639860-76-7 Usage
Functional Groups
Amine, Methyl, and Methoxy groups
Structure
A butanamine molecule with a methoxy group at the 2nd carbon and two methyl groups attached to the nitrogen atom
Chemical Class
Amine derivative
Applications
a. Synthesis of pharmaceuticals and organic chemicals
b. Research as a reagent and intermediate in organic synthesis
c. Potential use in the development of new drugs and therapeutic compounds
Basicity
Due to the presence of the amine group, it exhibits basic properties
Solubility
Likely soluble in polar solvents like water and alcohols due to the presence of the amine and methoxy groups
Reactivity
Can undergo reactions typical of amines, such as alkylation, acylation, and nucleophilic substitution
Safety
As with many chemicals, proper handling and safety precautions should be taken when working with 1-Butanamine, 2-methoxy-N,N-dimethyl-(9CI) to avoid potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 639860-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,9,8,6 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 639860-76:
(8*6)+(7*3)+(6*9)+(5*8)+(4*6)+(3*0)+(2*7)+(1*6)=207
207 % 10 = 7
So 639860-76-7 is a valid CAS Registry Number.
639860-76-7Relevant academic research and scientific papers
Hemilabile Ligands in Organolithium Chemistry: Substituent Effects on Lithium Ion Chelation
Ramirez, Antonio,Lobkovsky, Emil,Collum, David B.
, p. 15376 - 15387 (2007/10/03)
The lithium diisopropylamide-mediated 1,2-elimination of 1-bromocyclooctene to provide cyclooctyne is investigated using approximately 50 potentially hemilabile polyethers and amino ethers. Rate laws for selected ligands reveal chelated monomer-based pathways. The dependence of the rates on ligand structure shows that anticipated rate accelerations based on the gem-dimethyl effect are nonexistent and that substituents generally retard the reaction. With the aid of semiempirical and DFT computational studies, the factors influencing chelation are discussed. It seems that severe buttressing within chelates of the substitutionally rich ligands precludes a net stabilization of the chelates relative to nonchelated (η 1-solvated) forms. One ligand-MeOCH2CH2NMe 2-appears to promote elimination uniquely by a higher-coordinate monomer-based pathway.
