708801
Iron(III) trifluoromethanesulfonate
90%
동의어(들):
Fe(CF3SO3)3, Ferric triflate, Ferric trifluoromethanesulfonate, Fe(CF3SO3)3, Fe(OTf)3, Iron 1,1,1-trifluoromethanesulfonic acid, Iron(III) triflate
로그인조직 및 계약 가격 보기
모든 사진(3)
About This Item
실험식(Hill 표기법):
C3F9FeO9S3
CAS Number:
Molecular Weight:
503.05
MDL number:
UNSPSC 코드:
12161600
PubChem Substance ID:
NACRES:
NA.22
추천 제품
분석
90%
형태
powder
반응 적합성
core: iron
reagent type: catalyst
환경친화적 대안 제품 특성
Catalysis
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mp
183 °C
환경친화적 대안 카테고리
, Aligned
SMILES string
[Fe+3].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F
InChI
1S/3CHF3O3S.Fe/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3
InChI key
OSHOQERNFGVVRH-UHFFFAOYSA-K
일반 설명
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
>230.0 °F
Flash Point (°C)
> 110 °C
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Hai-Jie Song et al.
ChemSusChem, 8(24), 4250-4255 (2015-11-28)
Using a metal triflate and Pd/C as catalysts, alkanes were prepared from bioderived furans in a one-pot hydrodeoxygenation (HDO) process. During the reaction, the metal triflate plays a crucial role in the ring-opening HDO of furan compounds. The entire reaction
Imtiyaz Ahmad Wani et al.
Organic & biomolecular chemistry, 16(16), 2910-2922 (2018-04-06)
Direct and expedient access to densely substituted tetrahydrocarbazoles and tetrahydrocycloheptadiindoles bearing multiple contiguous stereocentres has been achieved via a two-fold divergent diastereoselective (dr up to >99 : 1) transformation of 2-vinylindoles. The high-yielding conversions (yield up to 87%) that are amenable for
Yang Li et al.
Macromolecular bioscience, 20(11), e2000146-e2000146 (2020-06-23)
The conducting polymer polyethylenedioxythiophene doped with polystyrene sulfonate (PEDOT:PSS) has received great attention in the field of wearable bioelectronics due to its tunable high electrical conductivity, air stability, ease of processability, biocompatibility, and recently discovered self-healing ability. It has been
Raffaele Cucciniello et al.
ChemSusChem, 9(23), 3272-3275 (2016-11-24)
The present work deals with the production of monoalkyl glyceryl ethers (MAGEs) through a new reaction pathway based on the reaction of glycidol and alcohols catalyzed by Lewis acid-based catalysts. Glycidol is quantitatively converted with high selectivity (99 %) into MAGEs
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