ethyl 6-methylimidazo[1,2-a]pyridine-2-carboxylate
Modify Date: 2025-09-18 14:07:09
![ethyl 6-methylimidazo[1,2-a]pyridine-2-carboxylate Structure](https://image.chemsrc.com/caspic/019/70705-30-5.png)
ethyl 6-methylimidazo[1,2-a]pyridine-2-carboxylate structure
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Common Name | ethyl 6-methylimidazo[1,2-a]pyridine-2-carboxylate | ||
|---|---|---|---|---|
| CAS Number | 70705-30-5 | Molecular Weight | 285.137 | |
| Density | 1.19g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C11H13BrN2O2 | Melting Point | 50ºC (sub.) | |
| MSDS | N/A | Flash Point | N/A | |
| Name | ethyl 6-methylimidazo[1,2-a]pyridine-2-carboxylate |
|---|---|
| Synonym | More Synonyms |
| Density | 1.19g/cm3 |
|---|---|
| Melting Point | 50ºC (sub.) |
| Molecular Formula | C11H13BrN2O2 |
| Molecular Weight | 285.137 |
| Exact Mass | 284.016022 |
| PSA | 43.60000 |
| LogP | 1.81940 |
| Index of Refraction | 1.584 |
| Hazard Codes | Xi |
|---|---|
| HS Code | 2933990090 |
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ethyl 6-methyli... CAS#:70705-30-5 |
| Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 15, # 11 p. 2790 - 2794 |
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~30%
ethyl 6-methyli... CAS#:70705-30-5 |
| Literature: Rees, Charles W.; Smith, David I. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1987 , p. 1159 - 1164 |
![ethyl 6-methyl-3,5-dinitroimidazo[1,2-a]pyridine-2-carboxylate structure](https://image.chemsrc.com/caspic/293/72721-17-6.png)
![(6-methylimidazo[1,2-a]pyridin-2-yl)methanol structure](https://image.chemsrc.com/caspic/493/926223-25-8.png)
CAS#:926223-25-8| HS Code | 2933990090 |
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| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
| 6-methyl-imidazo[1,2-a]pyridine-2-carboxylic acid ethyl ester |
| 6-Methyl-imidazo<1,2-a>pyridin-2-carbonsaeureethylester |
| Imidazo[1,2-a]pyridine-2-carboxylic acid, 6-methyl-, ethyl ester, hydrobromide (1:1) |
| ethyl 6-methylimidazo<1,2-a>pyridine-2-carboxylate |
| Ethyl 6-methylimidazo[1,2-a]pyridine-2-carboxylate hydrobromide (1:1) |