CAS 2650-64-8
:N2-[(Phenylmethoxy)carbonyl]-L-glutamine
Description:
N2-[(Phenylmethoxy)carbonyl]-L-glutamine, with the CAS number 2650-64-8, is a derivative of the amino acid L-glutamine, characterized by the presence of a phenylmethoxycarbonyl group at the nitrogen atom of the amine side chain. This modification enhances its stability and solubility, making it useful in various biochemical applications. The compound typically exhibits properties associated with amino acids, such as being polar and capable of forming hydrogen bonds, which can influence its reactivity and interaction with biological systems. It is often utilized in peptide synthesis and as a building block in the development of pharmaceuticals. The presence of the phenylmethoxy group may also impart unique characteristics, such as increased lipophilicity, which can affect its bioavailability and transport across biological membranes. Overall, N2-[(Phenylmethoxy)carbonyl]-L-glutamine serves as an important compound in organic synthesis and medicinal chemistry, contributing to the design of more effective therapeutic agents.
Formula:C13H16N2O5
InChI:InChI=1S/C13H16N2O5/c14-11(16)7-6-10(12(17)18)15-13(19)20-8-9-4-2-1-3-5-9/h1-5,10H,6-8H2,(H2,14,16)(H,15,19)(H,17,18)/t10-/m0/s1
InChI key:InChIKey=JIMLDJNLXLMGLX-JTQLQIEISA-N
SMILES:C(OC(N[C@@H](CCC(N)=O)C(O)=O)=O)C1=CC=CC=C1
Synonyms:- (2S)-2-[[(Benzyloxy)carbonyl]amino]-4-carbamoylbutanoic acid
- (2S)-5-Amino-5-oxo-2-(phenylmethoxycarbonylamino)pentanoic acid
- (2S)-5-amino-2-{[(benzyloxy)carbonyl]amino}-5-oxopentanoate
- <span class="text-smallcaps">L</span>-Glutamine, N<sup>2</sup>-[(phenylmethoxy)carbonyl]-
- Benzyloxycarbonyl-<span class="text-smallcaps">L</span>-glutamine
- BenzyloxycarbonylLglutamine
- Carbobenzoxy-<span class="text-smallcaps">L</span>-glutamine
- Cbz-<span class="text-smallcaps">L</span>-glutamine
- Cbz-Gln-OH
- Cbz-L-glutamine
- Glutamine, N<sup>2</sup>-carboxy-, N-benzyl ester
- Glutamine, N<sup>2</sup>-carboxy-, N<sup>2</sup>-benzyl ester, <span class="text-smallcaps">L</span>-
- N(alpha)-Benzyloxycarbonyl-L-glutamine
- N(alpha)-Cbz-L-glutamine
- N-(Benzyloxycarbonyl)-<span class="text-smallcaps">L</span>-glutamine
- N-Carbobenzoxy-<span class="text-smallcaps">L</span>-glutamine
- N-cbz-L-glutamine crystalline
- N2-[(benzyloxy)carbonyl]-L-glutamine
- N2-[(benzyloxy)carbonyl]glutamine
- N<sup>2</sup>-Benzoxycarbonyl-<span class="text-smallcaps">L</span>-glutamine
- N<sup>2</sup>-Benzyloxycarbonyl-<span class="text-smallcaps">L</span>-glutamine
- N<sup>2</sup>-Carbobenzoxy-<span class="text-smallcaps">L</span>-glutamine
- N<sup>2</sup>-[(Phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-glutamine
- N<sup>α</sup>-Benzyloxycarbonyl-<span class="text-smallcaps">L</span>-glutamine
- NSC 186903
- Z-Gln-OH
- Z-L-Glutamine
- z-Gln
- Glutamine, N2-carboxy-, N-benzyl ester
- Carbobenzoxy-L-glutamine
- N2-[(Phenylmethoxy)carbonyl]-L-glutamine
- Glutamine, N2-carboxy-, N2-benzyl ester, L-
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 9 products.
N-Carbobenzoxy-L-glutamine
CAS:Formula:C13H16N2O5Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:280.28N(α)-Benzyloxycarbonyl-L-glutamine, 99%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C13H16N2O5Purity:99%Color and Shape:Powder, WhiteMolecular weight:280.28Z-Gln-OH
CAS:<p>Substrate for Bacillus circulans peptidoglutaminase.</p>Formula:C13H16N2O5Purity:> 99%Color and Shape:WhiteMolecular weight:280.28L-Glutamine, N2-[(phenylmethoxy)carbonyl]-
CAS:Formula:C13H16N2O5Purity:95%Color and Shape:SolidMolecular weight:280.2765N-Carbobenzyloxy-L-glutamine
CAS:<p>N-Carbobenzyloxy-L-glutamine</p>Purity:95%Molecular weight:280.28g/molCbz-L-glutamine
CAS:<p>Cbz-L-glutamine is a water soluble compound that is used in the synthesis of pomalidomide. It is synthesized through a stepwise amide formation from methylamine and ethylene diamine. Cbz-L-glutamine has been shown to have an inhibitory effect on cancer cells, which may be due to its ability to break down hydroxamic acids. This chemical reaction causes the release of hydrogen ions, which leads to the disruption of various cellular processes, such as DNA replication and protein synthesis. The uptake of Cbz-L-glutamine by cancer cells has been shown in tissue culture experiments.</p>Formula:C13H16N2O5Purity:Min. 95%Color and Shape:PowderMolecular weight:280.28 g/molZ-Gln-OH
CAS:<p>M03034 - Z-Gln-OH</p>Formula:C13H16N2O5Purity:97%Color and Shape:Solid, White to off-white powderMolecular weight:280.28Z-L-Glutamine extrapure, 99%
CAS:Formula:C13H16N2O5Purity:min. 99 %Color and Shape:White, Crystalline powderMolecular weight:280.30








