtained and their reactions with nucleophiles were studied with 1-aza-3-trifluoroindene-2-ones being formed as intermediates.
