Name | 5-Nitrothiophene-2-carboxaldehyde |
Synonyms | AKOS 93853 LABOTEST-BB LT00112375 5-NITROTHIOPHENE-2-CARBALDEHYDE 5-Nitrothiophene-2-carbaldehyde 5-NITRO-2-THIOPHENECARBALDEHYDE 5-Nitrothiophene-2-carboxaldehyde 5-NITROTHIOPHENE-2-CARBOXALDEHYDE 5-NITRO-2-THIOPHENECARBOXALDEHYDE 2-METHYL-6-(DICHLOROMETHYL)PYRIDINE HCL |
CAS | 4521-33-9 |
EINECS | 224-850-9 |
InChI | InChI=1/C5H3NO3S/c7-3-4-1-2-5(10-4)6(8)9/h1-3H |
InChIKey | CHTSWZNXEKOLPM-UHFFFAOYSA-N |
Molecular Formula | C5H3NO3S |
Molar Mass | 157.15 |
Density | 1.534±0.06 g/cm3(Predicted) |
Melting Point | 75-77 °C (lit.) |
Boling Point | 118-120 °C(Press: 3-4 Torr) |
Flash Point | 133.5°C |
Water Solubility | Insoluble in water. |
Solubility | acetone: soluble1%, clear, yellow |
Vapor Presure | 0.00137mmHg at 25°C |
Appearance | Solid |
Color | Brown |
BRN | 120540 |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Sensitive | Air Sensitive |
Refractive Index | 1.662 |
MDL | MFCD00005433 |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
HS Code | 29349990 |
introduction | thiophene compounds have pharmacological activities such as antibacterial, anti-inflammatory, antiviral and antispasmodic. studying their effects with bovine serum albumin (BSA) is of great significance to the understanding of their pharmacokinetics and the development of new drugs. 5-nitrothiophene-2-formaldehyde is an important intermediate in organic synthesis. It can be used as a pharmaceutical intermediate in the pharmaceutical industry, and can also be used as a raw material to synthesize a series of nitrothiophene Schiff bases. |
preparation | 0.1 mol5-chloro -2-nitrobenzaldehyde, 0.005mol palladium acetate and 0.006mol 1,10-phenanthroline are dissolved in 20 mL N, N-dimethylformamide, then 0.15mmol hexahydropyridine is added dropwise, stirred at 60 ℃ for 24 hours, poured into water, extracted with ethyl acetate, and recrystallized to obtain 5-nitrothiophene -2-formaldehyde, the yield is 63%. |