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化驗
99%
折射率
n20/D 1.425 (lit.)
bp
139-140 °C (lit.)
密度
0.829 g/mL at 25 °C (lit.)
SMILES 字串
CC(C)C(O)C(C)C
InChI
1S/C7H16O/c1-5(2)7(8)6(3)4/h5-8H,1-4H3
InChI 密鑰
BAYAKMPRFGNNFW-UHFFFAOYSA-N
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應用
2,4-二甲基-3-戊醇用作与 2-取代丙烯酸酯衍生物的非对映选择性偶联的质子源。它用于 1,1′-(1,3-亚苯基)二乙醇(1,3-二醇)和己二酸二异丙酯的聚合反应。
訊號詞
Danger
危險分類
Acute Tox. 4 Oral - Eye Dam. 1 - 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)
98.6 °F - closed cup
閃點(°C)
37 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Organic letters, 11(4), 879-882 (2009-01-28)
A mild, stereoselective method for the Ni-catalyzed synthesis of alpha-C-alkylglycosides is reported. This approach entails the reductive coupling of glycosyl bromides with activated alkenes at room temperature, with low alkene loading as an important feature. Diastereoselective coupling with 2-substituted acrylate
Chemistry (Weinheim an der Bergstrasse, Germany), 13(29), 8325-8332 (2007-07-31)
The well-known dynamic kinetic resolution of secondary alcohols and esters was extended to secondary diols and diesters to afford chiral polyesters. This process is an example of iterative tandem catalysis (ITC), a polymerization method where the concurrent action of two
Scientific reports, 9(1), 18067-18067 (2019-12-04)
Camptothecin (CPT), a natural alkaloid isolated from Camptotheca acuminata Decne, is found to show potential insecticidal activities with unique action mechanisms by targeting at DNA-topoisomease I (Top1) complex and inducing cell apoptosis. To improve the efficacy against insect pests, two
Pesticide biochemistry and physiology, 139, 46-52 (2017-06-10)
Camptothecin (CPT), a quinolone alkaloid extracted from Camptotheca acuminata Decne, exhibits potential insecticidal activities against various insect species. Our previous studies have showed that CPT induced apoptosis in Spodoptera exigua Hübner cell line and inhibited the relaxation activity of topoisomerase
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