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4-Benzyl-4-hydroxypiperidine, 97%, Thermo Scientific Chemicals
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Catalog number A15664.03
also known as A15664-03
Price (USD)/ Each
64.10
-
Quantity:
1 g
Price (USD)/ Each
64.10
4-Benzyl-4-hydroxypiperidine, 97%, Thermo Scientific Chemicals
Catalog numberA15664.03
Price (USD)/ Each
64.10
-
Chemical Identifiers
CAS51135-96-7
IUPAC Name4-benzyl-4-hydroxypiperidin-1-ium
Molecular FormulaC12H18NO
InChI KeyKJZBZOFESQSBCV-UHFFFAOYSA-O
SMILESOC1(CC2=CC=CC=C2)CC[NH2+]CC1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream
Assay (GC)≥96.0%
FormCrystals or powder or crystalline powder
Water Content (Karl Fischer Titration)≤2.5%
It is a building block used for the synthesis of various compounds, having therapeutic properties, such as synthesis of 4-Benzimidazolyl-piperidinylcarbonyl-piperidine analogs as histamine H3 antagonists.
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
It is a building block used for the synthesis of various compounds, having therapeutic properties, such as synthesis of 4-Benzimidazolyl-piperidinylcarbonyl-piperidine analogs as histamine H3 antagonists.
Solubility
Slightly soluble in water.
Notes
Hygroscopic. Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
It is a building block used for the synthesis of various compounds, having therapeutic properties, such as synthesis of 4-Benzimidazolyl-piperidinylcarbonyl-piperidine analogs as histamine H3 antagonists.
Solubility
Slightly soluble in water.
Notes
Hygroscopic. Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only
General References:
- Laura C. Cooper, et al. 2-Aryl Indole NK1 receptor antagonists: optimisation of indole substitution.Bioorg. Med. Chem. Lett.,2009,11(9), 1233-1236.
- Duncan Shawa, et al. 2-Aryl indole NK1 antagonists: optimisation of the amide substituent.Bioorg. Med. Chem. Lett.,2001,11(23), 3031-3034.