2-n-Butylthiophene, 98+%
2-n-Butylthiophene, 98+%
2-n-Butylthiophene, 98+%
Thermo Scientific Chemicals

2-n-Butylthiophene, 98+%

CAS: 1455-20-5 | C8H12S | 140.244 g/mol
Quantity:
5 g
25 g
Catalog number A12740.06
also known as A12740-06
Price (JPY)
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Quantity:
5 g
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Chemical Identifiers
CAS1455-20-5
IUPAC Name2-butylthiophene
Molecular FormulaC8H12S
InChI KeyMNDZHERKKXUTOE-UHFFFAOYSA-N
SMILESCCCCC1=CC=CS1
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SpecificationsSpecification SheetSpecification Sheet
Refractive Index1.4995-1.5035 @ 20°C
Appearance (Color)Clear colorless to yellow to brown
FormLiquid
Assay (GC)≥98.0%
2-n-Butylthiophene is an inhibitor of DMH-induced aberrant crypt formation. It is used as a Glutathione S-transferase inducer. It is used as a primary and secondary 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
2-n-Butylthiophene is an inhibitor of DMH-induced aberrant crypt formation. It is used as a Glutathione S-transferase inducer. It is used as a primary and secondary intermediate.

Solubility
Soluble in acetone and DMSO.

Notes
Storage temperature: 2 - 4°Cand Keep container tightlyclosed in a dryand well-ventilated place. Incompatible to Strong oxidizing agents.
RUO – Research Use Only

General References:

  1. LKT Lam.; BL Zheng. Inhibitory effects of 2-n-heptylfuran and 2-n-butylthiophene on benzo [a] pyrene-induced lung and forestomach tumorigenesis in A/J mice. Nutrition and Cancer. 1992 17, (1) , 19-26.
  2. J Roger.; F Požgan.; H Doucet. Ligand-less palladium-catalyzed direct 5-arylation of thiophenes at low catalyst loadings. Green Chemistry. 2009 11, (3) , 425-432.