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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

Quality Level

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)
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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)
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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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