5-Fluoro-2-hydroxybenzaldehyde structure
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Common Name | 5-Fluoro-2-hydroxybenzaldehyde | ||
|---|---|---|---|---|
| CAS Number | 347-54-6 | Molecular Weight | 140.11 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 207.4±20.0 °C at 760 mmHg | |
| Molecular Formula | C7H5FO2 | Melting Point | 82-85 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 79.2±21.8 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of 5-Fluoro-2-hydroxybenzaldehyde5-Fluoro-2-hydroxybenzaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| Name | 5-fluoro-2-hydroxybenzaldehyde |
|---|---|
| Synonym | More Synonyms |
| Description | 5-Fluoro-2-hydroxybenzaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
|---|---|
| Related Catalog |
| Density | 1.4±0.1 g/cm3 |
|---|---|
| Boiling Point | 207.4±20.0 °C at 760 mmHg |
| Melting Point | 82-85 °C(lit.) |
| Molecular Formula | C7H5FO2 |
| Molecular Weight | 140.11 |
| Flash Point | 79.2±21.8 °C |
| Exact Mass | 140.027359 |
| PSA | 37.30000 |
| LogP | 2.10 |
| Vapour Pressure | 0.2±0.4 mmHg at 25°C |
| Index of Refraction | 1.587 |
| InChIKey | FDUBQNUDZOGOFE-UHFFFAOYSA-N |
| SMILES | O=Cc1cc(F)ccc1O |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H315-H319-H335 |
| Precautionary Statements | P261-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xi:Irritant; |
| Risk Phrases | R36/37/38 |
| Safety Phrases | S26-S36 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2913000090 |
| Precursor 10 | |
|---|---|
| DownStream 10 | |
| HS Code | 2913000090 |
|---|---|
| Summary | HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0% |
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Large perturbations of long-range n J (1H, 1H) and n J (1H, 19F) by the intramolecular hydrogen bonds in 2-mercaptobenzaldehyde, salicylaldehyde, and some derivatives. Reference structures for intramolecular hydrogen bonds. Schaefer T, et al.
Can. J. Chem. 71(7) , 960-967, (1993)
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Manganese (III) complexes derived from bis-Schiff bases: Synthesis, structures, and antimicrobial activity. Liu QR, et al.
Russ. J. Coord. Chem. 40(10) , 757-763, (2014)
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Synthesis of Enantiopure 4-Amino-6-fluoro-3-(hydroxymethyl) chromanes via Intramolecular Nitrone Cycloadditions. Broggini G, et al.
J. Chem. Res. Synop. 2 , 36-37, (1997)
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| VHR BQ EF |
| 5-fluoro-2-hydroxy-benzaldehyde |
| 2-hydroxy-5-fluorobenzaldehyde |
| MFCD01090997 |
| 5-Fluoro-2-hydroxybenzaldehyde |
| 5-Fluorosalicylaldehyde |
| 4-fluoro-2-formylphenol |
| 5-fluorosalicyclaldehyde |