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 25662-28-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 1-cyclopentene-1-carboxylate features a strained cyclopentene ring fused to an ester group, enabling direct participation in Diels-Alder reactions. The electron-deficient alkene serves as a potent dienophile, pairing efficiently with dienes under mild conditions. This bench-stable reagent delivers high regioselectivity and enables rapid access to functionalized cyclohexene derivatives in synthetic sequences.
Methyl 1-cyclopentene-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cyclopentane derivatives. Its conjugated enoate functionality facilitates Diels-Alder reactions, Michael additions, and transition-metal-catalyzed couplings. The ester group provides a handle for selective reduction or hydrolysis, while the cyclopentenyl scaffold offers structural rigidity beneficial in medicinal chemistry and natural product synthesis. Bench-stable and readily purified by distillation or chromatography, it supports scalable transformations in both academic and industrial R&D workflows.
|
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: