1,3-Propanediol di-p-toluenesulfonate, 98%, Thermo Scientific Chemicals
1,3-Propanediol di-p-toluenesulfonate, 98%, Thermo Scientific Chemicals
1,3-Propanediol di-p-toluenesulfonate, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

1,3-Propanediol di-p-toluenesulfonate, 98%, Thermo Scientific Chemicals

製品番号(カタログ番号)数量
B21084.14
または、製品番号B21084-14
25 g
製品番号(カタログ番号) B21084.14
または、製品番号B21084-14
価格(JPY)
-
数量:
25 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
CAS5469-66-9
IUPAC Name3-[(4-methylbenzenesulfonyl)oxy]propyl 4-methylbenzene-1-sulfonate
Molecular FormulaC17H20O6S2
InChI KeyODVREDGIWSDQFD-UHFFFAOYSA-N
SMILESCC1=CC=C(C=C1)S(=O)(=O)OCCCOS(=O)(=O)C1=CC=C(C)C=C1
さらに表示
Appearance (Color)White
FormPowder
Assay (HPLC)≥97.5%
Melting Point (clear melt)90.0-96.0?C
Used as pharmaceutical intermediate.

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
Used as pharmaceutical intermediate.

Notes
Store at room temperature. Keep away from oxidizing agents.
RUO – Research Use Only

General References:

  1. William H. Pearson.; Patrick Stoy.; Yuan Mi. A Three-Component, One-Pot Synthesis of Indolizidines and Related Heterocycles via the [3+2] Cycloaddition of Nonstabilized Azomethine Ylides. J. Org. Chem. 2004, 69 (6),1919-1939 .
  2. Phillip T. Berkowitz.; Kurt Baum. Reactions of 2-fluoro-2-nitro-1,3-propanediol. p-Toluenesulfonates. J. Org. Chem. 1981, 46 (19),3816-3819 .