所有图片(2)
About This Item
经验公式（希尔记法）:
C9H10O
CAS号:
分子量:
134.18
Beilstein:
4350388
MDL编号:
UNSPSC代码:
12352002
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
99%
旋光性
[α]30/D −29°, c = 2 in chloroform
mp
72-73 °C (lit.)
官能团
hydroxyl
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-/m1/s1
InChI key
YIAPLDFPUUJILH-SECBINFHSA-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
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
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
Gustaf Götmar et al.
Analytical chemistry, 76(1), 197-202 (2003-12-31)
The distributions of the adsorption energies (AED) of two enantiomers, (R)-1- indanol and (S)-1-indanol, on a chiral stationary phase were measured and the results are discussed. The chiral phase used is made of cellulose tribenzoate coated on porous silica. The
J Reddy et al.
Applied microbiology and biotechnology, 51(5), 614-620 (1999-07-03)
Recombinant Escherichia coli cells expressing the toluene dioxygenase (TDO) genes from Pseudomonas putida convert indene to cis-1S,2R-indandiol, a potentially important intermediate for the chemical synthesis of the HIV-1 protease inhibitor, Crixivan. A bioconversion process was developed through optimization of medium
D T Gibson et al.
Journal of bacteriology, 177(10), 2615-2621 (1995-05-01)
The stereospecific oxidation of indan and indene was examined with mutant and recombinant strains expressing naphthalene dioxygenase of Pseudomonas sp. strain 9816-4. Pseudomonas sp. strain 9816/11 and Escherichia coli JM109(DE3)[pDTG141] oxidized indan to (+)-(1S)-indanol, (+)-cis-(1R,2S)-indandiol, (+)-(1S)-indenol, and 1-indanone. The same
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