Ethyl 4-bromobutyrate, 98%
Ethyl 4-bromobutyrate, 98%
Ethyl 4-bromobutyrate, 98%
Ethyl 4-bromobutyrate, 98%
Thermo Scientific Chemicals

Ethyl 4-bromobutyrate, 98%

CAS: 2969-81-5 | C6H11BrO2 | 195.056 g/mol
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Catalog number A13470.0B
also known as A13470-0B
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Quantity:
1000 g
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Price (EUR)
402,05
Online Exclusive
473,00
Save 70,95 (15%)
Each
Add to cart
Chemical Identifiers
CAS2969-81-5
IUPAC Nameethyl 4-bromobutanoate
Molecular FormulaC6H11BrO2
InChI KeyXBPOBCXHALHJFP-UHFFFAOYSA-N
SMILESCCOC(=O)CCCBr
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SpecificationsSpecification SheetSpecification Sheet
Identification (FTIR)Conforms
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥97.5%
Refractive Index1.4540-1.4580 @ 20?C
FormLiquid
Ethyl 4-bromobutyrate is used as a building block for the preparation of firefly luciferase inhibitor-conjucated peptide derivatives. It finds application in the synthesis of poly(2,6,-dimethyl-1,4-phehylene oxide) and thieno(2,3-b)-azepin-4-ones.

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 4-bromobutyrate is used as a building block for the preparation of firefly luciferase inhibitor-conjucated peptide derivatives. It finds application in the synthesis of poly(2,6,-dimethyl-1,4-phehylene oxide) and thieno(2,3-b)-azepin-4-ones.

Solubility
Immiscible with water.

Notes
Incompatible with bases, oxidizing agents and reducing agents.
RUO – Research Use Only

General References:

  1. Borzenkov, M.; Mitina, N.; Lobaz, V.; Hevus, O. Synthesis and Properties of Novel Surface Active Monomers Based on Derivatives of 4-Hydroxybutyric Acid and 6-Hydroxyhexanoic Acid. J. Surfactants Deterg. 2015, 18 (1), 133-144.
  2. Ali, S. A.; Muallem, H. A.; Hamouz, O. C. S. O. A.; Estaitie, M. K. Synthesis of a novel zwitterionic bisphosphonate cyclopolymer containing residues of alendronic acid. React. Funct. Polym. 2015, 86, 80-86.