3-Thiophenecarboxaldehyde 98.0%(GC)
98.0%(GC)
Synonym: 3-formylthiophene
Linear Formula:
C5H4OS
Molecular Weight: 112.15g/mol
CAS Number: 498-62-4
Properties
| Vapour pressure | 0.31 mm Hg ( 20 ℃) |
| Autoignition temp. | >392 ℉ |
| Assay Purity | >98%(GC) |
| Refractive index | n20/D 1.583 (lit.) |
| B pt. | 194-196 ℃ (lit.) |
| M pt. | '30℃ |
| Density | 1.28 g/mL at 25 ℃ (lit.) |
Safety Information
| Hazard Statement(s) | H315-H319-H227 |
| Precautionary Statement | P501-P210-P264-P280-P302 + P352-P370 + P378-P337 + P313-P305 + P351 + P338-P362 + P364 -P403 + P235 |
| Symbol |
|
| Signal word | Warning |
| HS Code | 2934999090 |
| Flash point | 75℃ |
| Storage Temp. | 0-10℃ |
| Storage Class | 6.1 |
| Packaging | Glass Bottle |
| UN Number | 2811 |
Description
Application
3-Thiophenecarboxaldehyde has been used in the synthesis of series of 4-substituted 2-thiophenesulfonamides acetal and ketal derivatives of 4-demethylepipodophyllotoxin--D-glucoside and epipodophyllotoxin--D-glucoside 12-di-3-thienyl-2-hydroxyethanone (33-thenoin) 3-thienyl symmetric analog of benzoin.
Purpose
For R&D use onlynot for drug household or other uses.
General Description
3-Thiophenecarboxaldehyde is used in biological studies to determine the volatile compounds formed from the interaction between organoselenium and sulfur compounds.
Documents
| SDS |
| COA |
| Specification |
| Bulk quote order form |
