3-Furaldehyde structure
|
Common Name | 3-Furaldehyde | ||
|---|---|---|---|---|
| CAS Number | 498-60-2 | Molecular Weight | 96.084 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 145.3±0.0 °C at 760 mmHg | |
| Molecular Formula | C5H4O2 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 48.3±0.0 °C | |
| Symbol |
GHS02, GHS07 |
Signal Word | Warning | |
Use of 3-Furaldehyde3-Furaldehyde is a member of furans and an aldehyde, and can be used to synthesize the neoclerodane diterpene Salvinorin A[1][2]. |
| Name | 3-furaldehyde |
|---|---|
| Synonym | More Synonyms |
| Description | 3-Furaldehyde is a member of furans and an aldehyde, and can be used to synthesize the neoclerodane diterpene Salvinorin A[1][2]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 145.3±0.0 °C at 760 mmHg |
| Molecular Formula | C5H4O2 |
| Molecular Weight | 96.084 |
| Flash Point | 48.3±0.0 °C |
| Exact Mass | 96.021126 |
| PSA | 30.21000 |
| LogP | 0.51 |
| Vapour Pressure | 4.9±0.2 mmHg at 25°C |
| Index of Refraction | 1.515 |
| InChIKey | AZVSIHIBYRHSLB-UHFFFAOYSA-N |
| SMILES | O=Cc1ccoc1 |
| Storage condition | 2-8°C |
| Symbol |
GHS02, GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H226-H315-H319-H335 |
| Precautionary Statements | P261-P305 + P351 + P338 |
| Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
| Hazard Codes | Xi:Irritant; |
| Risk Phrases | R10;R36/37/38 |
| Safety Phrases | S26-S36-S45-S36/37-S16 |
| RIDADR | UN 1989 3/PG 3 |
| WGK Germany | 3 |
| Packaging Group | III |
| Hazard Class | 3 |
| HS Code | 2932190090 |
| Precursor 9 | |
|---|---|
| DownStream 10 | |
| HS Code | 2932190090 |
|---|---|
| Summary | 2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0% |
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Paternò-Büchi reaction between furan and heterocyclic aldehydes: oxetane formation vs. metathesis.
Photochem. Photobiol. Sci. 9(8) , 1134-8, (2010) The photochemical reaction of 2-substituted heterocyclic aldehydes with furan gave the corresponding exo oxetane derivatives through the excited triplet state. However, in situ the oxetane derivatives... |
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Name: Inhibition of xanthine oxidase at IC50 concentration
Source: ChEMBL
Target: N/A
External Id: CHEMBL3051424
|
|
Name: Inhibition of Oryctolagus cuniculus (rabbit) AOX in liver cytosol
Source: ChEMBL
Target: Aldehyde oxidase 1
External Id: CHEMBL3051430
|
|
Name: Inhibition of Agaricus bisporus (mushroom) tyrosinase
Source: ChEMBL
Target: Polyphenol oxidase 2
External Id: CHEMBL3051431
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| MFCD00010424 |
| 3-Furaldehyde |
| 3-Furancarboxaldehyde |
| furan-3-carbaldehyde |