추천 제품
분석
98%
양식
liquid
refractive index
n20/D 1.435 (lit.)
bp
201-202 °C (lit.)
density
0.95 g/mL at 25 °C (lit.)
작용기
hydroxyl
SMILES string
CC(O)CC(C)O
InChI
1S/C5H12O2/c1-4(6)3-5(2)7/h4-7H,3H2,1-2H3
InChI key
GTCCGKPBSJZVRZ-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
2,4-Pentanediol was used in the synthesis of chelated multinuclear complexes.
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point (°F)
213.8 °F - closed cup
Flash Point (°C)
101.00 °C - closed cup
개인 보호 장비
Eyeshields, Gloves
이미 열람한 고객
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)
Lack of selectivity towards anesthetic stereoisomers is one of the few criteria available for the identification of an anesthetic target site. Until now this criterion has not been tested for anesthetics that directly interact with sensitive membrane proteins which are
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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