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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:
622-86-6
Molecular Weight:
156.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847162
EC Number:
210-757-0
Beilstein/REAXYS Number:
971048
MDL number:
MFCD00018946
Assay:
98%
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Quality Level

200

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

Application

(2-Chloroethoxy)benzene is used in the coupling reaction of benzaldehyde, cinnamyltrimethylsilane and anisole in the synthesis of pseudo-symmetrical tamoxifen derivatives.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000485010
0000485010
0000369659
0000369659
0000233394

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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

Global Trade Item Number

SKUGTIN
114278-10ML04061837005251