31969-04-7 Usage
General Description
2-(Methyl-2-propen-1-ylamino)ethanol, also known as N-methyl-2-aminoethanol or N-methyl-2-hydroxyethylamine, is a chemical compound commonly used in the production of pharmaceuticals, personal care products, and agricultural chemicals. 2-(Methyl-2-propen-1-ylamino)ethanol is a secondary amine with a hydroxyl functional group, making it a versatile building block for synthesizing various organic compounds. It is also known for its use as a corrosion inhibitor, surfactant, and chelating agent. Additionally, 2-(Methyl-2-propen-1-ylamino)ethanol is used in the formulation of detergents, emulsifiers, and textile auxiliaries due to its ability to solubilize oily substances and enhance the stability of emulsion systems. However, it is important to handle this compound with caution, as it can cause skin and eye irritation, and may be harmful if ingested or inhaled in large quantities.
Check Digit Verification of cas no
The CAS Registry Mumber 31969-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,9,6 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31969-04:
(7*3)+(6*1)+(5*9)+(4*6)+(3*9)+(2*0)+(1*4)=127
127 % 10 = 7
So 31969-04-7 is a valid CAS Registry Number.
31969-04-7Relevant articles and documents
Palladium-catalyzed reactions of N-allylbenzotriazoles with amines and sulfonamides: A facile route to functionalized allylamines and N-allylsulfonamides
Katritzky,Yao,Denisko
, p. 8063 - 8065 (2000)
A variety of functionalized N-allylamines and N-allylsulfonamides are synthesized by Pd(II)- catalyzed intermolecular amination of the corresponding N-allylbenzotriazoles.
Synthesis and preliminary pharmacological activity of aminoalkoxy isosteres of glycolate ester anticholinergics
Fries,Andrako,Hudgins
, p. 1250 - 1254 (2007/10/05)
A series of 2-(N-substituted amino)alkoxy-1,1-diphenylethanols was synthesized and evaluated for anticholinergic activity. The compounds differ structurally from the glycolate ester-type anticholinergic compounds by the bioisosteric substitution of a methylene group for the ester carbonyl moiety. The esters which result from this change have increased lipophilicity compared to their ester isosteres. Compounds in the series have significant anticholinergic activity when tested on isolated rat jejunum or for their ability to inhibit perphenazine-induced catatonia in rats. Structure-activity relationships of the compounds are discussed.
