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 18156-67-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(2-Bromoethyl)trimethylsilane delivers a reactive bromoethyl handle tethered to a stable trimethylsilyl group, enabling efficient silicon-directed functionalization. This bench-stable reagent facilitates site-selective derivatization in synthetic and bioconjugation workflows.
(2-Bromoethyl)trimethylsilane serves as a versatile silyl-protected bromoethyl building block, enabling efficient introduction of reactive bromoalkyl handles under mild conditions. Its trimethylsilyl group provides enhanced stability and facilitates selective deprotection, while the terminal bromide supports reliable coupling reactions with nucleophiles, including amines and thiols. This reagent functions effectively in the synthesis of heterocyclic scaffolds and functionalized intermediates, offering predictable reactivity and ease of purification in standard organic workflows.
|
GHS Pictogram :
|
GHS No : GHS02,GHS05
|
|
Signal Word : Danger
|
UN#: 2924
|
|
Class : 3,8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H225-H314
|
|
|
Precautionary Statements : P210-P233-P240-P242-P243-P260-P264-P280-P301+P330+P331-P304+P340-P363-P370+P378-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: