3,4-Di-n-butoxy-3-cyclobutene-1,2-dione, 97%
3,4-Di-n-butoxy-3-cyclobutene-1,2-dione, 97%
3,4-Di-n-butoxy-3-cyclobutene-1,2-dione, 97%
3,4-Di-n-butoxy-3-cyclobutene-1,2-dione, 97%
Thermo Scientific Chemicals

3,4-Di-n-butoxy-3-cyclobutene-1,2-dione, 97%

CAS: 2892-62-8 | C12H18O4 | 226.27 g/mol
製品番号(カタログ番号) A18960.06
または、製品番号A18960-06
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
CAS2892-62-8
IUPAC Namedibutoxycyclobut-3-ene-1,2-dione
Molecular FormulaC12H18O4
InChI KeyXBRWELTXMQSEIN-UHFFFAOYSA-N
SMILESCCCCOC1=C(OCCCC)C(=O)C1=O
さらに表示
Appearance (Color)Clear colorless to yellow
FormLiquid
Assay (GC)≥96.0%
Identification (FTIR)Conforms
Refractive Index1.4930-1.4970 @ 20°C
3,4-Dibutoxy-3-cyclobutene-1,2-dione was used in the synthesis of novel semisquarylium dye, useful for highly selective Hg2+ sensing in aqueous media. It was also employed in the synthesis of 3-butoxy-4-(1,3,3-trimethyl-2,3-dihydro-1H-2-indolylidenemethyl)-3-cyclobutene-1,2-dione, intermediate for the synthesis of squaryl dyes.

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
3,4-Dibutoxy-3-cyclobutene-1,2-dione was used in the synthesis of novel semisquarylium dye, useful for highly selective Hg2+ sensing in aqueous media. It was also employed in the synthesis of 3-butoxy-4-(1,3,3-trimethyl-2,3-dihydro-1H-2-indolylidenemethyl)-3-cyclobutene-1,2-dione, intermediate for the synthesis of squaryl dyes.

Solubility
Insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Bae J-S, et al. A benzothiazole-based semisquarylium dye suitable for highly selective Hg2+ sensing in aqueous media.. Dyes and Pigments. 2009, 83(3), 324-27.
  2. Shishkina SV, et al. Molecular and crystal structure of 3-butoxy-4-(1, 3, 3-trimethyl-2, 3-dihydro-1H-2-indolylidenemethyl)-3-cyclobutene-1, 2-dione and its thio analog. J. Struct. Chem. 2005, 46 (1), 154-58.
  3. Reaction with alkyl- or aryllithium compounds results in ring opening to give the corresponding symmetrical 2,3-dibutoxy-1,4-diketones in high yield: Tetrahedron., 51, 12373 (1995).