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质量水平
检测方案
≥97.0% (GC)
形式
liquid
反应适用性
reaction type: C-C Bond Formation
折射率
n20/D 1.434
bp
86-87 °C/0.02 mmHg (lit.)
密度
1.131 g/mL at 20 °C (lit.)
SMILES字符串
COP(=O)(CC(=O)OC(C)(C)C)OC
InChI
1S/C8H17O5P/c1-8(2,3)13-7(9)6-14(10,11-4)12-5/h6H2,1-5H3
InChI key
SAZYDWOWLRDDRQ-UHFFFAOYSA-N
应用
Reactant for:
- Preparation of phosphonate terminated PPH dendrimers as anti-HIV-1 agents
- Preparation of monodehydro diketopiperazines from ketoacyl amino acid amides via acid-catalyzed cyclization
- Preparation of α,β-unsaturated esters for use in the guanidine-catalyzed oxa-Michael addition
- Preparation of myxopyronin B and desmethyl myxopyronin B analogs, with antibacterial activity and inhibitory activity against bacterial RNA polymerase
- Allylation and subsequent ring-closing metathesis in presence of Grubbs′ catalyst or intramolecular rhodium-catalyzed cyclopropanation reactions
其他说明
Horner-Wittig 试剂,优先生成 (E)-α,β-不饱和酯,这种酯可与酸发生轻度皂化反应。也可用于通过还原烷基化反应合成衍生物
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
A novel synthesis of (+/-)-vermiculine.
Journal of the American Chemical Society, 99(2), 646-647 (1977-01-19)
Journal of the Chemical Society. Perkin Transactions 1, 905-905 (1984)
The Journal of Organic Chemistry, 51, 956-956 (1986)
Journal of the American Chemical Society, 109, 5013-5013 (1987)
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