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About This Item
经验公式（希尔记法）:
C5H7BrO2
CAS号:
分子量:
179.01
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
97%
表单
liquid
折射率
n20/D 1.493 (lit.)
密度
1.627 g/mL at 25 °C (lit.)
官能团
bromo
ester
SMILES字符串
CC1CC(Br)C(=O)O1
InChI
1S/C5H7BrO2/c1-3-2-4(6)5(7)8-3/h3-4H,2H2,1H3
InChI key
FLOKBGAYTGLYGR-UHFFFAOYSA-N
应用
α-Bromo-γ-valerolactone was used in the synthesis of α-(2-ethoxythiocarbonylthio)-γ-valerolactone.
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
靶器官
Respiratory system
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
Paul E Reyes-Gutiérrez et al.
Organic & biomolecular chemistry, 7(7), 1388-1396 (2009-03-21)
A two-step protocol for the synthesis of azepino[4,5-b]indolone derivatives featuring a xanthate radical oxidative aromatic substitution on the N-Boc protected tryptamine, using dilauroyl peroxide (DLP) as initiator and oxidant, is described.
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