IMidazo[1,2-a]pyridine, 8-Methoxy
IMidazo[1,2-a]pyridine, 8-Methoxy-
CAS: 100592-04-9
Molecular Formula: C8H8N2O
IMidazo[1,2-a]pyridine, 8-Methoxy - Names and Identifiers
| Name | IMidazo[1,2-a]pyridine, 8-Methoxy- |
| Synonyms | 8-Methoxy-iMidazo[1,2-a]pyridine IMidazo[1,2-a]pyridine, 8-Methoxy IMidazo[1,2-a]pyridine, 8-Methoxy- |
| CAS | 100592-04-9 |
IMidazo[1,2-a]pyridine, 8-Methoxy - Physico-chemical Properties
| Molecular Formula | C8H8N2O |
| Molar Mass | 148.16 |
| Density | 1.18±0.1 g/cm3(Predicted) |
| pKa | 5.89±0.50(Predicted) |
| Storage Condition | 2-8°C |
IMidazo[1,2-a]pyridine, 8-Methoxy - Introduction
8-Methoxy-imidazo [1,2-a] pyridine is an organic compound with the chemical formula C9H9N2O. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: 8-Methoxy-imidazo [1,2-a] pyridine as a white to light yellow crystalline solid.
-Molecular weight: 163.19g/mol.
-Melting point: approximately 136-137°C.
-Solubility: Soluble in common organic solvents (such as ethanol, chloroform and dimethyl sulfoxide), but less soluble in water.
-Stability: It is stable and not easy to decompose under conventional storage conditions.
Use:
-8-methoxy-imidazo [1,2-a] pyridine can be used as an organic synthesis intermediate for the synthesis of other compounds.
-The compound also has certain applications in the field of medicine, such as the synthesis of biologically active compounds.
Preparation Method:
-8-Methoxy-imidazo [1,2-a] pyridine can be prepared by a variety of synthetic routes. One commonly used method is the reaction of methylimidazo [1,2-a] pyridine with methanol to give the product.
Safety Information:
Nature:
-Appearance: 8-Methoxy-imidazo [1,2-a] pyridine as a white to light yellow crystalline solid.
-Molecular weight: 163.19g/mol.
-Melting point: approximately 136-137°C.
-Solubility: Soluble in common organic solvents (such as ethanol, chloroform and dimethyl sulfoxide), but less soluble in water.
-Stability: It is stable and not easy to decompose under conventional storage conditions.
Use:
-8-methoxy-imidazo [1,2-a] pyridine can be used as an organic synthesis intermediate for the synthesis of other compounds.
-The compound also has certain applications in the field of medicine, such as the synthesis of biologically active compounds.
Preparation Method:
-8-Methoxy-imidazo [1,2-a] pyridine can be prepared by a variety of synthetic routes. One commonly used method is the reaction of methylimidazo [1,2-a] pyridine with methanol to give the product.
Safety Information:
Last Update：2024-04-09 02:00:40
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View History
IMidazo[1,2-a]pyridine, 8-Methoxy
3'-Guanylic acid, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-P-(4-chlorophenyl)thymidylyl-(3'->5')-2'-deoxy-N-(2-methyl-1-oxopropyl)-, 4-chlorophenyl 2-cyanoethyl ester
SMP-Na
GMMMFXKCRYRKEZ-UHFFFAOYSA-N
PHENYL-D5-BORONIC ACID
NEP1-40; NOGO EXTRACELLULAR PEPTIDE; 1-40
1-CETYLPYRIDINIUM CHLORIDE 1-HYDRATE
Dimethylaminomethyl ferrocene
Hydrazinecarbothioamide, 2-propylidene-
2-巯基-6-甲基-5-丙基嘧啶-4-醇
3'-Guanylic acid, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-P-(4-chlorophenyl)thymidylyl-(3'->5')-2'-deoxy-N-(2-methyl-1-oxopropyl)-, 4-chlorophenyl 2-cyanoethyl ester
SMP-Na
GMMMFXKCRYRKEZ-UHFFFAOYSA-N
PHENYL-D5-BORONIC ACID
NEP1-40; NOGO EXTRACELLULAR PEPTIDE; 1-40
1-CETYLPYRIDINIUM CHLORIDE 1-HYDRATE
Dimethylaminomethyl ferrocene
Hydrazinecarbothioamide, 2-propylidene-
2-巯基-6-甲基-5-丙基嘧啶-4-醇