2,1,3-benzoxadiazole-4-carbaldehyde - Names and Identifiers
Name | 4-Benzofurazancarboxaldehyde
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Synonyms | 4-Benzofurazancarboxaldehyde 4-Formyl-2,1,3-benzoxadiazole 2,1,3-Benzoxadiazole-4-aldehyde 2,1,3-benzoxadiazole-4-carbaldehyde 2,1,3-Benzoxadiazole-4-carboxaldehyde Benzo[c][1,2,5]oxadiazole-4-carbaldehyde
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CAS | 32863-32-4
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EINECS | 682-565-9 |
InChI | InChI=1/C7H4N2O2/c10-4-5-2-1-3-6-7(5)9-11-8-6/h1-4H |
2,1,3-benzoxadiazole-4-carbaldehyde - Physico-chemical Properties
Molecular Formula | C7H4N2O2
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Molar Mass | 148.12 |
Density | 1.418g/cm3 |
Melting Point | 100-102°C |
Boling Point | 277.254°C at 760 mmHg |
Flash Point | 121.479°C |
Vapor Presure | 0.005mmHg at 25°C |
Appearance | Solid |
pKa | -1.86±0.45(Predicted) |
Storage Condition | Inert atmosphere,2-8°C |
Refractive Index | 1.677 |
MDL | MFCD07772900 |
2,1,3-benzoxadiazole-4-carbaldehyde - Risk and Safety
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin.
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Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
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Hazard Class | IRRITANT |
2,1,3-benzoxadiazole-4-carbaldehyde - Upstream Downstream Industry
2,1,3-benzoxadiazole-4-carbaldehyde - Introduction
The chemical formula is C8H5N3O2, which is an organic compound. Its properties are as follows:
1. Appearance: White to light yellow solid.
2. Solubility: soluble in organic solvents such as alcohol, ether and ketone, insoluble in water.
The main uses of calcium include the following:
1. Chemical reagents: as an important intermediate for the synthesis of other compounds.
2. Luminescent materials: with fluorescent properties, can be used for research and application in the field of optoelectronic devices.
3. Biomarkers: can be used as the detection and labeling of certain biological molecules.
There are several main methods of preparation:
1. Redox reaction: React an appropriate amount of benzoxadiazole with chloric acid under acidic conditions, and then use sodium nitrite to reduce the resulting benzoxadiazole derivative to fluorite.
2. Reaction coupling method: through the reaction of benzyl sodium sulfate and sodium cyanide, benzoxadiazole-4-sodium sulfate is generated, and then it is reacted with hydrochloric acid to obtain benzoxadiazole-4-sodium sulfate.
However, please note the following safety information:
1. The eye and skin irritation, contact should pay attention to the use of personal protective equipment.
2. May cause allergic reactions, it can not be excessive exposure to the smell or dust.
3. It should be used in a well-ventilated place and avoid inhalation or intake.
4. Should be properly stored, away from fire, heat and oxidant.
5. Please comply with the relevant safety procedures and guidelines.
Last Update:2024-04-10 22:41:03