220803-77-0 Usage
Description
N-(4,4-Diethoxybutyl)-forMaMide, also known as a gamma-methylaminobuteraldehyde precursor, is a chemical compound with the chemical properties of a yellow oil. It is characterized by its unique molecular structure, which includes a butyl chain with two ethoxy groups and a formaMide group.
Uses
Used in Pharmaceutical Industry:
N-(4,4-Diethoxybutyl)-forMaMide is used as an intermediate in the synthesis of various pharmaceutical compounds, specifically for the preparation of gamma-methylaminobuteraldehyde. N-(4,4-Diethoxybutyl)-forMaMide serves as a crucial building block in the development of drugs targeting neurological and psychiatric disorders.
Used in Chemical Synthesis:
In the field of organic chemistry, N-(4,4-Diethoxybutyl)-forMaMide is utilized as a versatile reagent for the synthesis of a wide range of organic molecules. Its unique structure allows for various chemical reactions, making it a valuable asset in the creation of new compounds with potential applications in various industries.
Used in Research and Development:
N-(4,4-Diethoxybutyl)-forMaMide is also employed in research and development settings, where it is used to study the properties and behavior of similar chemical compounds. This helps scientists and researchers to better understand the underlying mechanisms and potential applications of these compounds in various fields, including medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 220803-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,8,0 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 220803-77:
(8*2)+(7*2)+(6*0)+(5*8)+(4*0)+(3*3)+(2*7)+(1*7)=100
100 % 10 = 0
So 220803-77-0 is a valid CAS Registry Number.
220803-77-0Relevant articles and documents
Determination of methylputrescine oxidase by high performance liquid chromatography
Feth, Friedhelm,Wray, Victor,Wagner, Karl G.
, p. 1653 - 1655 (1985)
N-Methyl-Δ1-pyrrolinium chloride, the product of the title enzyme, was synthesized by methylation of aminobutyraldehyde diethylacetal followed by acidic cleavage. After purification to homogeneity, it was characterized by NMR and UV spectroscopy. The compound had an absorption maximum at 210 nm; previous data indicating a maximum at 267 nm were shown to arise from an impurity. An HPLC method for the assay of N-methylputrescine oxidase from plant material was developed based on the separation of N-methyl-Δ1-pyrrolinium chloride on a cation exchange column and direct detection at 210 nm. The enzyme activity was measured in the protein fraction extracted from plant roots and treated by gel filtration on disposable PD 10 columns. A Km value of 1.9 mM was determined for methylputrescine and the enzyme from tobacco roots. The enzyme activities from N. tabacum and Datura stramonium were compared.
