162364-72-9
7-Benzyloxy-4-chloro-6-methoxyquinazoline
CAS: 162364-72-9
Molecular Formula: C16H13ClN2O2
162364-72-9 - Names and Identifiers
| Name | 7-Benzyloxy-4-chloro-6-methoxyquinazoline |
| Synonyms | 7-Benzyloxy-4-chloro-6-methoxy-quizoline 4-chloro-7-benzyloxy-6-methoxyquinazoline 4-Chloro-6-methoxy-7-benzyloxyquinazoline 7-Benzyloxy-4-chloro-6-methoxyquinazoline 4-chloro-7-benzyloxy -6-Methoxyquinazoline 7-BENZYLOXY-4-CHLORO-6-METHOXY-QUINAZOLINE 7-(benzyloxy)-4-chloro-6-methoxyquinazoline 4-chloro-6-methoxy-7-(phenylmethoxy)quinazoline Quinazoline, 4-chloro-6-Methoxy-7-(phenylMethoxy)- |
| CAS | 162364-72-9 |
| EINECS | 810-462-2 |
| InChI | InChI=1/C16H13ClN2O2/c1-20-14-7-12-13(18-10-19-16(12)17)8-15(14)21-9-11-5-3-2-4-6-11/h2-8,10H,9H2,1H3 |
162364-72-9 - Physico-chemical Properties
| Molecular Formula | C16H13ClN2O2 |
| Molar Mass | 300.74 |
| Density | 1.303±0.06 g/cm3(Predicted) |
| Boling Point | 452.1±40.0 °C(Predicted) |
| Flash Point | 227.198°C |
| Vapor Presure | 0mmHg at 25°C |
| pKa | 0.72±0.30(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
| Refractive Index | 1.639 |
162364-72-9 - Introduction
Boc benzyloxyquinazoline, also known as Boc benzyloxyquinazoline, is an organic compound. Its chemical formula is C13H12ClNO2.
In terms of nature, it is a white to pale yellow crystal with a taste of nicotinic acid ester. It is stable at room temperature, but may decompose under high temperature or strong light. It is soluble in solvents.
The main use of this compound is as a reagent in organic synthesis. It can be used to synthesize a variety of bioactive compounds, such as drugs, pesticides and biomarkers. It can also be used as a catalyst and as a ligand for transition metal complexes.
in terms of preparation method, P-chlorobenzoic acid methyl ester can be obtained by reacting p-methoxybenzoic acid with phosphorus chloride pentachloride, and then reacted with 2-aminopyridine to generate 4-chloro-6-methoxyquinazoline, finally, the target product was obtained by oxidation with benzyl ammonium bromide.
When using this compound, you need to pay attention to safety matters. It may be irritating to the skin, eyes and respiratory system and direct contact should be avoided. Wear appropriate protective gloves and glasses and operate in a well-ventilated area. If exposed or inhaled, wash the affected area immediately and seek medical help. In addition, the compound should be stored and handled properly to avoid incompatibility with other chemicals.
In terms of nature, it is a white to pale yellow crystal with a taste of nicotinic acid ester. It is stable at room temperature, but may decompose under high temperature or strong light. It is soluble in solvents.
The main use of this compound is as a reagent in organic synthesis. It can be used to synthesize a variety of bioactive compounds, such as drugs, pesticides and biomarkers. It can also be used as a catalyst and as a ligand for transition metal complexes.
in terms of preparation method, P-chlorobenzoic acid methyl ester can be obtained by reacting p-methoxybenzoic acid with phosphorus chloride pentachloride, and then reacted with 2-aminopyridine to generate 4-chloro-6-methoxyquinazoline, finally, the target product was obtained by oxidation with benzyl ammonium bromide.
When using this compound, you need to pay attention to safety matters. It may be irritating to the skin, eyes and respiratory system and direct contact should be avoided. Wear appropriate protective gloves and glasses and operate in a well-ventilated area. If exposed or inhaled, wash the affected area immediately and seek medical help. In addition, the compound should be stored and handled properly to avoid incompatibility with other chemicals.
Last Update：2024-04-10 22:30:50
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