3653-11-0 Usage
Uses
Used in Organic Synthesis:
2,3-Butanediamine, N,N,N',N'-tetraethylis used as a catalyst in various organic synthesis processes. Its ability to facilitate reactions and improve yields makes it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Polymer and Resin Production:
In the polymer and resin industry, 2,3-Butanediamine, N,N,N',N'-tetraethylis used as a catalyst to promote the formation of polymer chains and improve the properties of the final product. Its use in this application contributes to the development of high-performance materials with enhanced mechanical, thermal, and chemical resistance.
Used as a Corrosion Inhibitor:
2,3-Butanediamine, N,N,N',N'-tetraethylcan be used as a corrosion inhibitor in various industrial applications. Its ability to form protective films on metal surfaces helps prevent corrosion and extends the service life of equipment and structures.
Used in Fuel Additives:
As a component in fuel additives, 2,3-Butanediamine, N,N,N',N'-tetraethylcan improve the performance and efficiency of fuels. Its use in this application can lead to reduced emissions, improved combustion, and enhanced fuel stability.
Check Digit Verification of cas no
The CAS Registry Mumber 3653-11-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3653-11:
(6*3)+(5*6)+(4*5)+(3*3)+(2*1)+(1*1)=80
80 % 10 = 0
So 3653-11-0 is a valid CAS Registry Number.
3653-11-0Relevant articles and documents
Investigations on photochemistry of o-allyloxy-/crotyloxyacetophenones: Formation of unexpected intramolecular arene-olefin addition products on n-π* excitation of ketones
Singh, Rajinder,Ishar
, p. 7595 - 7606 (2002)
Photochemistry of o-allyloxy-/crotyloxyacetophenones (6a,b) has been investigated under different conditions. Irradiation of 6a,b in dry benzene, under N2 atmosphere (Pyrex filter), led to the isolation of (syn)-2-ethenyl/propenyl-3-hydroxy-3-m
Photolysis of Tertiary Amines in the Presence of CO2: The Paths to Formic Acid, α-Amino Acids, and 1,2-Diamines
Berton, Mateo,Mello, Rossella,Acerete, Rafael,González Núnez, María Elena
, p. 96 - 103 (2018/02/19)
The photolysis of triethylamine (1a) in the presence of carbon dioxide leads to the hydrogenation of CO2, the α-C-C coupling of 1a, and the CO2 insertion into the α-C-H σ-bond of amine 1a. This reaction is proposed to proceed through the radical ion pair [R3N?+·CO2?-] generated by the photoionization of amine 1a and the electron capture by CO2. The presence of lithium tetrafluoroborate in the reaction medium promotes the efficient and stereoselective α-C-C coupling of 1a by enhancing the production of α-dialkylamino radicals and the isomerization of N,N,N′,N′-tetraethylbutane-2,3-diamine (4a).
