17390-72-6 Usage
Uses
Used in Pharmaceutical Industry:
Tributylstannanylium butane-1-thiolate is used as a catalyst for the synthesis of organic compounds in the pharmaceutical industry. Its ability to accelerate difficult reactions and produce high yields of desired products makes it a valuable tool in the development of new drugs and pharmaceutical agents.
Used in Agrochemical Industry:
In the agrochemical industry, tributylstannanylium butane-1-thiolate is utilized as a catalyst in the production of organic compounds used in the formulation of pesticides, herbicides, and other agrochemical products. Its catalytic properties help improve the efficiency and effectiveness of these compounds.
Used in Materials Industry:
Tributylstannanylium butane-1-thiolate is employed as a catalyst in the synthesis of organic compounds for the materials industry. Its ability to facilitate the formation of new carbon-carbon or carbon-heteroatom bonds contributes to the development of advanced materials with specific properties for various applications, such as polymers, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 17390-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,9 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17390-72:
(7*1)+(6*7)+(5*3)+(4*9)+(3*0)+(2*7)+(1*2)=116
116 % 10 = 6
So 17390-72-6 is a valid CAS Registry Number.
17390-72-6Relevant academic research and scientific papers
DIRECT SYNTHESIS OF PROTECTED THIOLS BY TRIBUTYLSTANNYL GROUP
Ueno, Yoshio,Nozomi, Mamoru,Okawara, Makoto
, p. 1199 - 1202 (2007/10/02)
Organic thiocyanates react with tributyltin hydride under homolytic conditions to give thiostannanes (Bu3Sn-SR), which are air-stable and high boiling protected forms of the parent thiols.
Functionally substituted organotin compounds I. Addition of thiols to alkenyltin compounds
Ayrey,Brasington,Poller
, p. 105 - 109 (2008/10/08)
3-(Trialkylstannyl)propyl aryl sulphides (R3SnCH2CH2CH2SR′; R = Me, Et, Bu; R′ = Ph, p-tolyl) were prepared by the addition of arenethiols to allyltrialkyltin compounds. Preferential cleavage of the allyl group
