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 16793-90-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This bromoalkylated aromatic compound features a reactive 2-bromoethyl handle attached to a methyl-substituted benzene ring. The electrophilic bromide enables efficient coupling in nucleophilic substitution reactions, while the alkyl chain provides synthetic flexibility for building complex architectures. Bench-stable and compatible with standard reaction conditions.
1-(2-Bromoethyl)-2-methylbenzene serves as a versatile alkylating agent in synthetic organic chemistry, enabling efficient introduction of the 2-bromoethyl motif into diverse substrates. Its benzylic bromide functionality exhibits high reactivity in SN₂ reactions and facilitates C–C bond formation under mild conditions. The molecule’s bench stability and compatibility with common functional groups make it suitable for constructing complex 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: