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Merck

779202

Sigma-Aldrich

Óxido de etileno solution

2.5-3.3 M in THF

Sinónimos:

Dimethylene oxide, Epoxyethane, Ethyleneoxy, Oxacyclopropane, Oxidoethane

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About This Item

Fórmula empírica (notación de Hill):
C2H4O
Número de CAS:
Peso molecular:
44.05
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

form

solution

reaction suitability

reaction type: C-C Bond Formation

concentration

2.5-3.3 M in THF

SMILES string

C1CO1

InChI

1S/C2H4O/c1-2-3-1/h1-2H2

InChI key

IAYPIBMASNFSPL-UHFFFAOYSA-N

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Application

Ethylene oxide solution can be used for the conversion of ortho-carborane to (2′-hydroxyethyl)-1,2-dicarba-closo-dodecaborane, a key step in the synthesis of ortho-carborane-modified N-alkyl-deoxynojirimycin (DNMs).

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Eye Dam. 1 - Flam. Liq. 2 - Muta. 1B - Repr. 1B - Skin Corr. 1 - STOT RE 1 - STOT SE 3

target_organs

Central nervous system, Nervous system, Respiratory system

supp_hazards

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

1.4 °F

flash_point_c

-17 °C


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ortho?Carborane?Modified N?Substituted Deoxynojirimycin.
Hoogendoorn S
European Journal of Organic Chemistry, 2015(20), 4437-4446 (2015)
Faisal I Khan et al.
Journal of hazardous materials, 108(3), 147-159 (2004-05-04)
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V E Walker et al.
Mutation research, 233(1-2), 151-164 (1990-11-01)
The results of efforts to identify and quantify macromolecular adducts of ethylene oxide (ETO), to determine the source and significance of background levels of these adducts, and to generate molecular dosimetry data on these adducts are reviewed. A time-course study
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International journal of pharmaceutics, 440(1), 3-12 (2012-07-24)
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Caught in the oxirane: Naphthalene diimides conjugated to a quinone methide and an oxirane have been synthesized and investigated as selective DNA G-quadruplex alkylating agents. The oxirane derivative generates a stable adduct with a G-quadruplex and shows selective alkylation of

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