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Merck
CN

368210

Ethyl 2-(trimethylsilylmethyl)acrylate

97%

Synonym(s):

2-(Trimethylsilylmethyl)acrylic acid ethyl ester, Ethyl 2-(trimethylsilylmethyl)propenoate

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About This Item

Linear Formula:
H2C=C[CH2Si(CH3)3]CO2C2H5
CAS Number:
Molecular Weight:
186.32
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4658894
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assay

97%

InChI

1S/C9H18O2Si/c1-6-11-9(10)8(2)7-12(3,4)5/h2,6-7H2,1,3-5H3

SMILES string

CCOC(=O)C(=C)C[Si](C)(C)C

InChI key

HSEYTIDQGJXPIF-UHFFFAOYSA-N

form

liquid

bp

70-72 °C/10 mmHg (lit.)

density

0.897 g/mL at 25 °C (lit.)

storage temp.

2-8°C

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 3

flash_point_f

141.8 °F - closed cup

flash_point_c

61 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Synthesis of Carbohydrate Derived a-Methylene-?-lactones by Diasterecseldctive, Low Temperature Reformatsky-Type Reactions.
Csuk R, et al.
Journal of Carbohydrate Chemistry, 5(3), 459- 467 (1986)
Synthesis of Carbohydrate Derived ?-Methylene-?-lactones by Diasterecseldctive, Low Temperature Reformatsky-Type Reactions
Csuk R, et al.
Journal of Carbohydrate Chemistry, 5(3), 459-467 (1986)

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