22246-26-0 Usage
Uses
Used in Organic Synthesis:
6-Nitro-1-tetralone is used as a building block in organic synthesis for the creation of various pharmaceuticals and agrochemicals. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-Nitro-1-tetralone is utilized as a key intermediate in the development of new drugs. Its presence in the molecular structure can influence the pharmacological properties of the final product, contributing to the discovery of novel therapeutic agents.
Used in Research and Development:
6-Nitro-1-tetralone is also used in research and development settings to study its potential pharmacological properties. Scientists are interested in its effects on the central nervous system, which could lead to the development of new treatments for neurological disorders.
Used in Pharmaceutical Industry:
6-Nitro-1-tetralone is used as a precursor in the pharmaceutical industry for the synthesis of various drugs. Its versatility in chemical reactions allows for the creation of a wide range of medicinal compounds with different therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 6-Nitro-1-tetralone is employed as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can enhance their effectiveness in controlling pests and weeds in agricultural settings.
Check Digit Verification of cas no
The CAS Registry Mumber 22246-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,4 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22246-26:
(7*2)+(6*2)+(5*2)+(4*4)+(3*6)+(2*2)+(1*6)=80
80 % 10 = 0
So 22246-26-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3/c12-10-3-1-2-7-6-8(11(13)14)4-5-9(7)10/h4-6H,1-3H2
22246-26-0Relevant academic research and scientific papers
One-pot asymmetric synthesis of either diastereomer of tert-butanesulfinyl- protected amines from ketones
Tanuwidjaja, Jessica,Peltier, Hillary M.,Ellman, Jonathan A.
, p. 626 - 629 (2007/10/03)
A one-pot method for the asymmetric synthesis of tert-butanesulfinyl- protected amines is described. Condensation of aryl alkyl and dialkyl ketones with tert-butanesulfinamide followed by in situ reduction with the appropriate reagent provides either dias
