6056-50-4 Usage
Uses
Used in Organic Synthesis:
TRICYCLOHEXYLTIN HYDRIDE is used as a reducing agent in organic synthesis for its ability to facilitate chemical reactions, contributing to the formation of desired products in the synthesis process.
Used in Rubber and Plastics Production:
In the industry of rubber and plastics, TRICYCLOHEXYLTIN HYDRIDE is employed in the production process, likely due to its reducing properties that can influence the polymerization or cross-linking reactions necessary for creating these materials.
Given the compound's hazardous nature, it is imperative to handle TRICYCLOHEXYLTIN HYDRIDE with care, using proper protective equipment to minimize the risk of respiratory, skin, and eye irritation, as well as other potential health hazards associated with exposure to this toxic substance.
Check Digit Verification of cas no
The CAS Registry Mumber 6056-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6056-50:
(6*6)+(5*0)+(4*5)+(3*6)+(2*5)+(1*0)=84
84 % 10 = 4
So 6056-50-4 is a valid CAS Registry Number.
InChI:InChI=1/C38H31ClN4O7/c1-49-30-18-22(19-31(50-2)33(30)44)32-27-16-17-40-36(47)42(25-13-7-4-8-14-25)37(48)43(40)29(27)21-28-34(45)41(26-15-9-12-24(39)20-26)35(46)38(28,32)23-10-5-3-6-11-23/h3-16,18-20,28-29,32,44H,17,21H2,1-2H3
6056-50-4Relevant academic research and scientific papers
HETEROGENEOUS ORGANOTIN CATALYSTS
-
Page/Page column 5, (2010/06/22)
Supported heterogeneous organotin catalysts of the formula X1, X2, or X3: wherein Z is a spacer group; Y is an insoluble phenyl-group containing copolymer; R1, R2, R3, R5, and R6 are independently selected from halogen, alkyl, alkylene, phenyl, vinyl, allyl, naphthyl, aralkyl, and Z; and R4 is alkyl, alkylene, phenyl, vinyl, allyl, naphthyl, or aralkyl.
General routes to functional organotin trichlorides and trialkoxides involving the tricyclohexylstannyl group
Jousseaume, Bernard,Lahcini, Mohammed,Rascle, Marie-Claude,Ribot, Fran?ois,Sanchez, Clément
, p. 685 - 689 (2008/10/08)
New functional organotin trialkoxides have been prepared in two steps from the corresponding organotricyclohexyltins, which were obtained by coupling an organometal species with tricyclohexyltin chloride, by reaction of (tricyclohexylstannyl)lithium with
