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 626-35-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl nitroacetate has been used in:synthesis of -oxoacids via Michael addition reaction with ,-unsaturated ketonesfuctionalization of C4-position on pyrimidine and C6-position on 2-deoxyguanosine to produce novel nucleosides facile synthesis of ,-diisobutylglycinesynthesis of DL-4,4-difluoroglutamic acid
Ethyl nitroacetate serves as a versatile synthon in organic synthesis, enabling efficient access to α-nitro carbonyl compounds and nitroalkanes through standard condensation and reduction protocols. Its bench-stable nature and compatibility with diverse functional groups facilitate reliable use in multistep sequences, particularly in the construction of heterocyclic scaffolds and nitrogen-containing building blocks for medicinal chemistry applications.
|
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: