16906-37-9 Usage
Description
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE, also known as BTE, is a dithiole-containing chemical compound with two benzylthio groups on a cis-1,2-ethylene backbone. It is widely used in organic synthesis and coordination chemistry due to its ability to form stable complexes with transition metals. BTE's versatility and value in research and industry make it a promising candidate for various applications, including catalysis, chelating, materials science, and as a building block in the synthesis of organic molecules.
Uses
Used in Organic Synthesis:
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE is used as a building block for the synthesis of organic molecules, leveraging its unique structure and reactivity to create a variety of compounds with diverse properties and applications.
Used in Coordination Chemistry:
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE is used as a ligand for the formation of stable complexes with transition metals. Its ability to chelate metals enhances the stability and reactivity of these complexes, making BTE a valuable component in coordination chemistry.
Used in Catalytic Reactions:
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE is used as a catalyst or a catalyst precursor in various chemical reactions. Its metal complexes can facilitate and enhance the rates of reactions, improving the efficiency and selectivity of synthetic processes.
Used in Materials Science:
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE is used in the development of new materials with unique properties. Its ability to form stable complexes and its structural features make it a promising candidate for applications in materials science, such as the creation of novel polymers, sensors, or electronic devices.
Used in Research and Development:
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE is used as a versatile chemical in various fields of research and development. Its potential applications in catalysis, chelating, materials science, and organic synthesis make it an invaluable tool for scientists and researchers working on innovative projects and discoveries.
Check Digit Verification of cas no
The CAS Registry Mumber 16906-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,0 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16906-37:
(7*1)+(6*6)+(5*9)+(4*0)+(3*6)+(2*3)+(1*7)=119
119 % 10 = 9
So 16906-37-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H16S2/c1-3-7-15(8-4-1)13-17-11-12-18-14-16-9-5-2-6-10-16/h1-12H,13-14H2/b12-11-
16906-37-9Relevant articles and documents
The role of palladium catalyst and base in stereoselective transformations of (E)-2-chlorovinylsulfides
Rubina, Kira,Abele, Edgars,Arsenyan, Pavel,Fleisher, Mendel,Popelis, Juris,Gaukhman, Alexander,Lukevics, Edmunds
, p. 7603 - 7607 (2003)
Stereoselective transformations of 2-chlorovinylsulfides in the presence of soluble (t-BuOK) or insoluble (solid KOH or Cs2CO 3/18-crown-6) base and palladium catalyst (dppb)Pd(OAc)2 have been studied. Depending on the sub
Vinylidenchlorid als Synthesereagenz fuer Schwefelheterocyclen
Schroth, Werner,Moegel, Liena
, p. 30 - 31 (2007/10/02)
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