41784-08-1 Usage
Uses
Used in Pharmaceutical Industry:
4'-Aminoacetophenone hydrochloride is used as a chemical intermediate for the synthesis of various drugs and organic compounds. Its reactivity and functional groups make it a valuable building block in the development of new pharmaceuticals.
Used in Chemical Industry:
In the chemical industry, 4'-Aminoacetophenone hydrochloride is used as a reagent in the production of dyes and pigments. Its aromatic amine structure allows for the formation of various colored compounds, contributing to the coloration of different products.
Used in Industrial Processes:
4'-Aminoacetophenone hydrochloride is used as a water-soluble intermediate due to its hydrochloride form, which can be advantageous in certain industrial processes that require increased solubility for better reaction efficiency or easier handling.
Safety and Regulations:
4'-Aminoacetophenone hydrochloride is subject to strict regulations and must be handled and stored according to safety guidelines to minimize potential health and environmental hazards. Proper training and adherence to safety protocols are essential for those working with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 41784-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,8 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41784-08:
(7*4)+(6*1)+(5*7)+(4*8)+(3*4)+(2*0)+(1*8)=121
121 % 10 = 1
So 41784-08-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO.ClH/c1-6(10)7-2-4-8(9)5-3-7;/h2-5H,9H2,1H3;1H
41784-08-1Relevant articles and documents
Selective and Additive-Free Hydrogenation of Nitroarenes Mediated by a DMSO-Tagged Molecular Cobalt Corrole Catalyst
Sch?fberger, Wolfgang,Timelthaler, Daniel,Topf, Christoph
supporting information, p. 2114 - 2120 (2021/07/22)
We report on the first cobalt corrole that effectively mediates the homogeneous hydrogenation of structurally diverse nitroarenes to afford the corresponding amines. The given catalyst is easily assembled prior to use from 4-tert-butylbenzaldehyde and pyrrole followed by metalation of the resulting corrole macrocycle with cobalt(II) acetate. The thus-prepared complex is self-contained in that the hydrogenation protocol is free from the requirement for adding any auxiliary reagent to elicit the catalytic activity of the applied metal complex. Moreover, a containment system is not required for the assembly of the hydrogenation reaction set-up as both the autoclave and the reaction vessels are readily charged under a regular laboratory atmosphere.
