99972-57-3 Usage
Uses
Used in Pharmaceutical Industry:
(5-Nitronaphthalen-1-yl)-methanol is used as a key intermediate in the synthesis of various pharmaceuticals. Its ability to form derivatives with different functional groups allows for the development of new drugs with improved therapeutic properties.
Used in Dye Industry:
(5-Nitronaphthalen-1-yl)-methanol is used as a starting material in the production of dyes. Its versatile chemical properties enable the creation of a wide range of dyes with different colors and properties.
Used in Agrochemical Industry:
(5-Nitronaphthalen-1-yl)-methanol is used in the synthesis of agrochemicals, such as pesticides and herbicides. Its potential to form various derivatives allows for the development of new and effective agrochemicals.
It is important to handle (5-Nitronaphthalen-1-yl)-methanol with care, as nitro compounds are known to be potentially hazardous and can pose risks to human health and the environment if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 99972-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,9,7 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99972-57:
(7*9)+(6*9)+(5*9)+(4*7)+(3*2)+(2*5)+(1*7)=213
213 % 10 = 3
So 99972-57-3 is a valid CAS Registry Number.
99972-57-3Relevant academic research and scientific papers
INTRAMOLECULAR ELECTRON TRANSFER AND DEHALOGENATION OF NITROAROMATIC ANION RADICALS.
Bays,Blumer,Baral-Tosh,Behar,Neta
, p. 320 - 324 (2007/10/02)
A series of nitroaromatic compounds, containing Cl, Br or tosyl groups at various positions, were synthesized and studied by pulse radiolysis in aqueous alcohol solutions. One-electron reduction of the compounds produces the anion radicals which then undergo an intramolecular electron transfer and eliminate X** minus (Cl** minus , Br** minus , or TsO** minus ). The rates of X** minus elimination vary over six orders of magnitude and are affected by the C-X bond dissociation energies, the size and nature of the group bridging the X with the pi system, and the relative positions of these groups. Intramolecular electron transfer through space is also demonstrated. Refs.
