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3-Cyclohexylpropionic acid, 98+%, Thermo Scientific Chemicals
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Catalog number B23613.30
also known as B23613-30
Price (USD)/ Each
250.00
-
Quantity:
250 g
Price (USD)/ Each
250.00
3-Cyclohexylpropionic acid, 98+%, Thermo Scientific Chemicals
Catalog numberB23613.30
Price (USD)/ Each
250.00
-
Chemical Identifiers
CAS701-97-3
IUPAC Name3-cyclohexylpropanoic acid
Molecular FormulaC9H16O2
InChI KeyHJZLEGIHUQOJBA-UHFFFAOYSA-N
SMILESOC(=O)CCC1CCCCC1
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Specifications
Specification Sheet
Specification SheetAssay (Aqueous acid-base Titration)≥98.0 to ≤102.0%
Refractive Index1.4620-1.4660 @ 20?C
Identification (FTIR)Conforms
Appearance (Color)Clear colorless to pale yellow
Assay (Silylated GC)≥98.0%
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3-Cyclohexylpropionic acid can be used to produce 3-cyclohexyl-propionyl chloride. It is used as pharmaceutical intermediates in organic synthesis. It can also be used for the synthesis of pineapple esters.
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-Cyclohexylpropionic acid can be used to produce 3-cyclohexyl-propionyl chloride. It is used as pharmaceutical intermediates in organic synthesis. It can also be used for the synthesis of pineapple esters.
Solubility
Soluble in water 10g/ L.
Notes
Store in cool, dry conditions in well sealed containers. Store away from oxidizing agents, bases.
3-Cyclohexylpropionic acid can be used to produce 3-cyclohexyl-propionyl chloride. It is used as pharmaceutical intermediates in organic synthesis. It can also be used for the synthesis of pineapple esters.
Solubility
Soluble in water 10g/ L.
Notes
Store in cool, dry conditions in well sealed containers. Store away from oxidizing agents, bases.
RUO – Research Use Only
General References:
- Leonard Spialter; Charles W. Harris. 2-Cyclohexylethyltricyclohexylsilan. Bildung von Cyclohexylethyllithium aus der Spaltung von Ethylether durch Cyclohexyllithium. J. Org. Chem. 1966, 31 (12), 4263-4264.
- M. Manning; W.A. Klis; M. Kruszynski; J.P. Przybylski; A. Olma; N.C. Wo; G.H. Pelton And W.H. Sawyer. Novel linear antagonists of the antidiuretic (V2) and vasopressor (V1) responses to vasopressin. International Journal of Peptide and Protein Research. 1988, 32 (6), 455-467.