404764
4-Acetamidobenzenesulfonyl azide
97%
Synonym(s):
p-ABSA
About This Item
Recommended Products
Assay
97%
form
solid
reaction suitability
reaction type: click chemistry
mp
107-111 °C (lit.)
functional group
amide
azide
SMILES string
CC(=O)Nc1ccc(cc1)S(=O)(=O)N=[N+]=[N-]
InChI
1S/C8H8N4O3S/c1-6(13)10-7-2-4-8(5-3-7)16(14,15)12-11-9/h2-5H,1H3,(H,10,13)
InChI key
NTMHWRHEGDRTPD-UHFFFAOYSA-N
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General description
Application
Monosaccharide-derived alcohols
Non-peptidic NK3 receptor antagonists
Reagent for:
A late-stage intermolecular C-H olefination
Intramolecular isomuenchnone cycloaddition approach to antitumor agents
Rhodium-catalyzed carbene cyclization cycloaddition cascade reaction of vinylsulfonates
Suzuki-Miyaura cross coupling reaction
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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Articles
Since the preparation of the first organic azide, phenyl azide, by Peter Griess in 1864 this energy-rich and versatile class of compounds has enjoyed considerable interest.
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