535936-86-8 Usage
Uses
Used in Pharmaceutical Industry:
Methyl-2-amino-2-cyclopropyla cetate hydrochloride is used as an intermediate in the synthesis of pharmaceuticals for its sedative, anxiolytic, and muscle relaxant properties. It is particularly valuable in the development of treatments for anxiety and related disorders due to its potential therapeutic effects.
Used in Agrochemical Industry:
Methyl-2-amino-2-cyclopropyla cetate hydrochloride is also used as an intermediate in the synthesis of agrochemicals, contributing to the development of various agricultural products and solutions.
Used in Drug Synthesis:
As a building block in the synthesis of pharmaceutical compounds, methyl-2-amino-2-cyclopropyla cetate hydrochloride plays a crucial role in the creation of new and innovative medications, enhancing the therapeutic options available for various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 535936-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,5,9,3 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 535936-86:
(8*5)+(7*3)+(6*5)+(5*9)+(4*3)+(3*6)+(2*8)+(1*6)=188
188 % 10 = 8
So 535936-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2/c1-9-6(8)5(7)4-2-3-4/h4-5H,2-3,7H2,1H3
535936-86-8Relevant academic research and scientific papers
Photochemical Deracemization at sp3-Hybridized Carbon Centers via a Reversible Hydrogen Atom Transfer
Bach, Thorsten,Breitenlechner, Stefan,Gro?kopf, Johannes,Plaza, Manuel,Seitz, Antonia,Storch, Golo
supporting information, p. 21241 - 21245 (2021/12/27)
A photochemical deracemization of 5-substituted 3-phenylimidazolidine-2,4-diones (hydantoins) is reported (27 examples, 69%-quant., 80–99% ee). The reaction is catalyzed by a chiral diarylketone which displays a two-point hydrogen bonding site. Mechanistic evidence (DFT calculations, radical clock experiments, H/D labeling) suggests the reaction to occur by selective hydrogen atom transfer (HAT). Upon hydrogen binding, one substrate enantiomer displays the hydrogen atom at the stereogenic center to the photoexcited catalyst allowing for a HAT from the substrate and eventually for its conversion into the product enantiomer. The product enantiomer is not processed by the catalyst and is thus enriched in the photostationary state.
Substituted aryl 1,4-pyrazine derivatives
-
, (2008/06/13)
Substituted aryl 1,4-pyrazine derivatives and their use in treating anxiety disorders, depression and stress related disorders are disclosed.
