32683-02-6 Usage
Uses
Used in Pharmaceutical Industry:
ETHYL 2-AMINO-2-CYANOACETATE OXALATE H2O is used as a key intermediate for the synthesis of various drugs and organic compounds, contributing to the development of new pharmaceuticals and enhancing the therapeutic potential of existing medications.
Used in Chemical Industry:
In the chemical industry, ETHYL 2-AMINO-2-CYANOACETATE OXALATE H2O is utilized as a reagent in organic synthesis, facilitating the creation of a wide range of chemical products and compounds.
Used in Agrochemical Industry:
ETHYL 2-AMINO-2-CYANOACETATE OXALATE H2O is employed in the agrochemical sector, where it serves as a building block for the preparation of biologically active compounds that can be used in the development of pesticides, herbicides, and other agrochemical products to improve crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 32683-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,6,8 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 32683-02:
(7*3)+(6*2)+(5*6)+(4*8)+(3*3)+(2*0)+(1*2)=106
106 % 10 = 6
So 32683-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N2O2/c1-2-9-5(8)4(7)3-6/h4H,2,7H2,1H3
32683-02-6Relevant academic research and scientific papers
On the Polarographic Reduction Mechanism of Some Heterocyclic Compounds
Malik, Wahid U.,Jain, Rajeev
, p. 191 - 194 (2007/10/02)
For evaluating the mechanistic steps, position at d.m.e. and assigning inner or outer sphere path of electrode processes of a number of pyrazole derivatives, thiazoles and their precursors experiments were carried out in the absence and presence of surfactants.All the compounds gave diffusion-controlled, irreversible waves over the entire pH range (2.0-11.0) studied.In presence of surfactants also, diffusion-controlled but more irreversible waves were obtained.In absence and presence of surfactant (CTAB) values of Kapp and αapp for all these compounds were calculated and have been taken as a proof of inner sphere or outer sphere path of the electrode reaction.Results have been explained on the basis of formation of phenylazo-functionalised surfactant as an intermediate species.
