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 165253-29-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-(Bromomethyl)tetrahydrofuran is a reactive, bench-stable building block featuring a primary alkyl bromide tethered to a tetrahydrofuran ring. This functionalized heterocycle enables direct incorporation into synthetic pathways requiring electrophilic alkylation or chain extension. The bromomethyl group facilitates efficient coupling reactions under mild conditions, while the cyclic ether framework provides solubility and structural rigidity.
3-(Bromomethyl)tetrahydrofuran serves as a versatile bifunctional building block, enabling efficient alkylation and coupling reactions in synthetic organic chemistry. The bromomethyl group exhibits high reactivity toward nucleophiles under mild conditions, while the tetrahydrofuran ring provides excellent solubility and stability. Its compatibility with various functional groups facilitates integration into complex molecular architectures, including heterocyclic scaffolds and pharmaceutical intermediates.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: