추천 제품
Quality Level
분석
98%
refractive index
n20/D 1.503 (lit.)
bp
179-180 °C (lit.)
density
1.808 g/mL at 25 °C (lit.)
작용기
ester
iodo
저장 온도
2-8°C
SMILES string
CCOC(=O)CI
InChI
1S/C4H7IO2/c1-2-7-4(6)3-5/h2-3H2,1H3
InChI key
MFFXVVHUKRKXCI-UHFFFAOYSA-N
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일반 설명
Ethyl iodoacetate, also known as iodoacetic acid ethyl ester, serves as an alkylating agent and a radical precursor in organic synthesis. It is also commonly used as a lachrymatory agent.
애플리케이션
Ethyl iodoacetate was used in the synthesis of trans-2,3-disubstituted indolines by reacting with 1-azido-2-allylbenzene derivatives via a diastereoselective radical cascade.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 2 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
170.6 °F - closed cup
Flash Point (°C)
77 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
François Brucelle et al.
The Journal of organic chemistry, 78(12), 6245-6252 (2013-06-01)
The preparation of trans-2,3-disubstituted indolines from 1-azido-2-allylbenzene derivatives via a diastereoselective radical cascade using ethyl iodoacetate and triethylborane is described. Further lactamization afforded substituted benzopyrrolizidinones with excellent diastereomeric ratios. The radical cascade/lactamization sequence was efficiently applied to the synthesis of
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