36719-40-1 Usage
Description
(1E)-1-phenyl-3,3-di(propan-2-yl)triaz-1-ene is a chemical compound with the molecular formula C16H22N2. It is a derivative of triazole, a five-membered heterocyclic ring containing three nitrogen atoms. (1E)-1-phenyl-3,3-di(propan-2-yl)triaz-1-ene features a phenyl group attached to one end of the triazole ring, as well as two isopropyl groups attached to the other nitrogen atom. The (1E) designation indicates that the compound contains a carbon-carbon double bond in a specific stereochemical configuration. This chemical may have various potential applications, including in organic synthesis, pharmaceutical research, and as a building block for more complex chemical structures. Its specific properties and potential uses would depend on further study and testing.
Uses
Used in Organic Synthesis:
(1E)-1-phenyl-3,3-di(propan-2-yl)triaz-1-ene is used as a building block for the synthesis of more complex organic compounds. Its unique structure and functional groups make it a versatile component in the creation of various organic molecules.
Used in Pharmaceutical Research:
(1E)-1-phenyl-3,3-di(propan-2-yl)triaz-1-ene is used as a starting material or intermediate in the development of new pharmaceuticals. Its triazole core and substituents may contribute to the compound's biological activity, making it a candidate for further exploration in drug discovery.
Used in Chemical Research:
(1E)-1-phenyl-3,3-di(propan-2-yl)triaz-1-ene is used as a research tool to study the properties and reactivity of triazole-containing compounds. Its synthesis and reactions can provide insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge.
Check Digit Verification of cas no
The CAS Registry Mumber 36719-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,1 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36719-40:
(7*3)+(6*6)+(5*7)+(4*1)+(3*9)+(2*4)+(1*0)=131
131 % 10 = 1
So 36719-40-1 is a valid CAS Registry Number.
36719-40-1Relevant articles and documents
Synthesis of Aryl Trimethylstannane via BF3·OEt2-Mediated Cross-Coupling of Hexaalkyl Distannane Reagent with Aryl Triazene at Room Temperature
Mao, Shuai,Chen, Zhengkai,Wang, Lu,Khadka, Daulat Bikram,Xin, Minhang,Li, Pengfei,Zhang, San-Qi
, p. 463 - 471 (2019/01/10)
BF3·OEt2-mediated cross-coupling of (SnMe3)2 with aryl triazene offers a new strategy for the synthesis of aryl stannane. A variety of synthetically useful aryl trimethylstannanes were produced in moderate to good yields with this metal-free approach. One-pot sequential Stille cross-coupling with different aryl bromides provides a short entry to both symmetrical and unsymmetrical biaryl compounds.
Synthesis of triazenes with nitrous oxide
Kiefer, Gregor,Riedel, Tina,Dyson, Paul J.,Scopelliti, Rosario,Severin, Kay
, p. 302 - 305 (2015/02/18)
Triazenes are valuable compounds in organic chemistry and numerous applications have been reported. Furthermore, triazenes have been investigated extensively as potential antitumor drugs. Here, we describe a new method for the synthesis of triazenes. The procedure involves a reagent which is rarely used in synthetic organic chemistry: nitrous oxide (N2O, laughing gas ). Nitrous oxide mediates the coupling of lithium amides and organomagnesium compounds while serving as a nitrogen donor. Despite the very inert character of nitrous oxide, the reactions can be performed in solution under mild conditions. A key advantage of the new procedure is the ability to access triazenes with alkynyl and alkenyl substituents. These compounds are difficult to prepare by conventional methods because the required starting materials are unstable. Some of the new alkynyltriazenes were found to display high cytotoxicity in in vitro tests on ovarian and breast cancer cell lines.
