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114278

Sigma-Aldrich

(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
Beilstein:
971048
EC Number:
210-757-0
MDL number:
MFCD00018946
UNSPSC Code:
12352100
PubChem Substance ID:
24847162
NACRES:
NA.22

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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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Certificates of Analysis (COA)

Lot/Batch Number
0000369659
0000369659
0000233394
BGBB9363

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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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