5-BROMO-2-METHYL-NICOTINIC ACID ETHYL ESTER
5-BROMO-2-METHYL-NICOTINIC ACID ETHYL ESTER Basic information
- Product Name:
- 5-BROMO-2-METHYL-NICOTINIC ACID ETHYL ESTER
- Synonyms:
-
- 5-BROMO-2-METHYL-NICOTINIC ACID ETHYL ESTER
- 5-Bromo-2-methylnicotinic acid ethyl ester ,98%
- 5-BroMo-2-Methylnicotinic acid ethyl esther
- ethyl 5-broMo-2-Methylpyridine-3-carboxylate
- 3-Pyridinecarboxylic acid, 5-broMo-2-Methyl-, ethyl ester
- Ethyl 5-broMo-2-Methylnicotinate
- 5-Bromo-2-methyl-3-pyridinecarboxylic acid ethyl ester
- 5-BroMo-2-Methylnicotini
- CAS:
- 129477-21-0
- MF:
- C9H10BrNO2
- MW:
- 244.09
- Mol File:
- 129477-21-0.mol
5-BROMO-2-METHYL-NICOTINIC ACID ETHYL ESTER Chemical Properties
- Boiling point:
- 263℃
- Density
- 1.439
- Flash point:
- 113℃
- storage temp.
- Inert atmosphere,Room Temperature
- form
- Solid
- pka
- 1.66±0.20(Predicted)
- color
- Pale yellow
- Water Solubility
- Slightly soluble in water.
- InChI
- InChI=1S/C9H10BrNO2/c1-3-13-9(12)8-4-7(10)5-11-6(8)2/h4-5H,3H2,1-2H3
- InChIKey
- QVKPPFGWQMCQCI-UHFFFAOYSA-N
- SMILES
- C1(C)=NC=C(Br)C=C1C(OCC)=O
- CAS DataBase Reference
- 129477-21-0
Safety Information
- Safety Statements
- 24/25
- HS Code
- 29333990
5-BROMO-2-METHYL-NICOTINIC ACID ETHYL ESTER Usage And Synthesis
Uses
Ethyl 5-bromo-2-methylnicotinate is used as a pharmaceutical intermediate.
Synthesis
To a 250 mL triple-necked flask were added sequentially 4. 9 g of methyl 5-bromo-2-methylnicotinate ( 0. 04 mol), anhydrous ethanol 40 mL, the corresponding amount of concentrated sulfuric acid, and phase transfer catalyst; a stirrer and a distillation apparatus were installed separately. Heat with stirring, gradually increase the temperature, evaporate the ethanol to the required liquid temperature, stop heating, natural cooling, about . 50?? C. It is poured out, and the reactants are white solids at room temperature. Neutralize the product with saturated aqueous sodium carbonate to a pH of about 7 (some solid sodium carbonate may be added if the volume is too large) and extract with 20 of chloroform. mL of chloroform, the combined organic layers were transferred to a reduced-pressure distillation flask, the chloroform was recovered at atmospheric pressure and then ethyl 5-bromo-2-methylnicotinate was distilled at reduced pressure, and the 92- to fraction was collected at 1. 06 kPa. The fraction was collected at 1.06 kPa from 92 to , weighed and the yield was calculated.
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5-BROMO-2-METHYL-NICOTINIC ACID ETHYL ESTER(129477-21-0)Related Product Information
- N-Methylpropionamide
- 5-METHYLCYTOSINE
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- 5-BROMO-2-METHYLNICOTINIC ACID
- Nicotinic acid
- ETHYL STEARATE
- 5-bromo-2-pyridinecarboxylic acid ethyl ester
- Ethyl 2-chloronicotinate
- ETHYL 2-METHYL-5-NITRONICOTINATE
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