所有图片(3)
About This Item
经验公式（希尔记法）:
C14H14F3NO4S
CAS号:
分子量:
349.33
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
检测方案
96%
形式
solid
mp
85-91 °C
储存温度
2-8°C
SMILES字符串
[O-]S(=O)(=O)C(F)(F)F.C[n+]1ccccc1OCc2ccccc2
InChI
1S/C13H14NO.CHF3O3S/c1-14-10-6-5-9-13(14)15-11-12-7-3-2-4-8-12;2-1(3,4)8(5,6)7/h2-10H,11H2,1H3;(H,5,6,7)/q+1;/p-1
InChI key
DUXHYQYOPHEFGC-UHFFFAOYSA-M
应用
法律信息
经FSURF许可销售，美国专利7,754,909及相关专利适用。标签许可证（不受规模限制）在购买时授予最终用户。
警示用语：
Danger
危险分类
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Dudley, G. B. et al.
Synlett, 3142-3142 (2005)
Jumreang Tummatorn et al.
The Journal of organic chemistry, 72(23), 8962-8964 (2007-10-16)
Triethylamine (Et3N) mediates esterification reactions between the title reagent (1) and carboxylic acids. Alcohols, phenols, amides, and other sensitive functionality are not affected; a dual role for Et3N as a promoter and a scavenger is postulated. Benzyl esters are obtained
Kevin W C Poon et al.
The Journal of organic chemistry, 71(10), 3923-3927 (2006-05-06)
2-Benzyloxy-1-methylpyridinium triflate (1) is a stable, neutral organic salt that converts alcohols into benzyl ethers upon warming. The synthesis and reactivity of 1 are described herein. Benzylation of a wide range of alcohols occurs in good to excellent yield.
商品
Dudley Reagents provide mild protection for alcohols and carboxylic acids in synthesis.
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