69777-52-2 Usage
Uses
Used in Pharmaceutical Industry:
(2-methylpropyl)Carbamic acid is used as an intermediate in the synthesis of various pharmaceuticals for its ability to form carbamate-based compounds, which have therapeutic properties.
Used in Pesticide and Herbicide Industry:
(2-methylpropyl)Carbamic acid is used as a key intermediate in the manufacturing of carbamate-based pesticides and herbicides, contributing to their effectiveness in controlling pests and unwanted plant growth.
Used in Industrial Chemical Production:
(2-methylpropyl)Carbamic acid is utilized in the production of other industrial chemicals, highlighting its versatility and importance in chemical synthesis.
Due to its potential health and environmental impacts, the use and handling of (2-methylpropyl)Carbamic acid should be carefully regulated and monitored to ensure safety and sustainability in its applications.
Check Digit Verification of cas no
The CAS Registry Mumber 69777-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,7 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69777-52:
(7*6)+(6*9)+(5*7)+(4*7)+(3*7)+(2*5)+(1*2)=192
192 % 10 = 2
So 69777-52-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO2/c1-4(2)3-6-5(7)8/h4,6H,3H2,1-2H3,(H,7,8)
69777-52-2Relevant academic research and scientific papers
Perinu, Cristina,Arstad, Bjornar,Bouzga, Aud. M.,Jens, Klaus-J.
, p. 10167 - 10174 (2014)
Factors influencing the reactivity of selected amine absorbents for carbon dioxide (CO2) capture, in terms of the tendency to form amine carbamate, have been studied. Four linear primary alkanolamines at varying chain lengths (MEA, 3A1P, 4A1B, and 5A1P), two primary amines with different substituents in the β-position to the nitrogen (1A2P and ISOB), a secondary alkanolamine (DEA), and a sterically hindered primary amine (AMP) were investigated. The relationship between the 15N NMR data of aqueous amines and their ability to form carbamate, as determined at equilibrium by quantitative 13C NMR experiments, was analyzed, taking into account structural-chemical properties. For all the amines, the 15N chemical shifts fairly reflected the observed reactivity for carbamate formation. In addition to being a useful tool for the investigation of amine reactivity, 15N NMR data clearly provided evidence of the importance of solvent effects for the understanding of chemical dynamics in CO2 capture by aqueous amine absorbents.
