27615-98-1 Usage
Description
TRIBUTYLTIN FLUORIDE POLYMER is a chemical compound that serves as a catalyst in various industrial processes, particularly in the production of plastics, resins, and adhesives. It is a polymer of tributyltin fluoride, which is recognized for its high catalytic activity and stability, making it an efficient and reliable catalyst for a wide range of chemical reactions. The polymer is often utilized in polymerization processes to create high-performance polymers with desirable physical and chemical properties. However, due to its toxic effects on the environment and living organisms, especially marine life, TRIBUTYLTIN FLUORIDE POLYMER is considered a hazardous substance that necessitates careful handling and disposal.
Uses
Used in Chemical Industry:
TRIBUTYLTIN FLUORIDE POLYMER is used as a catalyst for various chemical reactions, enhancing the efficiency and speed of these processes.
Used in Plastics Production:
TRIBUTYLTIN FLUORIDE POLYMER is used as a catalyst in the production of plastics, contributing to the creation of materials with specific physical and chemical properties required for different applications.
Used in Resin Production:
TRIBUTYLTIN FLUORIDE POLYMER is used as a catalyst in the synthesis of resins, which are essential components in coatings, adhesives, and composite materials.
Used in Adhesives Production:
TRIBUTYLTIN FLUORIDE POLYMER is used as a catalyst in the production of adhesives, improving the bonding properties and performance of these materials.
Check Digit Verification of cas no
The CAS Registry Mumber 27615-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,1 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27615-98:
(7*2)+(6*7)+(5*6)+(4*1)+(3*5)+(2*9)+(1*8)=131
131 % 10 = 1
So 27615-98-1 is a valid CAS Registry Number.
InChI:InChI=1/3C4H9.FH.Sn/c3*1-3-4-2;;/h3*1,3-4H2,2H3;1H;/q;;;;+1/p-1/rC12H27FSn/c1-4-7-10-14(13,11-8-5-2)12-9-6-3/h4-12H2,1-3H3
27615-98-1Relevant articles and documents
Fluoro-Substituted Methyllithium Chemistry: External Quenching Method Using Flow Microreactors
Colella, Marco,Degennaro, Leonardo,Higuma, Ryosuke,Ishikawa, Susumu,Luisi, Renzo,Nagaki, Aiichiro,Takahashi, Yusuke,Tota, Arianna
supporting information, p. 10924 - 10928 (2020/05/08)
The external quenching method based on flow microreactors allows the generation and use of short-lived fluoro-substituted methyllithium reagents, such as fluoromethyllithium, fluoroiodomethyllithium, and fluoroiodostannylmethyllithium. Highly chemoselective reactions have been developed, opening new opportunities in the synthesis of fluorinated molecules using fluorinated organometallics.
Palladium complex-catalyzed germylation of allylic halides using (germyl)stannanes
Nakano, Taichi,Ono, Kazuyoshi,Senda, Yoshiya,Migita, Toshihiko
, p. 313 - 317 (2007/10/03)
(Triethylgermyl)tributylstannane reacts metal-selectively with allylic halides at room temperature (r.t.) in the presence of tris(dibenzylideneacetone)dipalladium, Pd2(dba)3CHCl3, to provide an alternative route to allylge
Antifungal sordaridin derivatives
-
, (2008/06/13)
A compound of formula STR1 wherein Z is a tetrahydro-pyrano group selected from STR2 having antifungal activity processes for their preparation and their use in medicines.
