396715-58-5 Usage
Uses
Used in Chemical Synthesis Industry:
DABCO is utilized as a catalyst in the formation of polyurethane polymers, which are essential in the production of flexible and rigid foams, coatings, adhesives, and elastomers. Its catalytic properties facilitate the reaction process, leading to the creation of high-quality polymers with desirable properties.
Used in Pharmaceutical and Agrochemical Synthesis:
In the pharmaceutical and agrochemical industries, DABCO serves as a catalyst in the synthesis of various compounds. Its ability to accelerate reaction rates and improve yields makes it a valuable tool in the development of new drugs and agrochemicals, contributing to advancements in healthcare and agriculture.
Used in High-Performance Material Production:
DABCO is employed as a catalyst in the production of high-performance materials, such as advanced composites and specialty polymers. Its catalytic properties enable the synthesis of materials with unique properties, including high strength, durability, and resistance to extreme conditions, making them suitable for applications in aerospace, automotive, and electronics industries.
It is crucial to handle and store DABCO with care due to its potential health and environmental risks. Proper management and safety measures should be implemented to minimize any adverse effects associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 396715-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,6,7,1 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 396715-58:
(8*3)+(7*9)+(6*6)+(5*7)+(4*1)+(3*5)+(2*5)+(1*8)=195
195 % 10 = 5
So 396715-58-5 is a valid CAS Registry Number.
396715-58-5Relevant articles and documents
Exploiting long-lived molecular fluorescence
Nau, Werner M.,Huang, Fang,Wang, Xiaojuan,Bakirci, Huseyin,Gramlich, Gabriela,Marquez, Cesar
, p. 161 - 167 (2007/10/03)
Fluorophores based on the azo chromophore 2,3-diazabicyclo[2.2.2]oct-2-ene, referred to as fluorazophores, display an exceedingly long fluorescence lifetime. Besides the use in time-resolved screening assays, where the long-lived fluorescence can be time-gated, thereby reproving the signal to background ratio, a distinct application of fluorazophores lies in the area of biopolymer dynamics. For this purpose, one chain end is labeled with a fluorazophore and the other one with an efficient fluorescence quencher. The fluorescence lifetime of the probe/quencher-labeled peptide then reflects the kinetics of intramolecular end-to-end collision. Applications to polypeptides are described and control experiments which establish the nature of the quenching mechanism as a diffusive process requiring intimate probe/quencher contact are described.
A fluorescence-based method for direct measurement of submicrosecond intramolecular contact formation in biopolymers: An exploratory study with polypeptides
Hudgins, Robert R.,Huang, Fang,Gramlich, Gabriela,Nau, Werner M.
, p. 556 - 564 (2007/10/03)
A fluorescent amino acid derivative (Fmoc-DBO) has been synthesized, which contains 2,3 diazabicyclo[2.2.2]oct-2-ene (DBO) as a small, hydrophilic fluorophore with an extremely long fluorescence lifetime (325 ns in H2O and 505 ns in D2/su
