ChemicalBook Optimization Suppliers |
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主な危険性 | Xi | Rフレーズ | 36/37/38-36/38 | Sフレーズ | 26-36-37/39 | WGK Germany | 3 | RTECS 番号 | BZ2605000 | F | 9-23 | 自然発火温度 | 225 °C | TSCA | Yes | 国連危険物分類 | IRRITANT | HSコード | 29124900 | 毒性 | sce-hmn:lyms 1 mmol/L MUREAV 206,17,88 |
| m-アニスアルデヒド Usage And Synthesis |
外観 | 無色~黄褐色, 澄明の液体 | 溶解性 | 水に微溶。エタノール, アセトンに易溶。エタノール及びアセトンに極めて溶けやすく、水に溶けにくい。エタノール、エーテル、ベンゼンに可溶。リグロインに不溶。 | 用途 | トリフェニルメタン系酸性染料の中間体。 | 使用上の注意 | アルゴン封入 | 化学的特性 | clear pale yellow to yellow liquid | 使用 | 3-Methoxybenzaldehyde is used to prepare 3-(3-methoxy-phenyl)-1-phenyl-propenone by reaction with benzldehyde. It is used as an eluent for mono-13C isotopomers of vanillin in normal phase silica gel chromatography. It acts as an inhibitor of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) metabolism. | 定義 | ChEBI: 3-methoxybenzaldehyde is a member of the class of benzaldehydes in which the hydrogen at position 3 of benzaldehyde has been replaced by a methoxy group. It has a role as a Brassica napus metabolite. It is a member of benzaldehydes and a monomethoxybenzene. | Synthesis Reference(s) | Synthetic Communications, 24, p. 2011, 1994 DOI: 10.1080/00397919408010209 | 一般的な説明 | m-Anisaldehyde has significant antifungal activity against Candida sp., including the azole-resistant strains. | 安全性プロファイル | Mutation data reported. Whenheated to decomposition it emits acrid smoke andirritating vapors. | 純化方法 | Wash it with saturated aqueous NaHCO3, then H2O, dry it with anhydrous MgSO4 and distil it under reduced pressure under N2. Store it under N2 in sealed glass ampoules. [Beilstein 8 IV 241.] |
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