31969-04-7 Usage
Uses
Used in Pharmaceutical Industry:
2-(Methyl-2-propen-1-ylamino)ethanol is used as an intermediate in the synthesis of various pharmaceutical compounds for its ability to form stable derivatives and enhance the solubility of active ingredients.
Used in Personal Care Products:
2-(Methyl-2-propen-1-ylamino)ethanol is used as a component in personal care products for its chelating and surfactant properties, which help improve the stability and effectiveness of formulations.
Used in Agricultural Chemicals:
2-(Methyl-2-propen-1-ylamino)ethanol is used in the production of agricultural chemicals for its ability to enhance the solubility and stability of active ingredients, improving their performance in crop protection.
Used as a Corrosion Inhibitor:
2-(Methyl-2-propen-1-ylamino)ethanol is used as a corrosion inhibitor in various industrial applications, protecting metal surfaces from corrosion and extending their service life.
Used as a Surfactant:
2-(Methyl-2-propen-1-ylamino)ethanol is used as a surfactant in detergents and emulsifiers, enhancing the solubilization of oily substances and improving the stability of emulsion systems.
Used in Textile Auxiliaries:
2-(Methyl-2-propen-1-ylamino)ethanol is used in the formulation of textile auxiliaries for its ability to improve the wetting and dyeing properties of fabrics, enhancing the performance and quality of textile products.
It is important to handle 2-(Methyl-2-propen-1-ylamino)ethanol 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.
SYNTHESE DES MORPHOLINES. II. ALLYLATION CHIMIOSELECTIVE DES 2-AMINOALCOOLS, PRODUITS DE DEPART POUR LA FORMATION DES MORPHOLINES.
Dobrev, Alexandre,Spasov, Stefan,Lattes, Armand
, p. 1601 - 1619 (2007/10/02)
La reaction d'allylation des 2-aminoalcools est une reaction chimioselective donnant un acces facile et avec des bons rendements aux alcools correspondants exclusivement N-allyles.Leurs structures ont ete prouvees par spectrometrie de masse, IR et 1H RMN.
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.
