80222-96-4 Usage
Uses
Used in Pharmaceutical Industry:
2-Aminopropanamide hydrochloride is used as a reagent in the synthesis of pharmaceuticals for its ability to react with a wide range of organic compounds, contributing to the development of new drugs and the production of existing ones.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Aminopropanamide hydrochloride is utilized as a reagent in the synthesis of agrochemicals, aiding in the production of compounds that are essential for crop protection and enhancement of agricultural yields.
Used in Fine Chemicals Industry:
2-Aminopropanamide hydrochloride is employed in the preparation of various fine chemicals, which are high-purity, specialty chemicals used in a range of applications, including the fragrance, flavor, and cosmetic industries.
Used in Biochemical Research and Development:
2-Aminopropanamide hydrochloride is also used in the research and development of new biochemical compounds, playing a crucial role in advancing scientific understanding and the creation of innovative products in the field of biochemistry.
Used in Medicine and Drug Discovery:
Due to its reactivity with a broad spectrum of organic compounds, 2-Aminopropanamide hydrochloride may have potential applications in the field of medicine and drug discovery, where it can be instrumental in the synthesis of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 80222-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,2 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80222-96:
(7*8)+(6*0)+(5*2)+(4*2)+(3*2)+(2*9)+(1*6)=104
104 % 10 = 4
So 80222-96-4 is a valid CAS Registry Number.
80222-96-4Relevant academic research and scientific papers
Kato, Yasuo,Asano, Yasuhisa,Nakazawa, Akiko,Kondo, Kiyosi
, p. 5743 - 5754 (1989)
The first stereoselective synthesis of D-amino acid N-alkyl amides was achieved by the use of D-aminopeptidase from Ochrobactrum anthropi.The enzyme immobilized by urethane prepolymer PU-6 catalyzed aminolysis reaction of racemic amino acid esters in organic solvents.
Synthesis of α-amino dithioesters and endothiodipeptides
Hartke, Klaus,Barrmeyer, Stephan
, p. 251 - 256 (2007/10/03)
The α-amino ester hydrochlorides (1) are converted into N-protected α-amino amides (3), α-amino thioamides (4) and α-amino dithiomethylesters (5). Condensation of 5 with the alkali salts of α-amino acids gives rise to the endothiodipeptide alkali salts (7). Johann Ambrosius Barth 1996.
