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Merck
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156019

Sigma-Aldrich

2,4-戊二醇

98%

同義詞:

1,3-二甲基丙烷-1,3-二醇, 2,4-二羟基戊烷, 2,4-戊二醇

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About This Item

線性公式:
CH3CH(OH)CH2CH(OH)CH3
CAS號碼:
分子量::
104.15
Beilstein:
969186
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

liquid

折射率

n20/D 1.435 (lit.)

bp

201-202 °C (lit.)

密度

0.95 g/mL at 25 °C (lit.)

SMILES 字串

CC(O)CC(C)O

InChI

1S/C5H12O2/c1-4(6)3-5(2)7/h4-7H,3H2,1-2H3

InChI 密鑰

GTCCGKPBSJZVRZ-UHFFFAOYSA-N

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應用

2,4-戊二醇用于合成螯合的多核络合物

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

213.8 °F - closed cup

閃點(°C)

101.00 °C - closed cup

個人防護裝備

Eyeshields, Gloves


分析證明 (COA)

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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)
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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