175390
三苯基碳五氯锡酸
别名:
Trityl pentachlorostannate
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关于此项目
线性分子式:
(C6H5)3CSnCl5
化学文摘社编号:
分子量:
539.30
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
EC Number:
239-426-9
MDL number:
InChI key
LJHTYNWDYRJYIH-UHFFFAOYSA-I
InChI
1S/C19H15.5ClH.Sn/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;;;;/h1-15H;5*1H;/q+1;;;;;;+4/p-5
SMILES string
Cl[Sn-](Cl)(Cl)(Cl)Cl.c1ccc(cc1)[C+](c2ccccc2)c3ccccc3
functional group
phenyl
Quality Level
Application
Triphenylcarbenium pentachlorostannate can be used:
- In the study of cationic polymerization reactions of 3,6-dibromo-9-(2,3-epoxypropyl)carbazole using the microcalorimetric technique.
- In the synthesis of diarylcyclohexanones, the key intermediates for the preparation of antiprotozoals.
- As an initiator in the photopolymerization of carbazolyl derived epoxy monomers.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Diarylcyclohexanones: synthons for new bicyclic compounds
Ahmad S, et al.
Monatshefte fur Chemie / Chemical Monthly, 143(1), 145-152 (2012)
Polymerization of 3, 6-dibromo-9-(2, 3-epoxypropyl) carbazole with triphenylcarbenium salts
Gravzulevivcius JV, et al.
European Polymer Journal, 28(5), 539-545 (1992)
Cationic ring-opening polymerization of carbazolyl-containing epoxy monomers by triphenyl carbenium salts as thermal-and photolatent initiators
Lazauskaite R, et al.
Monatshefte fur Chemie / Chemical Monthly, 140(5), 565-565 (2009)
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