T83801
三苯基氯甲烷
97%
别名:
三苯基甲基氯, 氯三苯甲烷, 氯代三苯甲烷
登录 查看组织和合同定价。
选择尺寸
变更视图
关于此项目
线性分子式:
(C6H5)3CCl
化学文摘社编号:
分子量:
278.78
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-986-4
Beilstein/REAXYS Number:
397363
MDL number:
Assay:
97%
assay
97%
bp
230-235 °C/20 mmHg (lit.)
mp
109-112 °C (lit.)
SMILES string
ClC(c1ccccc1)(c2ccccc2)c3ccccc3
InChI
1S/C19H15Cl/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
InChI key
JBWKIWSBJXDJDT-UHFFFAOYSA-N
Application
三苯甲基氯可用作以下应有的催化剂：
- Ritter型合成，通过萘酚，芳基醛和乙腈进行一锅三组分反应，合成1-氨基烷基-2-萘酚。
- 通过偶苯酰与醛、伯胺以及乙酸铵进行一锅多组分反应，合成1,2,4,5-四取代咪唑。
- 在无溶剂条件下通过酚、芳香醛和酰胺进行一锅多组分反应制备酰胺烷基酚。
- 通过芳香醛、胺和β-酮酯进行一锅多组分反应合成取代哌啶。
胺、醇和硫醇的保护剂。
Still not finding the right product?
Explore all of our products under 三苯基氯甲烷
signalword
Danger
hcodes
Hazard Classifications
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
Trityl chloride as an efficient organic catalyst for one-pot, five-component and diastereoselective synthesis of highly substituted piperidines
Sajadikhah SS, et al.
Research on Chemical Intermediates, 40(2), 723-736 (2014)
Trityl chloride as an efficient organic catalyst for the synthesis of 1-amidoalkyl-2-naphtols in neutral media at room temperature
Khazaei A, et al.
Applied Catalysis A: General, 386(1-2), 179-187 (2010)
One pot synthesis of 1, 2, 4, 5-tetrasubstituted-imidazoles catalyzed by trityl chloride in neutral media
Moosavi-Zare AR, et al.
Royal Society of Chemistry Advances, 4(105), 60636-60639 (2014)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| T83801-100G | 04061837379161 |
| T83801-500G | 04061837379185 |
| T83801-25G | 04061837379178 |