Ethyl 4,6-dichloronicotinate, 95%, Thermo Scientific Chemicals
Ethyl 4,6-dichloronicotinate, 95%, Thermo Scientific Chemicals
Ethyl 4,6-dichloronicotinate, 95%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Ethyl 4,6-dichloronicotinate, 95%, Thermo Scientific Chemicals

Catalog NumberQuantity
H63092.06
also known as H63092-06
5 g
Catalog number H63092.06
also known as H63092-06
Price (JPY)
-
Quantity:
5 g
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Chemical Identifiers
CAS40296-46-6
IUPAC Nameethyl 4,6-dichloropyridine-3-carboxylate
Molecular FormulaC8H7Cl2NO2
InChI KeyAAUBVINEXCCXOK-UHFFFAOYSA-N
SMILESCCOC(=O)C1=CN=C(Cl)C=C1Cl
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to off-white
Assay (HPLC)≥94.0%
FormLow-melting solid
Ethyl 4,6-dichloronicotinate, is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is also used as a fine chemical intermediate.

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 4,6-dichloronicotinate, is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is also used as a fine chemical intermediate.

Solubility
Soluble in methanol.

Notes
Heat sensitive. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Keep away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. H Sun.; SG DiMagno. Fluoride relay: a new concept for the rapid preparation of anhydrous nucleophilic fluoride salts from KF. Chem. Commun.20078 (5), 528-529.
  2. R Baharfar.; R Azimi. Immobilization of 1,4-Diazabicyclo[2.2.2]Octane (DABCO) over Mesoporous Silica SBA-15: An Efficient Approach for the Synthesis of Functionalized Spirochromenes. Synthetic Communications.201444 (1), 89-100.