推荐产品
质量水平
检测方案
98%
形式
liquid
折射率
n20/D 1.595 (lit.)
bp
181-182 °C (lit.)
mp
−5-−3 °C (lit.)
溶解性
organic solvents: miscible
water: insoluble
密度
0.996 g/mL at 25 °C (lit.)
储存温度
2-8°C
SMILES字符串
C1C=Cc2ccccc12
InChI
1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2
InChI key
YBYIRNPNPLQARY-UHFFFAOYSA-N
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一般描述
通过 恶臭假单胞菌 和 红球菌 将茚氧化为 顺式 -和 反式 -茚满二醇及相关代谢产物的混合物。
应用
茚用于合成新的 C 60 衍生物茚-C 60 双加合物 。在 CH 2 Cl 2 中,用甲基异丙醚/TiCl 4 引发控制阳离子聚合制备聚茚。
警示用语:
Danger
危险声明
危险分类
Asp. Tox. 1 - Flam. Liq. 3
WGK
WGK 3
闪点(°F)
closed cup
闪点(°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
High glass transition temperature polyolefins obtained by the catalytic hydrogenation of polyindene.
Macromolecules, 36(1), 71-76 (2003)
Metabolic engineering, 1(1), 63-74 (2000-08-10)
Indene is oxidized to mixtures of cis- and trans-indandiols and related metabolites by Pseudomonas putida and Rhodococcus sp. isolates. Indene metabolism is consistent with monooxygenase and dioxygenase activity. P. putida resolves enantiomeric mixtures of cis-1,2-indandiol by further selective oxidation of
Journal of medicinal chemistry, 52(3), 675-687 (2009-01-23)
Scaffold selection involving an indole-to-indene core change led to the discovery of a series of indenylsulfonamides that act as 5-HT6 serotonin receptor agonists. The variety of the targeted ligands and their synthetic complexity required multistep synthetic approaches. The novel indenylsulfonamides
The Journal of organic chemistry, 76(9), 3551-3556 (2011-03-12)
Various fullerene-based electron acceptor materials for organic photovoltaic applications were prepared via [3+2] and [4+2] cycloadditions using a continuous flow approach. The 1,3-dipolar cycloaddition of the tosylhydrazone precursor and the Diels-Alder cycloaddition of indene to either C(60) or C(70) under
Organic & biomolecular chemistry, 8(24), 5661-5673 (2010-10-12)
Prompted by our discovery of a new class of conformationally-locked indeno[2,1-c]quinolines as anti-mycobacterials, compounds 2a and 3a (Fig. 1; MIC < 0.39 μg mL(-1) and 0.78 μg mL(-1), respectively)(14) with a freely rotating C2-imidazolo substituent, we herein describe the synthesis
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