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

Ethyl 4-chlorobutyrate, 98%, Thermo Scientific Chemicals

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100 g
500 g
Catalog number A11070.22
also known as A11070-22
Price (USD)/ Each
51.90
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Quantity:
100 g
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Price (USD)/ Each
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Ethyl 4-chlorobutyrate, 98%, Thermo Scientific Chemicals
Catalog numberA11070.22
Price (USD)/ Each
51.90
-
Add to cart
Chemical Identifiers
CAS3153-36-4
IUPAC Nameethyl 4-chlorobutanoate
Molecular FormulaC6H11ClO2
InChI KeyOPXNFHAILOHHFO-UHFFFAOYSA-N
SMILESCCOC(=O)CCCCl
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SpecificationsSpecification SheetSpecification Sheet
Identification (FTIR)Conforms
Refractive Index1.4295-1.4335 @ 20°C
FormLiquid
Appearance (Color)Clear colorless to yellow to brown
Assay (GC)≥97.5%
Ethyl 4-chlorobutyrate is used in organic synthesis. And also used for producting 4-Iodo-butyric acid ethyl ester.

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-chlorobutyrate is used in organic synthesis. And also used for producting 4-Iodo-butyric acid ethyl ester.

Solubility
Insoluble in water.

Notes
Hygroscopic. Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only

General References:

  1. Robert T. Buckler, Harold E. Hartzler, Elva Kurchacova, Gust Nichols, Barrie M. Phillips. Synthesis and antiinflammatory activity of some 1,2,3- and 1,2,4-triazolepropionic acids. J. Med. Chem. 1978, 21(12),1254-1260.
  2. G Chuchani,; RM Dominguez.The kinetics and mechanisms of the gas-phase pyrolysis of ethyl 4-bromobutyrate. The ion-pair mechanism revisited. International Journal of Chemical Kinetics. 1983, 15 (8), 795-803.