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 1523618-35-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl trans-3-bromocyclobutane-1-carboxylate features a rigid cyclobutane core with defined stereochemistry, enabling precise control in asymmetric synthesis. The bromine substituent at the 3-position serves as a reactive handle for transition-metal-catalyzed coupling, while the ester group facilitates derivatization. This bench-stable, moisture-tolerant reagent integrates efficiently into complex molecular architectures.
Methyl trans-3-bromocyclobutane-1-carboxylate serves as a versatile chiral building block for cyclobutane-based scaffolds, enabling stereoselective functionalization via substitution or coupling reactions. The trans configuration ensures defined stereochemistry in downstream transformations, while the bromide and ester groups offer orthogonal reactivity for C–C bond formation and derivatization. Bench-stable and amenable to purification by flash chromatography, it facilitates efficient synthesis of complex cyclic systems relevant to medicinal chemistry and process development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: