推荐产品
等級
technical grade
化驗
85%
形狀
liquid
折射率
n20/D 1.442 (lit.)
bp
172-174 °C (lit.)
密度
0.981 g/mL at 25 °C (lit.)
SMILES 字串
CC(C(C)=O)C(C)=O
InChI
1S/C6H10O2/c1-4(5(2)7)6(3)8/h4H,1-3H3
InChI 密鑰
GSOHKPVFCOWKPU-UHFFFAOYSA-N
一般說明
据报道，过氧亚硝酸盐促进 3-甲基-2,4-戊二酮的好氧氧化。在气相中使用脉冲激光光解-激光诱导荧光技术研究了 OH 自由基与 3-甲基-2,4-戊二酮的反应动力学。3-甲基-2,4-戊二酮参与两亲树脂负载的单齿膦配体催化的 1,3-二苯基-2-丙烯基乙酸酯的不对称取代。
訊號詞
Warning
危險分類
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
134.6 °F - closed cup
閃點（°C）
57 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
F S Knudsen et al.
Chemical research in toxicology, 13(5), 317-326 (2000-05-17)
Peroxynitrite is shown here to promote the aerobic oxidation of isobutanal (IBAL) and 3-methyl-2,4-pentanedione (MP) in a pH 7.2 phosphate buffer into acetone plus formate and biacetyl plus acetate, respectively. These products are expected from dioxetane intermediates, whose thermolysis is
Rate coefficients for the reactions of OH radicals with the keto/enol tautomers of 2, 4-pentanedione and 3-methyl-2, 4-pentanedione, allyl alcohol and methyl vinyl ketone using the enols and methyl nitrite as photolytic sources of OH.
Holloway A-L, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 176(1), 183-190 (2005)
Palladium-catalyzed asymmetric allylic substitution in aqueous media using amphiphilic resin-supported MOP ligands.
Uozumi Y, et al.
Tetrahedron Letters, 39(45), 8303-8306 (1998)
Marzena Fandzloch et al.
Journal of inorganic biochemistry, 176, 144-155 (2017-09-15)
Tropical diseases currently constitute a major health problem and thus a challenge in the field of drug discovery. The current treatments show serious disadvantages due to cost, toxicity, long therapy duration and resistance, and the use of metal complexes as
Jiyuan Jin et al.
Chemosphere, 223, 628-635 (2019-02-25)
Quinones are components of electron transport chains in photosynthesis and respiration. Acetylacetone (AA), structurally similar to benzoquinone (BQ) for the presence of two identical carbonyl groups, has been reported as a quinone-like electron shuttle. Both BQ and AA are important
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