80866-94-0 Usage
Uses
Used in Pharmaceutical Industry:
3,5-Dinitro-2-methylbenzyl alcohol is used as a precursor for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Pesticide Industry:
In the pesticide industry, 3,5-dinitro-2-methylbenzyl alcohol is utilized as a starting material for the production of effective pest control agents, enhancing agricultural productivity and crop protection.
Used in Dye Production:
3,5-Dinitro-2-methylbenzyl alcohol is used as an intermediate in the manufacturing process of dyes, playing a crucial role in the creation of colorants for various applications.
Used in Explosives Industry:
This chemical compound is also employed as a component in the production of explosives, highlighting its importance in the development of pyrotechnic and demolition materials.
Used in Medicine and Healthcare:
3,5-Dinitro-2-methylbenzyl alcohol is used as a potent antimicrobial agent in the medical and healthcare fields, helping to combat infections and promote public health.
Used in Nanotechnology Research:
3,5-DINITRO-2-METHYLBENZYL ALCOHOL has been studied for its potential applications in nanotechnology, where it may contribute to the advancement of nanoscale devices and materials with unique properties.
Used in Organic Synthesis:
3,5-Dinitro-2-methylbenzyl alcohol is used as a precursor in the synthesis of new organic compounds, expanding the scope of chemical research and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 80866-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,6 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80866-94:
(7*8)+(6*0)+(5*8)+(4*6)+(3*6)+(2*9)+(1*4)=160
160 % 10 = 0
So 80866-94-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O5/c1-5-6(4-11)2-7(9(12)13)3-8(5)10(14)15/h2-3,11H,4H2,1H3
80866-94-0Relevant academic research and scientific papers
Li, Xiangmin,Wang, Sinan,Li, Tengfei,Li, Jian,Li, Hao,Wang, Wei
, p. 5634 - 5637 (2013)
An organocatalytic highly enantioselective Michael-aldol cascade access to valuable chiral dihydronaphthalenes has been realized. Notably, the strategy via activation of nucleophilic alkyl chains by introducing nitro, chloro, or CF3 group(s) at the ortho- and/or para-position(s) on an aromatic ring renders them readily deprotonated to produce highly reactive nulecophilic species in the cascade process under mild conditions.
