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方案
97%
折射率
n20/D 1.429 (lit.)
沸点
75-76 °C/4 mmHg (lit.)
密度
0.94 g/mL at 25 °C (lit.)
官能团
carboxylic acid
SMILES字符串
CC(CC(O)=O)C=C
InChI
1S/C6H10O2/c1-3-5(2)4-6(7)8/h3,5H,1,4H2,2H3,(H,7,8)
InChI key
QNPZXLANENFTFK-UHFFFAOYSA-N
一般描述
3-Methyl-4-pentenoic acid can be synthesized from crotyl acetate via Claisen rearrangement.
应用
3-Methyl-4-pentenoic acid may be used to synthesize:
- trans- and cis-5-phenylseleno-3-methyl-4-pentanolides
- trans- and cis-5-iodo-3-methyl-4-pentanolides
- 3-methyl-4-pentene-1-ol
警示用语:
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
199.9 °F - closed cup
闪点(°C)
93.3 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
从最新的版本中选择一种:
分析证书(COA)
1, 2-Diferrocenylethane from an Unusual Reaction
Journal of the American Chemical Society, 81(12), 3162-3163 (1959)
The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation
Journal of the American Chemical Society, 98(10), 2868-2877 (1976)
Understanding the effect of allylic methyls in olefin cross-metathesis.
Journal of Organometallic Chemistry, 691(4), 585-594 (2006)
Stereoselective selenolactonization by superelectrophilic benzeneselenenyl triflate.
Chemistry Letters (Jpn), 5, 849-852 (1987)
Organosilicon Chemistry, 40-40 (1999)
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