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质量水平
检测方案
≥99%
bp
220 °C (lit.)
mp
30-32 °C (lit.)
密度
1.049 g/mL at 25 °C (lit.)
储存温度
2-8°C
SMILES字符串
N#CCC#N
InChI
1S/C3H2N2/c4-2-1-3-5/h1H2
InChI key
CUONGYYJJVDODC-UHFFFAOYSA-N
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一般描述
丙二腈,一种弱氰基碳酸,是一种反应性超高的多功能化合物。这种结晶脂肪族腈可用作合成杂环化合物和聚合物的合成砌块。
应用
丙二腈可用于:
- 碱促进的[1,6]-萘啶水上合成。†
- γ--酮酰胺的合成。
- 特殊杂环药物支架(包括吡啶、1,4-二氢吡啶、苯并吡喃[2,3-b]吡啶和二氢-1,4-二噻吩骨架)的制备。
包装
玻璃瓶封装
警示用语:
Danger
危险分类
Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
危险化学品
High-Performance Quinoline-Malononitrile Core as a Building Block for the Diversity-Oriented Synthesis of AIEgens
Angewandte Chemie (International Edition in English), 59, 9812-9825 (2020)
The chemistry of malononitrile.
Chemical reviews, 69(5), 591-624 (1969-10-01)
Nature communications, 9(1), 2903-2903 (2018-07-27)
Electron transfer reactions are arguably the simplest chemical reactions but they have not yet ceased to intrigue chemists. Charge-separation and charge-recombination reactions are at the core of life-sustaining processes, molecular electronics and solar cells. Intramolecular electron donor-acceptor systems capture the
Ultrasonics sonochemistry, 19(4), 725-728 (2012-02-14)
A one-pot three-component condensation of an aldehyde, malononitrile, and resorcinol has been achieved by ultrasound method. The reaction has been catalyzed by glycine in aqueous medium. This protocol afforded corresponding 2-amino-4H-chromenes in shorter reaction times, high yields and simple work-up
Ultrasonics sonochemistry, 19(3), 491-497 (2011-11-29)
Novel fused pyrans were synthesized from the reaction of the tetrahydropyran-4-one with arylidine malononitriles. Different fused pyran derivatives were obtained from the mentioned reaction depending on type of catalyst used and type of energy used. Reactions were carried out under
商品
MOST offers controlled solar energy harvesting and storage, addressing global energy demands with improved storage techniques.
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
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