O-Phenyl chlorothionoformate
98%
- Product Code: 97378
Alias:
Chloromethyl phenylthioformate Chloromethylthiophenyl thiochloroformate-O-phenyl
CAS:
1005-56-7
| Molecular Weight: | 172.63 g./mol | Molecular Formula: | C₇H₅ClOS |
|---|---|---|---|
| EC Number: | 213-736-4 | MDL Number: | MFCD00004920 |
| Melting Point: | Boiling Point: | 81-83 °C6 mm Hg(lit.) | |
| Density: | 1.248 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C, dry, sealed |
Product Description:
O-Phenyl chlorothionoformate is primarily used in organic synthesis as a versatile reagent for introducing the phenylthio group into various compounds. It is particularly valuable in the preparation of thioesters, which are intermediates in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it serves as a key building block in the production of sulfur-containing heterocycles, which are important in medicinal chemistry for developing drugs with potential therapeutic applications. Its reactivity with nucleophiles makes it useful in cross-coupling reactions and the modification of biomolecules, aiding in the study of biochemical pathways and the development of novel bioactive compounds.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 97.5 100% |
| AGNO3 | 96.5 101.5% |
| REFRACTIVE INDEX N20D | 1.58-1.583 |
| SPECIFIC GRAVITY 2020 | 1.276-1.279 |
| APPEARANCE | CLEAR YELLOW TO YELLOW GREEN LIQUID |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $22.10 |
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| 5.000 | 10-20 days | $59.27 |
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| 25.000 | 10-20 days | $262.18 |
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| 100.000 | 10-20 days | $904.07 |
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O-Phenyl chlorothionoformate
O-Phenyl chlorothionoformate is primarily used in organic synthesis as a versatile reagent for introducing the phenylthio group into various compounds. It is particularly valuable in the preparation of thioesters, which are intermediates in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it serves as a key building block in the production of sulfur-containing heterocycles, which are important in medicinal chemistry for developing drugs with potential therapeutic applications. Its reactivity with nucleophiles makes it useful in cross-coupling reactions and the modification of biomolecules, aiding in the study of biochemical pathways and the development of novel bioactive compounds.
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