7404-78-6 Usage
Uses
Used in Pharmaceutical and Agricultural Chemical Synthesis:
3-nitro-1-phenylbutan-1-one is used as a precursor for the synthesis of various pharmaceuticals and agricultural chemicals. Its unique chemical structure allows it to be easily modified and incorporated into more complex molecules, making it a valuable building block in the development of new drugs and agrochemicals.
Used in Perfume and Flavoring Production:
3-nitro-1-phenylbutan-1-one is used as a key ingredient in the production of perfumes and flavorings due to its distinct odor. Its unique scent profile can be utilized to create a wide range of fragrances and flavors, enhancing the sensory experience of various products.
Used in Organic Synthesis:
3-nitro-1-phenylbutan-1-one is employed as a building block in organic synthesis, allowing chemists to create more complex molecules with diverse applications. Its versatile chemical properties make it a valuable component in the synthesis of various organic compounds.
Used in Dye and Pigment Manufacturing:
3-nitro-1-phenylbutan-1-one is utilized as an intermediate in the manufacturing of dyes and pigments. Its unique chemical structure contributes to the color and stability of these products, making it an essential component in the production of high-quality dyes and pigments.
Used in the Preparation of Specialized Chemicals:
3-nitro-1-phenylbutan-1-one is employed in the preparation of other specialized chemicals, such as intermediates for the synthesis of various industrial and consumer products. Its versatility and unique properties make it a valuable component in the development of new and innovative chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 7404-78-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7404-78:
(6*7)+(5*4)+(4*0)+(3*4)+(2*7)+(1*8)=96
96 % 10 = 6
So 7404-78-6 is a valid CAS Registry Number.
7404-78-6Relevant academic research and scientific papers
Radical and Ionic Reactions of (Benzoylmethyl)mercurials
Russell, Glen A.,Kulkarni, Shekhar V.,Khanna, Rajive K.
, p. 1080 - 1086 (2007/10/02)
Photolysis of PhCOCH2HgCl or (PhCOCH2)2Hg yields benzoylmethyl radicals which can be trapped by anions such as Me2C=NO2-, RC(CO2Et)2-, RC(O-)=CH2 or by other electron-rich systems such as (RO)3P, N-methylpyrrole, enamines, or norbornene.Electron transfer from the adduct radicals to the mercurials yields PhCOCH2A from the anions A-, PhCOCH2P(O)(OR)2 from P(OR)3, and the phenacyl derivative from N-methylpyrrole or enamines.Easily oxidized anions such as PhCOCPh2- or PhC(CH3)=NO2- react with PhCOCH2* by electron transfer to yield the dimer derived from the anion.Addition of PhCOCH2* to norbornene yields a substituted 3-benzoylpropyl radical which cyclizes at the ortho position of the benzoyl group to give the α-tetralone derivative.
Regioselective Generation and Diastereoselective Reactions in the β-Position of Nitro Groups of Secondary Nitroalkanes through α,β-Doubly Deprotonated Derivatives (Super-enamines)
Braendli, Urs,Eyer, Martin,Seebach, Dieter
, p. 575 - 588 (2007/10/02)
Open-chain (2-nitropropane, -butane, -pentane, -hexane) and cyclic (nitrocyclopentane, -hexane) secondary nitroalkanes (1) were doubly deprotonated with one equivalent each of n- and t-butyllithium in THF/HMPT or DMPU.Bis(lithiooxy)enamines (2, dianion de
