质量水平
方案
95%
表单
liquid
折射率
n20/D 1.537 (lit.)
沸点
176 °C (lit.)
mp
−51 °C (lit.)
密度
0.965 g/mL at 25 °C (lit.)
SMILES字符串
C1Cc2ccccc2C1
InChI
1S/C9H10/c1-2-5-9-7-3-6-8(9)4-1/h1-2,4-5H,3,6-7H2
InChI key
PQNFLJBBNBOBRQ-UHFFFAOYSA-N
基因信息
human ... CYP1A2(1544)
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警示用语：
Danger
危险声明
危险分类
Asp. Tox. 1 - Flam. Liq. 3
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
129.2 °F - closed cup
闪点(°C)
54 °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
此项目有
Wei Li et al.
Chemical communications (Cambridge, England), 46(22), 3979-3981 (2010-04-22)
(S,R)-Indan-ambox ligand and its ruthenium(II) complex have been prepared and successfully applied to asymmetric hydrogenation of prochiral simple ketones. A wide range of unfunctionalized ketones are reduced by Ru(II)-indan-ambox catalyst with excellent enantioselectivities (up to 97% ee).
Kenji Kabashima et al.
FEBS letters, 578(1-2), 36-40 (2004-12-08)
Nuclear factor kappa B (NF-kappaB) plays a wide variety of pathophysiological roles and modulation of its pathway can be a good novel drug target. Here, we found that our recently synthesized NF-kappaB inhibitor attenuated an ovalbumin-specific delayed-type hypersensitivity response in
Mónica López-García et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 10(12), 3006-3014 (2004-06-24)
The efficient chemoenzymatic synthesis of enantiopure 1,3-difunctionalized indane derivatives has been achieved. The corresponding cis and trans N-protected amino alcohols were successfully resolved by acetylation using lipase B, which is a biocatalyst isolated from Candida antarctica. All the possible isomers
G Bieniek
Journal of chromatography. A, 891(2), 361-365 (2000-10-24)
An attempt was made to establish a method for the simultaneous determination of ethylbenzene, indan, indene and acenaphthene by capillary gas chromatography with flame ionization detection. The air was sampled on charcoal tubes and extracted with carbon disulfide-methanol (60:1, v/v).
Yuka Kobayashi et al.
Chirality, 17(2), 108-112 (2005-01-22)
Both novel enantiopure trans-1-aminobenz[f]indan-2-ols (4) were obtained from the racemate by the diastereomeric salt formation with (+)- and (-)-dibenzoyltartaric acids (8), respectively, and the absolute configuration of the enantiomer 4 in the less-soluble diastereomeric salt of racemic 4 with (+)-8
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