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经验公式(希尔记法):
C9H10
化学文摘社编号:
分子量:
118.18
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
207-814-7
Beilstein/REAXYS Number:
1904376
MDL number:
产品名称
茚满, analytical standard
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
grade
analytical standard
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
refractive index
n20/D 1.537 (lit.)
bp
176 °C (lit.)
mp
−51 °C (lit.)
density
0.965 g/mL at 25 °C (lit.)
application(s)
environmental
format
neat
Quality Level
Gene Information
human ... CYP1A2(1544)
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
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
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
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
Manoranjan Adak et al.
Nepal Medical College journal : NMCJ, 8(1), 22-26 (2006-07-11)
To study the hyoplipidemic activity of non-methoxy and methoxy substituted--alkyl indan acetic acids in normogenic and hypergenic animal models. The hyoplipidemic activity was evaluated using normogenic and hypergenic rat models. Indan acids synthesized in our laboratory (50 mg/kg) and the
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