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 16672-87-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(S)-6-Oxo-2-piperidinecarboxylic acid can be used as a reactant to synthesize: Functionalized -lactam N-heterocycles via carboxymethylproline synthase catalyzed cyclization reactions. Pro-(S)-C5 branched [4.3.1] aza-amide bicycles as potential inhibitors for FK506-binding proteins. Ethyl (S)-2-(6-oxopiperidin-2-yl)acetate, which is reduced using LiBH4 to produce optically pure hydroxymethyl lactams.
|
GHS Pictogram :
|
GHS No : GHS05,GHS06,GHS09
|
|
Signal Word : Danger
|
UN#: 2923
|
|
Class : 8 (6.1)
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H311-H314-H318-H332-H402-H411
|
|
|
Precautionary Statements : P260-P261-P264-P270-P271-P273-P280-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P330-P361+P364-P363-P391-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: