40987-46-0 Usage
Uses
Used in Pharmaceutical Industry:
4-Methyl-2-morpholinemethanol is used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing medications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Methyl-2-morpholinemethanol is utilized as a precursor in the production of agrochemicals, aiding in the creation of more effective and environmentally friendly pesticides and fertilizers.
Used in Specialty Chemicals Production:
4-Methyl-2-morpholinemethanol is employed as a versatile intermediate in the synthesis of specialty chemicals, enhancing the performance and properties of these chemicals for specific applications.
Used in Polymer, Resin, and Plastics Manufacturing:
4-Methyl-2-morpholinemethanol is used as a raw material in the manufacturing of polymers, resins, and plastics, improving their structural integrity and performance characteristics.
Used in Corrosion Inhibition:
4-Methyl-2-morpholinemethanol is used as a corrosion inhibitor in industrial fluids and water treatment products, protecting metals from corrosion and extending the lifespan of equipment and infrastructure.
It is crucial to handle 4-Methyl-2-morpholinemethanol with care, adhering to proper safety precautions to prevent potential harm from ingestion, inhalation, or skin absorption.
Check Digit Verification of cas no
The CAS Registry Mumber 40987-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,8 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40987-46:
(7*4)+(6*0)+(5*9)+(4*8)+(3*7)+(2*4)+(1*6)=140
140 % 10 = 0
So 40987-46-0 is a valid CAS Registry Number.
40987-46-0Relevant academic research and scientific papers
Intramolecular Cyclization Products from Alkanolamines and Epichlorohydrin
Buriks, Rudy S.,Lovett, Eva G.
, p. 5247 - 5254 (2007/10/02)
Tetriary (2-hydroxyethyl)dialkylamines reacted with epichlorohydrin to form mixtures containing equal amounts of 2-(hydroxymethyl)-4,4-dialkylmorpholinium chlorides and perhydro-6-hydroxy-4,4-dialkyl-1,4-oxazepinium chlorides.Secondary (2-hydroxyethyl)alkylamines gave a 9:1 ratio of the corresponding bases in agreement with the prediction of Baldwin's rules.
