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Merck
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重要文件

180351

Sigma-Aldrich

2-茚醇

99%

同義詞:

2-羟基茚满

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About This Item

經驗公式(希爾表示法):
C9H10O
CAS號碼:
分子量::
134.18
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

99%

形狀

solid

mp

68-71 °C (lit.)

官能基

hydroxyl

SMILES 字串

OC1Cc2ccccc2C1

InChI

1S/C9H10O/c10-9-5-7-3-1-2-4-8(7)6-9/h1-4,9-10H,5-6H2

InChI 密鑰

KMGCKSAIIHOKCX-UHFFFAOYSA-N

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一般說明

2-Indanol is stabilized by internal hydrogen bonding in its most stable form. The resonantly enhanced multiphoton ionization (REMPI) and zero kinetic energy (ZEKE) photoelectron spectroscopy of 2-indanol was studied.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Abdulaziz A Al-Saadi et al.
The journal of physical chemistry. A, 110(44), 12292-12297 (2006-11-03)
2-Indanol in its most stable form is stabilized by internal hydrogen bonding, which exists between the hydroxyl hydrogen atom and the pi-cloud of the benzene ring. A comprehensive ab initio calculation using the MP2/cc-pVTZ level of theory showed that 2-indanol
Yonggang He et al.
The Journal of chemical physics, 124(20), 204306-204306 (2006-06-16)
We report studies of a supersonically cooled 2-indanol using two-color resonantly enhanced multiphoton ionization (REMPI) and two-color zero kinetic energy (ZEKE) photoelectron spectroscopy. In the REMPI experiment, we have identified three conformers of 2-indanol and assigned the vibrational structures of
Giuliana Donadio et al.
PloS one, 10(4), e0124427-e0124427 (2015-04-29)
Monocyclic phenols and catechols are important antioxidant compounds for the food and pharmaceutic industries; their production through biotransformation of low-added value starting compounds is of major biotechnological interest. The toluene o-xylene monooxygenase (ToMO) from Pseudomonas sp. OX1 is a bacterial

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