| 2-Thiophenecarbonyl chloride Basic information |
| Product Name: | 2-Thiophenecarbonyl chloride |
| Synonyms: | AKOS 92490;AKOS BBS-00003924;ALPHA-THENOYL CHLORIDE;THIOPHENE-2-CARBOXYLIC ACID CHLORIDE;THIOPHENE-2-CARBONYL CHLORIDE;TIMTEC-BB SBB004099;2-Thiophenzoyl Chloride;2-thienylcarbonyl chloride |
| CAS: | 5271-67-0 |
| MF: | C5H3ClOS |
| MW: | 146.59 |
| EINECS: | 226-092-4 |
| Product Categories: | Building Blocks;C4 to C6;ACIDHALIDE;Chemical Synthesis;Heterocyclic Building Blocks;Thiophenes;Thiophene&Benzothiophene;Heterocyclic Compounds |
| Mol File: | 5271-67-0.mol |
| 2-Thiophenecarbonyl chloride Chemical Properties |
| Boiling point | 206-208 °C (lit.) |
| density | 1.371 g/mL at 25 °C (lit.) |
| refractive index | n |
| Fp | 195 °F |
| storage temp. | 2-8°C |
| solubility | Chloroform |
| form | Liquid |
| Specific Gravity | 1.371 |
| color | Clear colorless to yellow-gray |
| Sensitive | Moisture Sensitive |
| BRN | 110145 |
| InChIKey | QIQITDHWZYEEPA-UHFFFAOYSA-N |
| CAS DataBase Reference | 5271-67-0(CAS DataBase Reference) |
| NIST Chemistry Reference | 2-Thiophenecarbonyl chloride(5271-67-0) |
| EPA Substance Registry System | 2-Thiophenecarbonyl chloride (5271-67-0) |
| Safety Information |
| Hazard Codes | C |
| Risk Statements | 34-37 |
| Safety Statements | 26-36/37/39-45 |
| RIDADR | UN 3265 8/PG 2 |
| WGK Germany | 3 |
| F | 8 |
| TSCA | Yes |
| HazardClass | 8 |
| PackingGroup | II |
| HS Code | 29349990 |
| MSDS Information |
| Provider | Language |
|---|---|
| Thiophene-2-carbonyl chloride | English |
| SigmaAldrich | English |
| ACROS | English |
| ALFA | English |
| 2-Thiophenecarbonyl chloride Usage And Synthesis |
| Chemical Properties | CLEAR COLOURLESS TO YELLOW-GREY LIQUID |
| Uses | 2-Thiophenecarbonyl Chloride is used in the synthesis of substituted pyridines as selective and highly effective GPR119 agonists. It is also seen in the preparation of diuretics. |
| Uses | 2-Thiophenecarbonyl chloride was used in the synthesis of building blocks derived from ornithine by undergoing acylation/sulphonation of copper complex of orthinine. |
| General Description | The postfunctionalization reaction of 2-thiophenecarbonyl chloride with single walled carbon nanotubes (SWCNTs) was studied. |
| 2-Thiophenecarbonyl chloride Preparation Products And Raw materials |
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