Methyl 4-formylbenzoate structure 
             | 
        Common Name | Methyl 4-formylbenzoate | ||
|---|---|---|---|---|
| CAS Number | 1571-08-0 | Molecular Weight | 164.158 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 265.0±0.0 °C at 760 mmHg | |
| Molecular Formula | C9H8O3 | Melting Point | 59-63 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 122.5±22.7 °C | |
| Name | Methyl 4-Formylbenzoate | 
|---|---|
| Synonym | More Synonyms | 
| Density | 1.2±0.1 g/cm3 | 
|---|---|
| Boiling Point | 265.0±0.0 °C at 760 mmHg | 
| Melting Point | 59-63 °C(lit.) | 
| Molecular Formula | C9H8O3 | 
| Molecular Weight | 164.158 | 
| Flash Point | 122.5±22.7 °C | 
| Exact Mass | 164.047348 | 
| PSA | 43.37000 | 
| LogP | 2.05 | 
| Vapour Pressure | 0.0±0.5 mmHg at 25°C | 
| Index of Refraction | 1.558 | 
| Stability | Stable, though possibly air-sensitive. Combustible. Incompatible with strong oxidizing agents. | 
| Water Solubility | insoluble | 
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter | 
|---|---|
| Hazard Codes | Xn: Harmful; | 
| Risk Phrases | R36/37/38 | 
| Safety Phrases | S22-S24/25 | 
| RIDADR | NONH for all modes of transport | 
| WGK Germany | 2 | 
| HS Code | 29183000 | 
| Precursor 10 | |
|---|---|
| DownStream 9 | |
| HS Code | 2918300090 | 
|---|---|
| Summary | 2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0% | 
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                                    Two main metabolites of gentiopicroside detected in rat plasma by LC-TOF-MS following 2,4-dinitrophenylhydrazine derivatization.
                                    
                                    
                                     J. Pharm. Biomed. Anal. 107 , 1-6, (2015) The metabolism of gentiopicroside in vivo was studied by LC/MS following 2,4-dinitrophenylhydrazine derivatization for the first time. The ionization efficiency of the major metabolites erythrocentaur...  | 
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                                    New analytical method for the study of metabolism of swertiamarin in rats after oral administration by UPLC-TOF-MS following DNPH derivatization.
                                    
                                    
                                     Biomed. Chromatogr. 29 , 1184-9, (2015) The metabolism of swertiamarin in vivo was studied by LC-MS following 2,4-dinitrophenylhydrazine derivatization. The ionization efficiency of the main metabolite erythrocentaurin was greatly enhanced ...  | 
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                                    Synthesis and discovery of high affinity folate receptor-specific glycinamide ribonucleotide formyltransferase inhibitors with antitumor activity.
                                    
                                    
                                     J. Med. Chem. 51 , 5052, (2008) 6-Substituted classical pyrrolo[2,3-d]pyrimidine antifolates with a three- to six-carbon bridge between the heterocycle and the benzoyl-L-glutamate (compounds 2-5, respectively) were synthesized start...  | 
                                
| METHYL PARA-FORMYLBENZOATE | 
| p-Formylbenzoic acid methyl ester | 
| p-Methoxycarbonylbenzaldehyde | 
| Methyl Terephthalaldehydate | 
| Methyl 4-formylbenzoate | 
| methyl-4-formylbenzoate | 
| 4-Formylbenzoic Acid Methyl Ester | 
| Benzoic acid, 4-formyl-, methyl ester | 
| Terephthalaldehydic Acid Methyl Ester | 
| EINECS 216-385-5 | 
| p-methoxycarbonyl benzaldehyde | 
| MFCD00006950 |