推薦產品
化驗
98%
折射率
n20/D 1.503 (lit.)
bp
179-180 °C (lit.)
密度
1.808 g/mL at 25 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
CCOC(=O)CI
InChI
1S/C4H7IO2/c1-2-7-4(6)3-5/h2-3H2,1H3
InChI 密鑰
MFFXVVHUKRKXCI-UHFFFAOYSA-N
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應用
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.
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 2 Oral - Eye Dam. 1 - Skin Corr. 1B
儲存類別代碼
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
170.6 °F - closed cup
閃點（°C）
77 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。
客戶也查看了
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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