Azetidine, 98%, Thermo Scientific Chemicals
Azetidine, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Azetidine, 98%, Thermo Scientific Chemicals

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Quantity:
1 g
250 mg
5 g
Catalog number H56351.03
also known as H56351-03
Price (USD)/ Each
142.65
Online exclusive
158.00 
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Quantity:
1 g
Request bulk or custom format
Price (USD)/ Each
142.65
Online exclusive
158.00 
Save 15.35 (10%)
Add to cart
Azetidine, 98%, Thermo Scientific Chemicals
Catalog numberH56351.03
Price (USD)/ Each
142.65
Online exclusive
158.00 
Save 15.35 (10%)
-
Add to cart
Chemical Identifiers
CAS503-29-7
IUPAC Nameazetidine
Molecular FormulaC3H7N
InChI KeyHONIICLYMWZJFZ-UHFFFAOYSA-N
SMILESC1CNC1
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SpecificationsSpecification SheetSpecification Sheet
Assay (unspecified)>97.5%
Azetidine is involved in a high yielding palladium-catalyzed cross-coupling reaction with aryl bromides. Further, it is used in Ullmann type coupling reaction with iodonitroflourenes. In addition to this, it reacts with bis-(3-amino-propyl)-amine to prepare N,N'-bis-(3-amino-propyl)-propanediyldiamine using palladium as a catalyst.

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.

Applications
Azetidine is involved in a high yielding palladium-catalyzed cross-coupling reaction with aryl bromides. Further, it is used in Ullmann type coupling reaction with iodonitroflourenes. In addition to this, it reacts with bis-(3-amino-propyl)-amine to prepare N,N′-bis-(3-amino-propyl)-propanediyldiamine using palladium as a catalyst.

Solubility
Miscible with water.

Notes
Store in a cool place. Keep the container tightly closed in a dry and well-ventilated place. Air sensitive and heat sensitive. Incompatible with strong oxidizing agents and strong acids.
RUO – Research Use Only

General References:

  1. Nassoy, A. C. M. A.; Raubo, P.; Harrity, J. P. A. Synthesis and indole coupling reactions of azetidine and oxetane sulfinate salts. Chem. Commun. 2015, 51 (27), 5914-5916.
  2. Ding, F.; William, R.; Kock, S. M.; Leow, M. L.; Liu, X. W. A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B. Chem. Commun. 2015, 51, 4639-4642.