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4-Acetamidobenzenesulfonyl azide, 97%, Thermo Scientific Chemicals
CAS: 2158-14-7 | C8H8N4O3S | 240.24 g/mol
$58.52 - $238.03
Chemical Identifiers
| CAS | 2158-14-7 |
|---|---|
| Molecular Formula | C8H8N4O3S |
| Molecular Weight (g/mol) | 240.24 |
| MDL Number | MFCD00029626 |
| InChI Key | NTMHWRHEGDRTPD-UHFFFAOYSA-N |
| Synonym | 4-acetamidobenzenesulfonyl azide, p-absa, n-4-azidosulfonylphenyl acetamide, 4-acetamidobenzenesulfonylazide, 4-acetamidobenzenesulphonyl azide, 4-acetamidobenzene sulfonyl azide, 4-acetamidobenzene-1-sulfonyl azide, acmc-1chyo, ksc491c8r, p-acetamidobenzensulfonyl azide |
| PubChem CID | 5129185 |
| IUPAC Name | N-(4-azidosulfonylphenyl)acetamide |
| SMILES | CC(=O)NC1=CC=C(C=C1)S(=O)(=O)N=[N+]=[N-] |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAL1591606
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Thermo Scientific Chemicals
L1591606 |
5 g |
Each for $58.52
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AAL1591614
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Thermo Scientific Chemicals
L1591614 |
25 g |
Each for $238.03
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Description
4-Acetamidobenzenesulfonyl azide is used as a hydroazidation catalyst for facile preparation of organoazides. It is used as a reagent for synthesis of: monosaccharide-derived alcohols, a late-stage intermolecular C-H olefination, intramolecular isomuenchnone cycloaddition approach to antitumor agents, rhodium-catalyzed carbene cyclization cycloaddition cascade reaction of vinylsulfonates and Suzuki-Miyaura cross coupling reaction.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications4-Acetamidobenzenesulfonyl azide is used as a hydroazidation catalyst for facile preparation of organoazides. It is used as a reagent for synthesis of: monosaccharide-derived alcohols, a late-stage intermolecular C-H olefination, intramolecular isomuenchnone cycloaddition approach to antitumor agents, rhodium-catalyzed carbene cyclization cycloaddition cascade reaction of vinylsulfonates and Suzuki-Miyaura cross coupling reaction.
Solubility
Insoluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
Chemical Identifiers
| 2158-14-7 | |
| 240.24 | |
| NTMHWRHEGDRTPD-UHFFFAOYSA-N | |
| 5129185 | |
| CC(=O)NC1=CC=C(C=C1)S(=O)(=O)N=[N+]=[N-] |
| C8H8N4O3S | |
| MFCD00029626 | |
| 4-acetamidobenzenesulfonyl azide, p-absa, n-4-azidosulfonylphenyl acetamide, 4-acetamidobenzenesulfonylazide, 4-acetamidobenzenesulphonyl azide, 4-acetamidobenzene sulfonyl azide, 4-acetamidobenzene-1-sulfonyl azide, acmc-1chyo, ksc491c8r, p-acetamidobenzensulfonyl azide | |
| N-(4-azidosulfonylphenyl)acetamide |
Specifications
| 2158-14-7 | |
| C8H8N4O3S | |
| 5 g | |
| 4-acetamidobenzenesulfonyl azide, p-absa, n-4-azidosulfonylphenyl acetamide, 4-acetamidobenzenesulfonylazide, 4-acetamidobenzenesulphonyl azide, 4-acetamidobenzene sulfonyl azide, 4-acetamidobenzene-1-sulfonyl azide, acmc-1chyo, ksc491c8r, p-acetamidobenzensulfonyl azide | |
| NTMHWRHEGDRTPD-UHFFFAOYSA-N | |
| N-(4-azidosulfonylphenyl)acetamide | |
| 5129185 | |
| 97% |
| 107°C to 111°C | |
| MFCD00029626 | |
| 2219568 | |
| Insoluble in water. | |
| CC(=O)NC1=CC=C(C=C1)S(=O)(=O)N=[N+]=[N-] | |
| 240.24 | |
| 240.24 | |
| 4-Acetamidobenzenesulfonyl azide |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
EINECSNumber : 606-801-7
TSCA : No
Recommended Storage : Store at -20°C
RUO – Research Use Only