추천 제품
grade
purum
Quality Level
분석
≥95.0% (AT)
형태
solid
반응 적합성
reagent type: oxidant
mp
121-125 °C (lit.)
122-125 °C
작용기
fluoro
iodo
SMILES string
FC(F)(F)C(=O)O[I](OC(=O)C(F)(F)F)c1ccccc1
InChI
1S/C10H5F6IO4/c11-9(12,13)7(18)20-17(6-4-2-1-3-5-6)21-8(19)10(14,15)16/h1-5H
InChI key
PEZNEXFPRSOYPL-UHFFFAOYSA-N
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애플리케이션
Reactant or reagent for:
- Pummerer-like reactions
- Chemoselective deprotection of dimethoxybenzyl ethers
- Mediating oxidative cycloisomerization
- Tosyloxylation of anilides
기타 정보
Reagent for dehydrogenation and oxidation reactions, review; New reagent for the direct conversions of amides to amines (Hofmann-type rearrangement) and key substance for carboxyterminal peptide sequencing; Smooth dethioacetalization to the carbonyls
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
Tetrahedron Letters, 30, 287-287 (1989)
Organic Syntheses, 66, 132-132 (1988)
Synthesis, 709-709 (1984)
Methods (San Diego, Calif.), 164-165, 18-28 (2019-06-20)
The generation of induced pluripotent stem cell models of human disease requires efficient modification of one or both alleles depending on dominant or recessive inheritance of the disease. To faithfully recapitulate many disease variants, the introduction of a single base
Determination of asparagine and glutamine in polypeptides using bis(I,I-trifluoroacetoxy)iodobenzene.
Analytical biochemistry, 113(1), 149-153 (1981-05-01)
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