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Geigerin, also known as 2-(2-nitrophenyl)-2-(N,N-diethylamino)ethanol, is a synthetic organic compound that has been used as a chemical warfare agent. It is a colorless, oily liquid with a molecular formula of C12H18N2O3. Geigerin is classified as a psychoactive chemical weapon, which means it can cause severe psychological and physiological effects on humans. It is known to disrupt the central nervous system, leading to symptoms such as hallucinations, confusion, and disorientation. Due to its potential for misuse and harmful effects, the production and stockpiling of geigerin are prohibited under the Chemical Weapons Convention.

436-45-3

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436-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 436-45-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 436-45:
(5*4)+(4*3)+(3*6)+(2*4)+(1*5)=63
63 % 10 = 3
So 436-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O4/c1-6-4-11-13(8(3)15(18)19-11)14(17)12-7(2)10(16)5-9(6)12/h6,8-9,11,13-14,17H,4-5H2,1-3H3/t6-,8+,9+,11+,13+,14+/m0/s1

436-45-3Downstream Products

436-45-3Relevant academic research and scientific papers

Synthesis of sesquiterpene-inspired derivatives designed for covalent binding and their inhibition of the NF-κB pathway

Duplan, Vincent,Serba, Christelle,Garcia, Jose,Valot, Gaelle,Barluenga, Sofia,Hoerle, Melanie,Cuendet, Muriel,Winssinger, Nicolas

, p. 370 - 375 (2014/01/06)

A significant portion of bioactive secondary metabolites are endowed with reactive functionalities that can engage in covalent interactions with their target. Sesquiterpene lactones in particular are rich in Michael acceptors that react with cysteines. Several polycyclic scaffolds derived from total synthesis or readily available polycyclic terpenes were used as the starting point in the synthesis of a library aiming to project mildly reactive functionalities (Michael acceptors or chloroacetates) with diverse geometries. Screening of the library for inhibition of the NF-κB pathway revealed several potent inhibitors that are chemically readily accessible.

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