292206
2-甲基-1,3-二氧戊环
97%
别名:
乙醛乙二醇缩醛
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关于此项目
经验公式（希尔记法）:
C4H8O2
化学文摘社编号:
分子量:
88.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-841-4
Beilstein/REAXYS Number:
102520
MDL number:
Assay:
97%
InChI key
HTWIZMNMTWYQRN-UHFFFAOYSA-N
InChI
1S/C4H8O2/c1-4-5-2-3-6-4/h4H,2-3H2,1H3
SMILES string
CC1OCCO1
assay
97%
Quality Level
refractive index
n20/D 1.398 (lit.)
bp
82-83 °C (lit.)
density
0.982 g/mL at 25 °C (lit.)
functional group
ether
General description
研究了静态系统中 2-甲基-1,3-二氧戊环的气相热分解的动力学和机理。研究了固体、液体和气体 2-甲基-1,3-二氧戊环的红外光谱。已报道在丙酮-d6、乙酸甲酯和叔丁基甲基醚中低温臭氧化 2-甲基-1,3-二氧戊环。
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
28.4 °F - closed cup
flash_point_c
-2 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Bozo Plesnicar et al.
Journal of the American Chemical Society, 124(38), 11260-11261 (2002-09-19)
Low-temperature ozonation (-78 degrees C) of 2-methyl-1,3-dioxolane (1a) in acetone-d6, methyl acetate, and tert-butyl methyl ether produced both the corresponding acetal hydrotrioxide (3a, ROOOH) and the hemiortho ester (2a, ROH) in molar ratio 1:5. Both intermediates were fully characterized by
E T Iwamoto et al.
The Journal of pharmacology and experimental therapeutics, 271(2), 601-608 (1994-11-01)
This study was designed to determine if the antinociception produced by intrathecally (i.t.) administered muscarinic agonists in male Sprague-Dawley rats is mediated by an L-arginine/nitric oxide/cyclic GMP cascade. Seven days after implantation of intrathecal catheters, antinociception was produced with graded
G Blanchet et al.
Comptes rendus des seances de la Societe de biologie et de ses filiales, 178(5), 526-534 (1984-01-01)
The radioreceptor assay for acetylcholine (ACh) is based on the ability of the ACh to compete with the specific binding of [3H] cis-methyldioxolane to muscarinic receptors of rat cerebral cortex membranes. The technique described was used to measure ACh levels
N Watson et al.
Journal of autonomic pharmacology, 14(4), 283-293 (1994-08-01)
1. Muscarinic receptors mediating contraction of rabbit endothelium-denuded aorta have been characterized functionally, in vitro, using a range of antagonists (atropine, pirenzepine, methoctramine, himbacine, 4-diphenyl-acetoxy-N-methyl piperidine methiodide (4-DAMP) and para-fluoro-hexahydro-siladifenidol (p-F-HHSiD). 2. The non-selective muscarinic agonist, (+)cis-dioxolane, induced concentration-dependent contractions
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
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