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About This Item
经验公式（希尔记法）:
C9H10O
CAS号:
分子量:
134.18
Beilstein:
2206709
MDL编号:
UNSPSC代码:
12352002
PubChem化学物质编号:
NACRES:
NA.22
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方案
99%
旋光性
[α]20/D +30°, c = 2 in chloroform
mp
69-73 °C (lit.)
SMILES字符串
O[C@H]1CCc2ccccc12
InChI
1S/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2/t9-/m0/s1
InChI key
YIAPLDFPUUJILH-VIFPVBQESA-N
基因信息
human ... UGT2B17(7367) , UGT2B7(7364)
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警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Katia Le Barbu-Debus et al.
Physical chemistry chemical physics : PCCP, 20(21), 14635-14646 (2018-05-18)
The influence of flexibility and hydrogen bond formation on the IR absorption and vibrational circular dichroism (VCD) spectrum of a floppy protic molecule, namely, (S)-1-indanol, is studied in both non-polar CCl4 and polar DMSO solvents. The experimental IR absorption and
K Lee et al.
Applied and environmental microbiology, 63(5), 2067-2070 (1997-05-01)
A recombinant Escherichia coli strain which expresses naphthalene dioxygenase (NDO) from Pseudomonas sp. strain NCIB 9816-4 oxidized (S)-1-indanol to trans-(1S,3S)-indan-1,3-diol (95.5%) and (R)-3-hydroxy-1-indanone (4.5%). The same cells oxidized (R)-1-indanol to cis-1,3-indandiol (71%), (R)-3-hydroxy-1-indanone (18.2%), and cis-1,2,3-indantriol (10.8%). Purified NDO oxidized
Conformational landscapes and free-jet rotational spectrum of indan-1-ol.
Biagio Velino et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 7(3), 565-568 (2006-02-14)
Y Miyabe et al.
Biological & pharmaceutical bulletin, 18(1), 9-12 (1995-01-01)
We have investigated the steady-state kinetics for a cytosolic 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase isozyme of human liver and its inhibition by several bile acids and anti-inflammatory drugs such as indomethacin, flufemanic acid and naproxen. Initial velocity and product inhibition studies performed
Attila Felinger et al.
Journal of chromatography. A, 1005(1-2), 35-49 (2003-08-20)
The inverse method of isotherm determination consists in calculating the numerical values of the coefficients of an isotherm model that give a set of chromatographic profiles in best possible agreement with the set of experimental profiles available. This method was
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