28636-16-0 Usage
Uses
Used in Organic Synthesis:
(E)-3-Aminoacrylaldehyde is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions and contribute to the formation of complex molecular structures.
Used in Pharmaceutical Production:
(E)-3-Aminoacrylaldehyde is used as an intermediate in the production of various pharmaceuticals, highlighting its importance in the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
(E)-3-Aminoacrylaldehyde is also utilized as an intermediate in the production of agrochemicals, indicating its role in the agricultural industry for the development of pesticides and other related products.
Used in Amino Acid and Peptide Synthesis:
(E)-3-Aminoacrylaldehyde is used as a key building block in the synthesis of certain amino acids and peptides, which are essential components of proteins and vital for various biological functions.
Used in Material Development:
(E)-3-Aminoacrylaldehyde has been studied for its potential use in the development of new materials, suggesting its applicability in the field of material science and engineering.
Used in Therapeutic Applications for Neurological Diseases:
(E)-3-Aminoacrylaldehyde is being investigated for its possible therapeutic applications in the treatment of neurological disorders, showcasing its potential in the medical and pharmaceutical sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 28636-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,6,3 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28636-16:
(7*2)+(6*8)+(5*6)+(4*3)+(3*6)+(2*1)+(1*6)=130
130 % 10 = 0
So 28636-16-0 is a valid CAS Registry Number.
28636-16-0Relevant academic research and scientific papers
1H and 13C NMR spectra and isomerism of 3-aminoacroleins
Gomez-Sanchez, Antonio,Paredes-Leon, Rocio,Campora, Juan
, p. 154 - 162 (2007/10/03)
A set of 3-alkylaminoacroleins (R1NHCH=CHCH=O, R1 = alkyl) were studied by 13C and 1H NMR spectroscopy in solutions of different solvents and, for the simplest representative of the series, 3-methylaminoacrolein, at different temperatures. The equilibrium solutions of these compounds consists of mixtures of the chelated ZZE form (Z geometry around the =C - C=O single bond and the C=C bond, and E geometry around the C - N bond) and the two E configurational isomers having the E disposition around the =C - C=O single bond and differing in the disposition around the C - N bond (EEZ and EEE forms). The relative proportions of the three isomers depend on solvent polarity, concentration, bulk of substituent R1 and temperature. The EEZ isomer is the most abundant in polar solvents, while the concentration of the ZZE form increases in non-polar solvents and when increasing the bulk of R1. A lineshape 1H NMR study for 3-methylaminoacrolein in CDCl3 gave a ΔG? value of 66.0 kJ mol-1 at 303 K for the EEZ → EEE conversion. The presence of other tautomeric forms was not observed.
