114278
(2-Chloroethoxy)benzene
98%
Synonym(s):
β-Chlorophenetole, 2-Chloroethyl phenyl ether
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About This Item
Linear Formula:
C6H5OCH2CH2Cl
CAS Number:
Molecular Weight:
156.61
Beilstein:
971048
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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
SMILES string
ClCCOc1ccccc1
InChI
1S/C8H9ClO/c9-6-7-10-8-4-2-1-3-5-8/h1-5H,6-7H2
InChI key
VQUYNUJARXBNPK-UHFFFAOYSA-N
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Application
(2-Chloroethoxy)benzene is used in the coupling reaction of benzaldehyde, cinnamyltrimethylsilane and anisole in the synthesis of pseudo-symmetrical tamoxifen derivatives.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
213.8 °F - closed cup
Flash Point(C)
101 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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