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239798

1,3-Dioxolane

≥99.5%

Synonym(s):

Ethylene glycol methylene ether, Formaldehyde ethylene acetal

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About This Item

Empirical Formula (Hill Notation):
C3H6O2
CAS Number:
646-06-0
Molecular Weight:
74.08
Beilstein/REAXYS Number:
102453
MDL number:
MFCD00003207
UNSPSC Code:
12352200
PubChem Substance ID:
329752533

vapor density

2.6 (vs air)

vapor pressure

70 mmHg ( 20 °C)

assay

≥99.5%

autoignition temp.

525 °F

contains

75 ppm BHT as inhibitor

refractive index

n20/D 1.401 (lit.)

bp

75-76 °C/1.013 hPa

mp

−95 °C (lit.)

density

1.06 g/mL at 25 °C (lit.)

SMILES string

C1COCO1

InChI

1S/C3H6O2/c1-2-5-3-4-1/h1-3H2

InChI key

WNXJIVFYUVYPPR-UHFFFAOYSA-N

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Certificates of Analysis (COA)

Lot/Batch Number
11020AG
00302BF
02209DZ
00506MV

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Zhenhua Sun et al.
Nature communications, 8, 14627-14627 (2017-03-04)
Although the rechargeable lithium-sulfur battery is an advanced energy storage system, its practical implementation has been impeded by many issues, in particular the shuttle effect causing rapid capacity fade and low Coulombic efficiency. Herein, we report a conductive porous vanadium
Charles A Ault et al.
Macromolecular rapid communications, 42(5), e2000692-e2000692 (2021-01-28)
Effects of molecular weight of methylphenyl-containing vinylsiloxy-functionalized terpolysiloxanes on their UV-activated crosslinking by hydrosilylation at room temperature in air, shelf life stability of "all-in-one" pastes prepared from them for additive manufacturing, and mechanical properties of the resulting crosslinked elastomers, are
Silvia Franchini et al.
European journal of medicinal chemistry, 45(9), 3740-3751 (2010-07-08)
A series of 1,3-dioxolane-based compounds incorporating a lactam (2-4) or imide (5-7) moiety was synthesized and the pharmacological profile at alpha(1)-adrenoceptor subtypes and 5-HT(1A) receptor was assessed through binding and functional experiments. Starting from the 2,2-diphenyl-1,3-dioxolane derivative 1, previously shown
One-step synthesis of 2-alkyl-dioxolanes from ethylene glycol and syngas.
Xiao-Bing Fan et al.
ChemSusChem, 2(10), 941-943 (2009-10-01)
Lukas J Goossen et al.
The Journal of organic chemistry, 73(21), 8631-8634 (2008-10-23)
An efficient synthesis of the angiotensin II receptor antagonist telmisartan is presented involving a decarboxylative cross-coupling of isopropyl phthalate (1) with 2-(4-chlorophenyl)-1,3-dioxolane (2c) as the key step (85% yield). The benzimidazole moiety is constructed regioselectively via a reductive amination-condensation sequence
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