193739
1-茚醇
98%
别名:
(±)-1-茚醇, (±)-1-羟基茚满
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关于此项目
经验公式（希尔记法）:
C9H10O
化学文摘社编号:
分子量:
134.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
228-755-3
Beilstein/REAXYS Number:
2042960
MDL number:
产品名称
1-茚醇, 98%
InChI key
YIAPLDFPUUJILH-UHFFFAOYSA-N
InChI
1S/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2
SMILES string
OC1CCc2ccccc12
assay
98%
form
solid
bp
128 °C/12 mmHg (lit.)
mp
50-54 °C (lit.)
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General description
1-茚满醇的手性敏感聚集已通过FTIR光谱进行了研究。已经使用环己烯作为氢受体在非均相钯催化剂上对1-茚满醇的转移脱氢进行了研究。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Wanda Mączka et al.
Molecules (Basel, Switzerland), 24(23) (2019-12-01)
The main purpose of this publication was to obtain the S-enantiomer of indan-1-ol with high enantiomeric excess and satisfactory yield. In our research, we used carrot callus cultures (Daucuscarota L.), whereby the enzymatic system reduced indan-1-one and oxidized indan-1-ol. During
Jonas Altnöder et al.
Physical chemistry chemical physics : PCCP, 15(25), 10167-10180 (2013-05-15)
The aggregation behavior of racemic and enantiopure 1-indanol has been studied by FTIR spectroscopy, resonant ion dip IR spectroscopy, and spontaneous Raman scattering in supersonic jets. This triple experimental approach, augmented by homology to related molecular fragments and dispersion-corrected DFT
Selective transfer dehydrogenation of aromatic alcohols on supported palladium.
Keresszegi C, et al.
New. J. Chem., 25(9), 1163-1167 (2001)
Ticiane C de Souza et al.
Bioprocess and biosystems engineering, 43(12), 2253-2268 (2020-07-30)
In this study, the modulation of enzymatic biocatalysts were developed by the use of lipase B from Candida antarctica covalently immobilized on an eco-friendly support, cashew apple bagasse, activated with 10% glycidol-ethylenediamine-glutaraldehyde (GEG) under different immobilization strategies (5 mM or 100 mM
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
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