114278
(2-氯乙氧基)苯
98%
别名:
β-氯苯乙醚, 2-氯乙基苯基醚
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线性分子式:
C6H5OCH2CH2Cl
化学文摘社编号:
分子量:
156.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-757-0
Beilstein/REAXYS Number:
971048
MDL number:
Assay:
98%
InChI key
VQUYNUJARXBNPK-UHFFFAOYSA-N
InChI
1S/C8H9ClO/c9-6-7-10-8-4-2-1-3-5-8/h1-5H,6-7H2
SMILES string
ClCCOc1ccccc1
assay
98%
refractive index
n20/D 1.534 (lit.)
bp
97-98 °C/15 mmHg (lit.)
density
1.129 g/mL at 25 °C (lit.)
functional group
chloro, phenoxy
Quality Level
Application
(2-Chloroethoxy)benzene is used in the coupling reaction of benzaldehyde, cinnamyltrimethylsilane and anisole in the synthesis of pseudo-symmetrical tamoxifen derivatives.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
213.8 °F - closed cup
flash_point_c
101 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Isamu Shiina et al.
Bioorganic & medicinal chemistry letters, 17(9), 2421-2424 (2007-03-10)
Three new pseudo-symmetrical tamoxifen derivatives, RID-B (15), C (16), and D (17), were synthesized via the novel three-component coupling reaction, and the structure-activity relationships of the pseudo-symmetrical tamoxifen derivatives were examined. It was discovered that 15 strongly inhibits the viability
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