推荐产品
质量水平
方案
97%
折射率
n20/D 1.398 (lit.)
沸点
82-83 °C (lit.)
密度
0.982 g/mL at 25 °C (lit.)
官能团
ether
SMILES字符串
CC1OCCO1
InChI
1S/C4H8O2/c1-4-5-2-3-6-4/h4H,2-3H2,1H3
InChI key
HTWIZMNMTWYQRN-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
一般描述
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。
警示用语：
Danger
危险声明
危险分类
Flam. Liq. 2
储存分类代码
3 - Flammable liquids
WGK
WGK 2
闪点(°F)
28.4 °F - closed cup
闪点(°C)
-2 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
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
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
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
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
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
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门