所有图片(2)
About This Item
线性分子式:
(C6H5S)3CH
CAS号:
分子量:
340.53
Beilstein:
1914230
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
98%
表单
solid
mp
39-41 °C (lit.)
官能团
thioether
SMILES字符串
S(C(Sc1ccccc1)Sc2ccccc2)c3ccccc3
InChI
1S/C19H16S3/c1-4-10-16(11-5-1)20-19(21-17-12-6-2-7-13-17)22-18-14-8-3-9-15-18/h1-15,19H
InChI key
YOQHDHPBEXTHCP-UHFFFAOYSA-N
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应用
Tris(phenylthio)methane has been used in the preparation of:
- 1-phenylthio-tetrahydroisoquinolines via activated Pictet-Spengler cyclization
- homoallylchalcogenoacetals via reaction with allylsilanes in the presence of a Lewis acid
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
Thioorthoesters in the activated Pictet-Spengler cyclization. Synthesis of 1-thiosubstituted tetrahydroisoquinolines and carbon? carbon bond formation via sulfonyl iminium ions generated from N,S-sulfonyl acetals.
Silveira CC, et al.
Tetrahedron Letters, 44(32), 6137-6140 (2003)
Lewis acid-catalyzed coupling reactions of allylsilanes with tris (phenylchalcogeno) methane. Synthesis of homoallylchalcogenoacetals.
Silveira CC, et al.
Tetrahedron Letters, 37(34), 6085-6088 (1996)
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