Ethyl 5-bromovalerate, 98%, Thermo Scientific Chemicals
Ethyl 5-bromovalerate, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Ethyl 5-bromovalerate, 98%, Thermo Scientific Chemicals

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Quantity:
500 g
25 g
100 g
Catalog number A11952.36
also known as A11952-36
Price (USD)/ Each
832.00
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Quantity:
500 g
Request bulk or custom format
Price (USD)/ Each
832.00
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Ethyl 5-bromovalerate, 98%, Thermo Scientific Chemicals
Catalog numberA11952.36
Price (USD)/ Each
832.00
-
Add to cart
Chemical Identifiers
CAS14660-52-7
IUPAC Nameethyl 5-bromopentanoate
Molecular FormulaC7H13BrO2
InChI KeyAFRWBGJRWRHQOV-UHFFFAOYSA-N
SMILESCCOC(=O)CCCCBr
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥97.5%
FormLiquid
Refractive Index1.4570-1.4610 @ 20?C
Ethyl 5-bromovalerate is employed in the preparation of S(γ-Carboxypropyl)-DL-homocysteine and S(δ-Carboxybutyl)-DL-homocysteine. It is also used in the preparation of ethyl 5-azidovalerate.

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
Ethyl 5-bromovalerate is employed in the preparation of S(γ-Carboxypropyl)-DL-homocysteine and S(δ-Carboxybutyl)-DL-homocysteine. It is also used in the preparation of ethyl 5-azidovalerate.

Solubility
Not miscible or difficult to mix in water.

Notes
Light Sensitive. Keep away from oxidizing agents. Store in dark.
RUO – Research Use Only

General References:

  1. Zengmin Li.; Tae Seok Seo.; Jingyue Ju. 1,3-Dipolar cycloaddition of azides with electron-deficient alkynes under mild condition in water.Tetrahedron Lett.2004,45(15), 3143-3146.
  2. Fernando Albericio.; Nancy Kneib-Cordonier.; Sara Biancalana.; Lajos Gera.; R. Irene Masada.; Derek Hudson.; George Barany. Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions.J. Org. Chem.,1990,55(12), 3730-3743.