I1804
茚满
95%
别名:
二氢化茚
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关于此项目
经验公式（希尔记法）:
C9H10
化学文摘社编号:
分子量:
118.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-814-7
Beilstein/REAXYS Number:
1904376
MDL number:
产品名称
茚满, 95%
InChI key
PQNFLJBBNBOBRQ-UHFFFAOYSA-N
InChI
1S/C9H10/c1-2-5-9-7-3-6-8(9)4-1/h1-2,4-5H,3,6-7H2
SMILES string
C1Cc2ccccc2C1
assay
95%
form
liquid
refractive index
n20/D 1.537 (lit.)
bp
176 °C (lit.)
mp
−51 °C (lit.)
density
0.965 g/mL at 25 °C (lit.)
Quality Level
Gene Information
human ... CYP1A2(1544)
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signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
129.2 °F - closed cup
flash_point_c
54 °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
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
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).
Peter R Andreana et al.
Organic letters, 6(23), 4231-4233 (2004-11-05)
A catalytic asymmetric Passerini reaction using tridentate indan (pybox) Cu(II) Lewis acid complex 4 with substrates capable of bidentate coordination has been achieved. The reaction occurs via ligand-accelerated catalysis.
Naoki Tarui et al.
Bioscience, biotechnology, and biochemistry, 66(2), 464-466 (2002-05-10)
Racemic indan derivatives have been resolved by the hydrolysis of amide bonds using Corynebacterium ammoniagenes IFO12612 to produce (S)-amine and (R)-amides. In the kinetic resolution of 1 (N-12-(6-methoxy-indan-1-yl)ethyl]acetamide), it was possible to run the reaction to 44% conversion on a
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
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