161602-47-7
161602-47-7
Chemical Structure
Boc-L-Ala-OH-d3
- CAS No.: 161602-47-7
- Formula:C8H12D3NO4
- Molecular Weight:192.23
IUPAC Name: (tert-butoxycarbonyl)-L-alanine-3,3,3-d3
InChIKey: QVHJQCGUWFKTSE-MQBGRFPLSA-N
SMILES: CC(C)(C)OC(N[C@@H](C([2H])([2H])[2H])C(O)=O)=O
Biological Activity: Boc-L-Ala-OH-d3 is the deuterium labeled Boc-L-Ala-OH[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Boc-L-Ala-OH-d3 | Boc-L-Ala-OH-d3 is the deuterium labeled Boc-L-Ala-OH. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Boc-L-Ala-OH-d4 | Boc-L-Ala-OH-d4 is the deuterium labeled Boc-L-Ala-OH. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Boc-Ala-OH-1-13C | 99.0% | Boc-Ala-OH-1-13C is the 13C labeled Boc-Ala-OH. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Boc-L-Ala-OH-3-13C | Boc-L-Ala-OH-3-13C is a 13C-labeled Boc-L-Ala-OH (HY-41121). Boc-L-Ala-OH (Boc-Ala-OH) shows excellent affinity with ATP. Boc-L-Ala-OH contains an amino acid moiety, and an acylamide bond like that of the peptide and protein. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Boc-L-Ala-OH-15N | Boc-L-Ala-OH-15N is the 15N labeled Boc-L-Ala-OH. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Boc-L-Ala-OH-d | Boc-L-Ala-OH-d is the deuterium labeled Boc-L-Ala-OH. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Boc-L-Ala-OH-2-13C | Boc-L-Ala-OH-2-13C is a 13C-labeled Boc-L-Ala-OH (HY-41121). Boc-L-Ala-OH (Boc-Ala-OH) shows excellent affinity with ATP. Boc-L-Ala-OH contains an amino acid moiety, and an acylamide bond like that of the peptide and protein. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Boc-L-Ala-OH | 99.07% | Boc-L-Ala-OH (Boc-Ala-OH) is a single N-protected amino acid ligand and a protected L-alanine derivative. Boc-L-Ala-OH promotes Pd (II)-catalyzed enantioselective C-H alkenylation and kinetic resolution. Boc-L-Ala-OH serves as a coupling reagent for the synthesis of liver-targeted glycogen phosphorylase inhibitors and P6A metabolites, and also acts as a negative control in synthesis studies of betulinic acid amino acid esters. Boc-L-Ala-OH is applicable to research on epidermoid squamous cell carcinoma. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
