추천 제품
분석
97%
refractive index
n20/D 1.429 (lit.)
bp
75-76 °C/4 mmHg (lit.)
density
0.94 g/mL at 25 °C (lit.)
작용기
carboxylic acid
SMILES string
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
일반 설명
3-Methyl-4-pentenoic acid can be synthesized from crotyl acetate via Claisen rearrangement.
애플리케이션
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
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
199.9 °F - closed cup
Flash Point (°C)
93.3 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation
Ireland ER, et al.
Journal of the American Chemical Society, 98(10), 2868-2877 (1976)
Understanding the effect of allylic methyls in olefin cross-metathesis.
Courchay FC, et al.
Journal of Organometallic Chemistry, 691(4), 585-594 (2006)
1, 2-Diferrocenylethane from an Unusual Reaction
Jr R.et al.
Journal of the American Chemical Society, 81(12), 3162-3163 (1959)
Stereoselective selenolactonization by superelectrophilic benzeneselenenyl triflate.
Murata S and Suzuki T.
Chemistry Letters (Jpn), 5, 849-852 (1987)
Back TG.
Organosilicon Chemistry, 40-40 (1999)
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