14302-46-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Production:
3-AMINO-1-PROPANOL HYDROCHLORIDE is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its presence in these compounds contributes to their biological activity and effectiveness.
Used in Chiral Ligand and Catalyst Synthesis:
3-AMINO-1-PROPANOL HYDROCHLORIDE is utilized as a precursor in the production of chiral ligands and catalysts. Its unique structure allows for the creation of enantioselective catalysts, which are crucial in asymmetric synthesis for producing specific enantiomers of chiral compounds.
Used in Biochemical and Molecular Biology Applications:
3-AMINO-1-PROPANOL HYDROCHLORIDE is used as a buffer solution in biochemical and molecular biology research. Its ability to maintain a stable pH environment is essential for various laboratory procedures and experiments.
Used in Dye and Pigment Manufacturing:
3-AMINO-1-PROPANOL HYDROCHLORIDE is employed as an intermediate in the manufacturing of dyes and pigments. Its chemical properties contribute to the color development and stability of these products.
Used in Surfactant, Lubricant, and Corrosion Inhibitor Production:
3-AMINO-1-PROPANOL HYDROCHLORIDE is used in the production of surfactants, lubricants, and corrosion inhibitors due to its amphiphilic nature. This characteristic allows it to reduce surface tension in liquids, improve the flow properties of lubricants, and protect metal surfaces from corrosion.
Check Digit Verification of cas no
The CAS Registry Mumber 14302-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,0 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14302-46:
(7*1)+(6*4)+(5*3)+(4*0)+(3*2)+(2*4)+(1*6)=66
66 % 10 = 6
So 14302-46-6 is a valid CAS Registry Number.
14302-46-6Relevant academic research and scientific papers
Geneste, Herve,Hesse, Manfred
, p. 15199 - 15214 (1998)
Five 13C-dilabeled constitution isomers of 4-coumaroylspermidines were prepared in nine to eleven steps: N1,4-di[(E)-4-coumaroyl]-(5,8- 13C2)spermidine (13b), N1-[(E)-4-coumaroyl]-(5,8-13C2)spermidine (17b), N1,8-di[(E)-4-coumaroyl]-(1,4-13C2)spermidine (20b), N4-[(E)-4- coumaroyl]-(1,4-13C2)spermidine (24b) and N1,4,8-tri[(E)-4-coumaroyl]- (5,8-13C2)spermidine (26). The two 13C-atoms were subsequently introduced using labeled potassium cyanide. The synthesis proceeds through stepwise construction of the polyamine backbone including protection and deprotection steps of the amino functions. Based on 1H-1H NOE interactions, the preliminary study of their binding reveals that 20b binds to tRNA in the same way as spermidine does, whereas 24b and 26 do not show any NOE effects with the tRNA protons.
