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Merck
CN

374520

三氯甲基膦酸二乙酯

97%

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线性分子式:
(CH3CH2O)2P(O)CCl3
化学文摘社编号:
分子量:
255.46
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1210640
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assay

97%

form

liquid

InChI

1S/C5H10Cl3O3P/c1-3-10-12(9,11-4-2)5(6,7)8/h3-4H2,1-2H3

SMILES string

CCOP(=O)(OCC)C(Cl)(Cl)Cl

InChI key

RVAQSYWDOSHWGP-UHFFFAOYSA-N

bp

130-131 °C/14 mmHg (lit.)

density

1.362 g/mL at 25 °C (lit.)

storage temp.

2-8°C

General description

Addition reaction of diethyl (trichloromethyl)phosphonate to olefins by non-chain catalytic reactions catalyzed by copper amine complexes has been reported. Irradiation of diethyl (trichloromethyl)phosphonate in MeCN is reported to afford corresponding monoesters and olefins, via photochemical type II elimination reaction.

Application

Diethyl (trichloromethyl)phosphonate may be used in the synthesis of chlorovinyl phosphonates via reaction with aldehydes and ketones.

pictograms

Exclamation mark

signalword

Warning

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

235.4 °F - closed cup

flash_point_c

113 °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

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A novel synthesis of phosphonates from diethyl (trichloromethyl) phosphonate.
Lowen GT and Almond MR.
The Journal of Organic Chemistry, 59(!6), 4548-4550 (1994)
Addition of diethyl trichloromethylphosphonate to olefins catalysed by copper complexes.
Villemin D, et al.
Tetrahedron Letters, 35(21), 3537-3538 (1994)
Photochemical type I and II elimination reactions of dialkyl (trichloromethyl) phosphonates.
Suzuki N, et al.
Bulletin of the Chemical Society of Japan, 53(5), 1421-1424 (1980)

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