Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 19311-37-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Bromotetrahydrofuran is a reactive, bench-stable heterocyclic building block featuring a pendant bromide at the 3-position. This electrophilic site enables efficient coupling reactions in synthetic sequences, particularly in transition-metal-catalyzed transformations. The saturated furan ring provides structural rigidity and enhanced solubility in common organic solvents.
3-Bromotetrahydrofuran serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized heterocycles and pharmaceutical intermediates. Its well-established reactivity facilitates nucleophilic substitution and transition-metal-catalyzed coupling reactions, offering high regioselectivity and compatibility with diverse functional groups. The compound exhibits excellent bench stability and is readily purified by standard techniques, making it ideal for scalable synthesis and iterative molecular construction in medicinal and process chemistry workflows.
|
GHS Pictogram :
|
GHS No : GHS02
|
|
Signal Word : Danger
|
UN#: 1993
|
|
Class : 3
|
Packing Group : Ⅲ
|
|
Hazard Statements : H226-H315-H319-H335
|
|
|
Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: