55723-10-9 Usage
Uses
Used in Pharmaceutical Industry:
(E)-3-Tetrahydropyranyloxy-1-tributylstannyl-1-propene is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with improved efficacy and reduced side effects, contributing to advancements in medical treatments.
Used in Agrochemical Industry:
In the agrochemical sector, (E)-3-Tetrahydropyranyloxy-1-tributylstannyl-1-propene is employed as a synthetic building block for the creation of novel agrochemicals. Its reactivity and structural diversity enable the development of innovative products that can enhance crop protection and yield.
Used in Fine Chemicals Industry:
(E)-3-Tetrahydropyranyloxy-1-tributylstannyl-1-propene is also utilized in the production of fine chemicals, which are high-purity chemicals used in various applications, such as fragrances, dyes, and specialty chemicals. Its versatility in organic synthesis makes it an essential component in the development of these high-value products.
Used in Organic Synthesis:
As a valuable building block in organic synthesis, (E)-3-Tetrahydropyranyloxy-1-tributylstannyl-1-propene is used for the development of new chemical compounds with diverse applications. Its unique reactivity and structural features allow chemists to explore new reaction pathways and create innovative molecules for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 55723-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,2 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55723-10:
(7*5)+(6*5)+(5*7)+(4*2)+(3*3)+(2*1)+(1*0)=119
119 % 10 = 9
So 55723-10-9 is a valid CAS Registry Number.
55723-10-9Relevant academic research and scientific papers
Non-Pd transition metal-catalyzed hydrostannations: Bu3SnF/PMHS as a tin hydride source
Maleczka Jr., Robert E.,Ghosh, Banibrata,Gallagher, William P.,Baker, Aaron J.,Muchnij, Jill A.,Szymanski, Amy L.
, p. 4000 - 4008 (2013/06/27)
Molybdenum, cobalt, nickel, ruthenium, and rhodium catalyzed alkyne hydrostannations using in situ generated Bu3SnH were studied. In most cases, Bu3SnF+polymethylhydrosiloxane (PMHS) performed well as the in situ source of Bu3/
Regioselective hydrostannations catalyzed by molybdenum isonitrile complexes
Braune, Sascha,Kazmaier, Uli
, p. 26 - 29 (2007/10/03)
Hydrostannations using Mo(CO)3(CNtBu)3 give rise to α-stannylated alcohols and ethers in a highly regioselective fashion. The yields and selectivities obtained with this catalyst are significantly higher in comparison to t
