4-tert-Butylthiophenol, 97%
4-tert-Butylthiophenol, 97%
4-tert-Butylthiophenol, 97%
4-tert-Butylthiophenol, 97%
Thermo Scientific Chemicals

4-tert-Butylthiophenol, 97%

CAS: 2396-68-1 | C10H14S | 166.282 g/mol
製品番号(カタログ番号) A12148.14
または、製品番号A12148-14
価格(JPY)
-
見積もりを依頼する
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
CAS2396-68-1
IUPAC Name4-tert-butylbenzene-1-thiol
Molecular FormulaC10H14S
InChI KeyGNXBFFHXJDZGEK-UHFFFAOYSA-N
SMILESCC(C)(C)C1=CC=C(S)C=C1
さらに表示
Assay (GC)≥96.0%
Refractive Index1.5455-1.5505 @ 20?C
Appearance (Color)Clear colorless to pale yellow
FormLiquid
Identification (FTIR)Conforms
4-tert-butylthiophenol is used as a 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
4-tert-butylthiophenol is used as a pharmaceutical intermediate.

Solubility
Insoluble in water.

Notes
Air sensitive. Store under inert gas. Store away from oxidizing agents.
RUO – Research Use Only

General References:

  1. Feng Wang & Masahiro Tada. Asymmetric Michael Addition with Amino Alcohol Catalysts Derived from d-Glucose. Agricultural and Biological Chemistry. 1990, 54 (11), 370-375.
  2. Paul McDaid; Yonggang Chen and Li Deng Dr. A Highly Enantioselective and General Conjugate Addition of Thiols to Cyclic Enones with an Organic Catalyst. ACS Catalysis. 2002, 114 (2), 348-350.