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292206

Sigma-Aldrich

2-Methyl-1,3-dioxolan

97%

Synonym(e):

Acetaldehyd-ethylenacetal

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About This Item

Empirische Formel (Hill-System):
C4H8O2
CAS-Nummer:
497-26-7
Molekulargewicht:
88.11
Beilstein:
102520
EG-Nummer:
207-841-4
MDL-Nummer:
MFCD00003210
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24857568
NACRES:
NA.22

Qualitätsniveau

100

Assay

97%

Brechungsindex

n20/D 1.398 (lit.)

bp

82-83 °C (lit.)

Dichte

0.982 g/mL at 25 °C (lit.)

Funktionelle Gruppe

ether

SMILES String

CC1OCCO1

InChI

1S/C4H8O2/c1-4-5-2-3-6-4/h4H,2-3H2,1H3

InChIKey

HTWIZMNMTWYQRN-UHFFFAOYSA-N

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Allgemeine Beschreibung

The kinetics and mechanism of the gas-phase thermal decomposition of 2-methyl-1,3-dioxolane has been studied in a static system. The infrared spectra of solid, liquid and gaseous 2-methyl-1,3-dioxolane has been studied. Low-temperature ozonation of 2-methyl-1,3-dioxolane in acetone-d6, methyl acetate and tert-butyl methyl ether has been reported.

Piktogramme

Flame
GHS02

Signalwort

Danger

H-Sätze

H225

Gefahreneinstufungen

Flam. Liq. 2

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

28.4 °F - closed cup

Flammpunkt (°C)

-2 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCQ3944
MKCN3402
MKCL3102
MKCJ9272
MKCH1660

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2-Methylaminomethyl-1,3-dioxolan 98%

Sigma-Aldrich

279749

2-Methylaminomethyl-1,3-dioxolan

T R Ward et al.
Toxicology and applied pharmacology, 122(2), 300-307 (1993-10-01)
Some compounds that inhibit acetylcholinesterase (AChE) activity compete directly with quinuclidinyl benzilate (QNB) binding, a muscarinic antagonist which binds to all subtypes equally, and with cis-methyldioxolane (CD), an agonist that binds with high affinity to the M2 subtype of muscarinic
S Yamada et al.
Brain research, 410(2), 212-218 (1987-05-05)
To study the role of central cholinergic mechanisms in hypertension, we have determined nicotinic and muscarinic agonist binding sites in the brain regions of stroke-prone spontaneously hypertensive rats (SHRSP), using [3H]nicotine and [3H]cismethyldioxolane (CD). There was a significant decrease in
H Tecle et al.
Life sciences, 52(5-6), 505-511 (1993-01-01)
The synthesis of a series of potent and efficacious 1-azabicyclo[2.2.1]heptan-3-one oxime muscarinic agonists is described. The oximes have extended appendages designed to span the cavity defined by the seven transmembrane helices of the muscarinic receptor. Some members of the series
T W Vickroy et al.
Federation proceedings, 43(13), 2785-2790 (1984-10-01)
The binding of agonists to muscarinic cholinergic receptors is well described by a binding model of multiple affinity states (superhigh, high, and low) in most central and peripheral tissues. Although previous studies of the influences by divalent cations, guanine nucleotides
T R Ward et al.
Brain research bulletin, 39(1), 49-55 (1996-01-01)
Recent reports indicate that organophosphate insecticides, in addition to inhibiting acetylcholinesterase activity, can bind directly at a subset of muscarinic receptors, which also bind cis-methyldioxolane with high affinity. Muscarinic receptors are known to act through at least two second messenger
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