4-Acetamidobenzenesulfonyl azide 97%

Properties

Related Categories	Azidation/Diazo Transfer, Azides, Building Blocks, C-X Bond Formation (Non-Halogen), Chemical Biology, Chemical Synthesis, Conjugation Chemistry: Azides, Alkynes and Other Reagents, Nitrogen Compounds, Organic Azides, Organic Building Blocks, Synthetic Reagents, Various Azides More...
assay	97%
mp	107-111 °C(lit.)

Description

Packaging

5, 25 g in glass bottle

Application

Hydroazidation Catalyst for Facile Preparation of Organoazides

Diazo transfer agent.^1,^2,³

Reagent for synthesis of:
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

Price and Availability

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Related Papers

Highly convergent total synthesis of (+)-lithospermic acid via a late-stage intermolecular C-H olefination. D. Wang and J. Yu, J. Am. Chem. Soc. 133, 5767-5769, (2011)

Documents

Certificate of Analysis

Certificate of Origin

Safety Information

Symbol	GHS07
Signal word	Warning
Hazard statements	H315-H319-H335
Precautionary statements	P261-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes (Europe)	Xi
Risk Statements (Europe)	36/37/38
Safety Statements (Europe)	26-37/39
WGK Germany	3

Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Articles

Organic Azides and Azide Sources

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. In more recent years, comp...
Matthias Junkers
Aldrich ChemFiles 2008, 8.1, 10.
Keywords: Combinatorial synthesis, Cycloadditions, Hydroazidations, Metathesis, Peptide synthesis