추천 제품
양식
liquid
Quality Level
구성
2 M CrO3 in aqueous H2SO4
반응 적합성
core: chromium
reagent type: catalyst
reagent type: oxidant
density
1.298 g/mL at 25 °C
SMILES string
O=[Cr](=O)=O.OS(O)(=O)=O
InChI
1S/Cr.H2O4S.3O/c;1-5(2,3)4;;;/h;(H2,1,2,3,4);;;
InChI key
HNPXHFOTGAXAJY-UHFFFAOYSA-N
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일반 설명
- Jones reagent is a solution of chromium trioxide in aqueous sulfuric acid.
- Using acetone as a reaction solvent, the reagent is usually used for the oxidation of primary and secondary alcohols to carboxylic acids and ketones, respectively.
- The oxidation is very rapid and exothermic.
- The reagent tolerates a variety of functionalities, such as, for example, unsaturated bonds, which are rarely oxidized.
For a comprehensive review of chromium-based reagents, see "Oxidation of Alcohols to Aldehydes and Ketones" by Tojo and Fernández, Springer Berlin, 2006, 1-97.
애플리케이션
Jones reagent can be used:
- In the oxidative cleavage of various alkenes into carboxylic acids and ketones using a catalytic amount of osmium tetroxide.
- To prepare symmetrical binaphthols by oxidative dehydrodimerization of substituted naphthols.
- To synthesize acyl-naphthols and substituted isocoumarins from 2-(4-hydroxy-but-1-ynyl)benzaldehydes.
신호어
Danger
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1A - Eye Dam. 1 - Met. Corr. 1 - Muta. 1B - Ox. Liq. 1 - Repr. 2 - Resp. Sens. 1 - Skin Corr. 1A - Skin Sens. 1 - STOT RE 1 Inhalation - STOT SE 3
표적 기관
Respiratory system
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
이미 열람한 고객
Jones, E. R. H.
Journal of the Chemical Society, 3019-3019 (1953)
Jones, E. R. H.
Journal of the Chemical Society, 457-457 (1953)
Tunable Synthesis of 3-Acyl-2-naphthols and 3-Substituted Isocoumarins via Jones Reagent Promoted Cascade Reactions of 2-(4-Hydroxy-but-1-ynyl) benzaldehydes
He Y, et al.
The Journal of Organic Chemistry, 78(20), 10178-10191 (2013)
Jones, E. R. H.
Journal of the Chemical Society, 2548-2548 (1953)
Bladon, P.; et al.
Journal of the Chemical Society, 2402-2402 (1951)
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