156019
2,4-Pentanediol
98%
Sinônimo(s):
1,3-Dimethylpropane-1,3-diol, 2,4-Amylene glycol, 2,4-Dihydroxypentane
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About This Item
Fórmula linear:
CH3CH(OH)CH2CH(OH)CH3
Número CAS:
Peso molecular:
104.15
Beilstein:
969186
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
98%
Formulário
liquid
índice de refração
n20/D 1.435 (lit.)
p.e.
201-202 °C (lit.)
densidade
0.95 g/mL at 25 °C (lit.)
grupo funcional
hydroxyl
cadeia de caracteres SMILES
CC(O)CC(C)O
InChI
1S/C5H12O2/c1-4(6)3-5(2)7/h4-7H,3H2,1-2H3
chave InChI
GTCCGKPBSJZVRZ-UHFFFAOYSA-N
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Aplicação
2,4-Pentanediol was used in the synthesis of chelated multinuclear complexes.
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
213.8 °F - closed cup
Ponto de fulgor (°C)
101.00 °C - closed cup
Equipamento de proteção individual
Eyeshields, Gloves
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Katsumasa Kamiya et al.
The journal of physical chemistry. A, 116(4), 1168-1175 (2012-01-10)
We report ab initio molecular dynamics calculations based on density functional theory performed on an intramolecular [2 + 2] cycloaddition between ketene and olefin linked with a 2,4-pentanediol (PD) tether. We find that the encounter of the ketene and olefin
P W Tas et al.
Biochimica et biophysica acta, 1026(1), 40-42 (1990-07-09)
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Eric J Bierschenk et al.
Inorganic chemistry, 50(23), 12126-12132 (2011-11-08)
When 2,4-pentanediol (2,4-H(2)pd) is deprotonated, the resulting dianion (2,4-pd) serves as a type of "hybrid" ligand, i.e., an alkoxide that possesses structural features of a β-diketonate. 2,4-Pentanediol reacts with Al(O-s-Bu)(3) and Zr(O-i-Pr)(4) to form chelated multinuclear complexes. The aluminum-containing product
Jun-Ichi Matsuo et al.
Organic letters, 12(10), 2294-2297 (2010-04-23)
Ketones and acyl silanes were reduced to the corresponding alcohols by a simple procedure employing anti-1,3-diol and a catalytic amount (5 mol %) of 2,4-dinitrobenzenesulfonic acid in benzene at reflux. Asymmetric induction reached up to >99% ee when a chiral
Belén Martín-Matute et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 12(23), 6053-6061 (2006-06-27)
Highly efficient synthesis of enantiopure diacetates of 2,4-pentanediol and 2,5-hexanediol starting from commercially available mixtures of the diols (dl/meso approximately 1:1) has been realized by combining a fast ruthenium-catalyzed epimerization with an enzymatic transesterification. The in situ coupling of these
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