Search
元素の検索
構造の検索
Thermo Scientific Chemicals
Ethyl 4,6-dichloronicotinate, 95%, Thermo Scientific Chemicals
| 製品番号（カタログ番号） | 数量 |
|---|---|
| H63092.06 または、製品番号H63092-06 | 5 g |
化学物質識別子
CAS40296-46-6
IUPAC Nameethyl 4,6-dichloropyridine-3-carboxylate
Molecular FormulaC8H7Cl2NO2
InChI KeyAAUBVINEXCCXOK-UHFFFAOYSA-N
SMILESCCOC(=O)C1=CN=C(Cl)C=C1Cl
さらに表示
スペックシート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.
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:
- 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.
- 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.