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Merck
CN

263699

3-Ethoxyacrylonitrile, mixture of cis and trans

97%

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About This Item

Linear Formula:
C2H5OCH=CHCN
CAS Number:
Molecular Weight:
97.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
262-706-7
MDL number:
Assay:
97%
Form:
liquid
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InChI key

HUPVIAINOSTNBJ-UHFFFAOYSA-N

InChI

1S/C5H7NO/c1-2-7-5-3-4-6/h3,5H,2H2,1H3

SMILES string

CCOC=CC#N

assay

97%

form

liquid

refractive index

n20/D 1.454 (lit.)

bp

90-91 °C/19 mmHg (lit.)

density

0.944 g/mL at 25 °C (lit.)

functional group

ether, nitrile

General description

Heck reaction of 3-ethoxyacrylonitrile with aryl bromides catalyzed by a tetraphosphine/palladium complex has been reported.

Application

3-Ethoxyacrylonitrile has been used in the preparation of (Z)-β-aminoacrylonitrile.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

179.6 °F - closed cup

flash_point_c

82 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Heck reactions of 2-substituted enol ethers with aryl bromides catalysed by a tetraphosphine/palladium complex.
Battace A, et al.
Tetrahedron Letters, 47(4), 459-462 (2006)
Sundeep Rayat et al.
Chemical research in toxicology, 18(8), 1211-1218 (2005-08-16)
A discussion of nitrosative deamination of cytosine 1 is presented that argues for the formation of 6 by diazotization of 1 to cytosinediazonium ion 2 and its electrostatic complex 3, dediazoniation to 4 <--> 5, and amide-bond cleavage to 6.

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