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114278

(2-氯乙氧基)苯

Name: (2-氯乙氧基)苯
Brand: ALDRICH

98%

别名:

β-氯苯乙醚, 2-氯乙基苯基醚

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关于此项目

线性分子式:

C₆H₅OCH₂CH₂Cl

化学文摘社编号:

622-86-6

分子量:

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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属性

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

说明

Application

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

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

0000485010

0000369659

0000233394

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Synthesis of the new pseudo-symmetrical tamoxifen derivatives and their anti-tumor activity.

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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货号	GTIN
114278-10ML	04061837005251