Terephthalaldehyde mono(diethyl acetal), 97%, stab.
Terephthalaldehyde mono(diethyl acetal), 97%, stab.
Terephthalaldehyde mono(diethyl acetal), 97%, stab.
Terephthalaldehyde mono(diethyl acetal), 97%, stab.
Thermo Scientific Chemicals

Terephthalaldehyde mono(diethyl acetal), 97%, stab.

CAS: 81172-89-6 | C12H16O3 | 208.26 g/mol
数量:
5 g
25 g
100 g
製品番号(カタログ番号) A15413.06
または、製品番号A15413-06
価格(JPY)
-
見積もりを依頼する
数量:
5 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS81172-89-6
Appearance (Color)Clear colorless to yellow
Assay (GC)≥96.0%
Refractive Index1.5050-1.5090 @ 20?C
FormLiquid
Stabilizer0.1% triethylamine
4-(Diethoxymethyl)benzaldehyde was used in the synthesis of 4-(diethoxymethyl)benzyl alcohol.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4-(Diethoxymethyl)benzaldehyde was used in the synthesis of 4-(diethoxymethyl)benzyl alcohol.

Solubility
soluble in alcohol, chlorinated solvents and toluene. Decomposes in water.

Notes
Air sensitive. Store under inert gas. Keep way from oxidizing agents, air.
RUO – Research Use Only

General References:

  1. Yoshitsugu Akiyama; Yukio Nagasaki; Kazunori Kataoka. Synthesis of heterotelechelic poly(ethylene glycol) derivatives having alpha-benzaldehyde and μ-pyridyl disulfide groups by ring opening polymerization of ethylene oxide using 4-(diethoxymethyl)benzyl alkoxide as a novel initiator. Bioconjugate Chemistry. 2004, 15, (2), 424-427.
  2. Kyle J. Eash; Michael S. Pulia; Laura C. Wieland and Ram S. Mohan. A Simple Chemoselective Method for the Deprotection of Acetals and Ketals Using Bismuth Nitrate Pentahydrate. J. Org. Chem. 2000, 65(24), 8399-8401.