124184
α-溴-γ-戊內酯，顺式和反式混合物
97%
别名:
2-溴-4-羟基戊酸-γ-内酯
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关于此项目
经验公式（希尔记法）:
C5H7BrO2
化学文摘社编号:
分子量:
179.01
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
247-380-6
MDL number:
Assay:
97%
Form:
liquid
InChI key
FLOKBGAYTGLYGR-UHFFFAOYSA-N
InChI
1S/C5H7BrO2/c1-3-2-4(6)5(7)8-3/h3-4H,2H2,1H3
SMILES string
CC1CC(Br)C(=O)O1
assay
97%
form
liquid
refractive index
n20/D 1.493 (lit.)
density
1.627 g/mL at 25 °C (lit.)
functional group
bromo, ester
Application
α-Bromo-γ-valerolactone was used in the synthesis of α-(2-ethoxythiocarbonylthio)-γ-valerolactone.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
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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