96784-58-6 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-(3-methyl-4-nitrophenyl)is employed as a key intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows for a wide range of chemical reactions, making it a valuable building block in the development of new molecules with desired properties.
Used in Research Laboratories:
As a reagent, Ethanone, 1-(3-methyl-4-nitrophenyl)is widely used in research laboratories for conducting experiments and studying chemical reactions. Its distinct properties, such as its yellow color and reactivity, make it an ideal candidate for investigating various chemical processes and mechanisms.
Used as a Dye:
Due to its inherent yellow color, Ethanone, 1-(3-methyl-4-nitrophenyl)is utilized as a dye in various applications, including textiles, plastics, and other materials. Its colorfastness and stability make it a preferred choice for imparting yellow shades to different products.
Used in Pharmaceutical Industry:
Ethanone, 1-(3-methyl-4-nitrophenyl)has been studied for its potential pharmaceutical properties, particularly in the field of drug discovery. Its unique structure and reactivity make it a promising candidate for the development of new drugs with therapeutic applications. Researchers are exploring its potential as a precursor for the synthesis of bioactive compounds and its use in the design of novel pharmaceutical agents.
Check Digit Verification of cas no
The CAS Registry Mumber 96784-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,8 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96784-58:
(7*9)+(6*6)+(5*7)+(4*8)+(3*4)+(2*5)+(1*8)=196
196 % 10 = 6
So 96784-58-6 is a valid CAS Registry Number.
96784-58-6Relevant articles and documents
Reactions of 1-(benzotriazol-1-yl)-1-phenoxyalkane and (benzotriazol-1- yl)ethoxyphenylmethane anions with nitroarenes: A new approach to alkyl and aryl p-nitroaryl ketones
Katritzky, Alan R.,Chassaing, Christophe,Toader, Dorin,Gill, Katherine
, p. 504 - 505 (2007/10/03)
p-Nitroaryl alkyl ketones and p-nitroaryl aryl ketones are prepared regioselectively by reactions of non-functionalized nitroarenes and benzotriazole stabilized carbanions.
Conjugate addition of Grignard reagents to para-substituted nitrobenzenes
Bentley, Stephen J.,Milner, David J.
, p. 1 - 3 (2007/10/02)
Nitrobenzenes bearing masked aldehyde, ketone and ketoester functions at the 4-position undergo conjugate addition with Grignard reagents in THF at -15 deg C.Sequential treatment of the 4-substituted nitrobenzenes with primary or secondary alkyl magnesium
GRIGNARD REAGENTS SELECTIVE ATTACK TO NITROARENIC FUNCTION IN THE PRESENCE OF OTHER ELECTROPHILIC GROUPS
Bartoli, G.,Bosco, M.,Dalpozzo, R.
, p. 115 - 118 (2007/10/02)
Exclusive alkylation of the nitroarenic system takes place in competitive reactions of RMgX with nitrobenzene and various electrophiles such as ketones, esters, cyanoand iodo-derivatives and in reactions with some functionalized nitrobenzenes, only aldehy
