1608-69-1 Usage
Uses
Used in Pharmaceutical Industry:
[formyl(methyl)amino]methyl acetate is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique chemical structure allows it to be a valuable building block in the development of new medications, contributing to the advancement of healthcare.
Used in Pesticide Industry:
In the pesticide industry, [formyl(methyl)amino]methyl acetate is utilized as a key component in the production of different types of pesticides. Its role in this industry is crucial for the development of effective and environmentally friendly pest control solutions.
Used in Organic Synthesis:
[formyl(methyl)amino]methyl acetate is used as a reactant in organic synthesis, where it plays a vital role in the preparation of other chemical compounds. Its versatility and reactivity make it a valuable asset in the field of organic chemistry, enabling the creation of a wide range of products.
Used in Chemical Manufacturing:
This organic compound is also employed in the chemical manufacturing industry, where it serves as an intermediate for the production of various organic compounds. Its presence in this industry highlights its importance in the synthesis of a diverse array of chemicals, further emphasizing its utility and applicability across different sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 1608-69-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1608-69:
(6*1)+(5*6)+(4*0)+(3*8)+(2*6)+(1*9)=81
81 % 10 = 1
So 1608-69-1 is a valid CAS Registry Number.
1608-69-1Relevant academic research and scientific papers
Direct vs. Indirect Mechanisms in Organic Electrochemistry. Estimates of Activation Energies for Hydrogen Atom Transfer Processes of Relevance in Indirect Mechanisms Using the Bond Energy-Bond Order (BEBO) and Equibonding Methods
Eberson, Lennart
, p. 481 - 492 (2007/10/02)
Activation energies for a number of hydrogen abstraction reactions of interest in mechanistic organic electrochemistry have been calculated using the bond energy-bond-order (BEBO) and equibonding method.The main emphasis has been put on processes with bearing on the problem of deciding between direct and indirect mechanisms in anodic oxidation, viz. acyloxylation, hydroxylation, methoxylation, nitrooxylation, cyanation, carbomethoxylation and azidation.The results indicate that indirect mechanisms might play a more important role than presently assumed.
