추천 제품
Quality Level
분석
97%
반응 적합성
reaction type: click chemistry
refractive index
n20/D 1.36 (lit.)
bp
153 °C (lit.)
density
1.723 g/mL at 25 °C (lit.)
작용기
carboxylic acid
fluoro
SMILES string
OC(=O)C(F)(F)S(F)(=O)=O
InChI
1S/C2HF3O4S/c3-2(4,1(6)7)10(5,8)9/h(H,6,7)
InChI key
VYDQUABHDFWIIX-UHFFFAOYSA-N
일반 설명
2,2-Difluoro-2-(fluorosulfonyl)acetic acid reagent is employed as a difluorocarbene source for difluoromethylation of phenolic hydroxyl groups.
애플리케이션
2,2-Difluoro-2-(fluorosulfonyl)acetic acid may be used in the following processes:
- Preparation of 1-difluoromethyl-2-oxo-1,2-dihydropyridine analogs by reacting with the corresponding 2-chloropyridines.
- Prepration of silyl fluorosulfonyldifluoroacetate as new highly efficient difluorocarbene reagent for cyclopropanation of alkenes.
- Regio- and stereoselective free radical fluoroalkylation of terminal alkenes and alkynes with iododifluoromethanesulfonamides.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 2 Oral - Skin Corr. 1A
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
230.0 °F - closed cup
Flash Point (°C)
110 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
이미 열람한 고객
Free radical fluoroalkylation of terminal alkenes and alkynes with iododifluoromethanesulfonamides.
Science China: Chemistry, 54(1), 95-102 (2011)
Free radical fluoroalkylation of terminal alkenes and alkynes with iododifluoromethanesulfonamides
Science China: Chemistry, 54, 95-102 (2011)
Trimethylsilyl fluorosulfonyldifluoroacetate (TFDA): a new, highly efficient difluorocarbene reagent
Journal of Fluorine Chemistry, 125, 459-469 (2004)
Preparation and use of a new difluorocarbene reagent
Organic Syntheses, 80, 172-176 (2003)
Organic letters, 8(17), 3805-3808 (2006-08-11)
[reaction: see text] A novel one-pot synthesis of N-difluoromethyl-2-pyridones is described. N-(Pyridin-2-yl)acetamide derivatives were excellent precursors for the preparation of N-difluoromethyl-2-pyridone derivatives. Difluoromethylation of 2-acetaminopyridine derivatives was achieved with sodium chlorodifluoroacetate as a difluorocarbene source in the presence of a
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.