16499-88-0 Usage
Description
3-Butoxypropanamine is a clear colorless liquid that serves as a key intermediate in the synthesis of various organic compounds, particularly N-functionalized bis(phosphino)amine ligands with ether, thioether, and pyridyl tethers.
Uses
Used in Chemical Synthesis Industry:
3-Butoxypropanamine is used as a precursor in the synthesis of N-functionalized bis(phosphino)amine ligands for [application reason]. These ligands are essential in the development of catalysts and coordination complexes, which find applications in various chemical transformations and homogeneous catalysis processes.
Used in Pharmaceutical Industry:
3-Butoxypropanamine is used as a building block in the synthesis of pharmaceutical compounds for [application reason]. Its ability to form stable complexes with metal ions makes it a valuable component in the development of drug candidates with potential therapeutic applications.
Used in Material Science:
3-Butoxypropanamine is used as a component in the development of advanced materials for [application reason]. Its compatibility with various functional groups allows for the creation of novel materials with unique properties, such as improved stability, reactivity, or selectivity in chemical processes.
Flammability and Explosibility
Notclassified
Check Digit Verification of cas no
The CAS Registry Mumber 16499-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,9 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16499-88:
(7*1)+(6*6)+(5*4)+(4*9)+(3*9)+(2*8)+(1*8)=150
150 % 10 = 0
So 16499-88-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H17NO/c1-2-3-6-9-7-4-5-8/h2-8H2,1H3/p+1
16499-88-0Relevant articles and documents
Aldose epimerization by Ni(II): effect of ether-containig alkylenediamine ligands
Osanai, Shuichi,Inaba, Kiyoshi,Yoshikawa, Sadao
, p. 289 - 295 (2007/10/02)
Several N-substituted ethylenediamine (en) Ni(II) derivatives containing ether linkages were prepared in order to study the effect of ligand structure on C-2 epimerization of aldohexoses.The reagent consisted of a Ni(II)-alkyenediamine derivative in methanol.The presence of ether linkages in the ligand increased the solubilty of the complexes, and resulted in an increase in the rate of epimerization.Epimerization occured rapidly under mild conditions, and the same equilibrium point was reached regardless of whether the reaction was started from glucose or mannose.Among the ligands studied, N,N'-dialkylethylenediamine was the most effective in C-2 epimerization.