180351
2-Indanol
99%
Sinônimo(s):
2-Hydroxyindan
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About This Item
Fórmula empírica (Notação de Hill):
C9H10O
Número CAS:
Peso molecular:
134.18
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Formulário:
solid
Ensaio:
99%
Produtos recomendados
Ensaio
99%
Formulário
solid
pf
68-71 °C (lit.)
grupo funcional
hydroxyl
cadeia de caracteres SMILES
OC1Cc2ccccc2C1
InChI
1S/C9H10O/c10-9-5-7-3-1-2-4-8(7)6-9/h1-4,9-10H,5-6H2
chave InChI
KMGCKSAIIHOKCX-UHFFFAOYSA-N
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Descrição geral
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.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
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
The Toluene o-Xylene Monooxygenase Enzymatic Activity for the Biosynthesis of Aromatic Antioxidants.
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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