340138
4-Carboxybenzenesulfonazide
97%
Synonym(s):
4-(Azidosulfonyl)benzoic acid
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About This Item
Product Name
4-Carboxybenzenesulfonazide, 97%
InChI
1S/C7H5N3O4S/c8-9-10-15(13,14)6-3-1-5(2-4-6)7(11)12/h1-4H,(H,11,12)
SMILES string
OC(=O)c1ccc(cc1)S(=O)(=O)N=[N+]=[N-]
InChI key
OWULJVXJAZBQLL-UHFFFAOYSA-N
assay
97%
reaction suitability
reaction type: click chemistry
mp
180 °C (dec.) (lit.)
functional group
azide
carboxylic acid
storage temp.
2-8°C
Quality Level
Application
Synthesis of anti-inflammatory agents
Azide amidation
Reactions of thio acids with azides
Chemoselective sodium borohydride reduction of azides in water
Reagent for:
Photo-Stevens rearrangement
Cobalt-catalyzed synthesis of tertiary azides
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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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