CAS 42918-86-5
:(2S)-2-[[(Phenylmethoxy)carbonyl]amino]butanoic acid
Description:
(2S)-2-[[(Phenylmethoxy)carbonyl]amino]butanoic acid, also known by its CAS number 42918-86-5, is an amino acid derivative characterized by its specific stereochemistry and functional groups. This compound features a butanoic acid backbone with a phenylmethoxycarbonyl group attached to the amino group, which contributes to its unique properties. The presence of the phenyl group enhances its hydrophobic characteristics, while the carboxylic acid group provides acidic properties, allowing for potential interactions in biological systems. The stereochemistry at the second carbon (2S) indicates that it has a specific spatial arrangement, which is crucial for its biological activity and interactions with enzymes or receptors. This compound may be of interest in pharmaceutical applications, particularly in the design of peptide-based drugs or as a building block in organic synthesis. Its solubility and reactivity can vary based on the pH and the presence of other functional groups, making it a versatile compound in chemical research and development.
Formula:C12H15NO4
InChI:InChI=1/C12H15NO4/c1-2-10(11(14)15)13-12(16)17-8-9-6-4-3-5-7-9/h3-7,10H,2,8H2,1H3,(H,13,16)(H,14,15)/t10-/m0/s1
InChI key:InChIKey=SZQMTCSQWUYUML-JTQLQIEISA-N
SMILES:C(OC(N[C@H](C(O)=O)CC)=O)C1=CC=CC=C1
Synonyms:- (2S)-2-[[(Phenylmethoxy)carbonyl]amino]butanoic acid
- (2S)-2-{[(benzyloxy)carbonyl]amino}butanoic acid
- (S)-2-(((Benzyloxy)carbonyl)amino)butanoic acid
- (S)-2-(Benzyloxycarbonylamino)butyric acid
- (S)-Cbz-2-aminobutyric acid
- 2-{[(Benzyloxy)Carbonyl]Amino}Butanoic Acid
- <span class="text-smallcaps">L</span>-Cbz-Aminobutyric acid
- Butanoic acid, 2-[[(phenylmethoxy)carbonyl]amino]-, (2S)-
- Butanoic acid, 2-[[(phenylmethoxy)carbonyl]amino]-, (S)-
- NSC 164666
- Z-D-Abu-OH
- N-ALPHA-CARBOBENZOXY-L-ALPHA-AMINO-BUTYRIC ACID
- Z-L-ALPHA-AMINOBUTYRIC ACID
- 2-(phenylmethoxycarbonylamino)butanoic acid
- 02906
- Z-L-2Abu-OH
- Cbz-2-Abu-OH
- Z-NHCH(CH2CH3)-COOH
- Z-L-α-aminobutyric acid
- CBZ-L-ABU-OH
- Cbz-Abu-OH
- Z-ABU(2)-OH
- Nsc164666
- Z-2-ABU-OH
- Z-2-AMINOBUTYRIC ACID
- Z-ABU(ALPHA)-OH
- (S)-2-(bezyloxycarbonylamino)butanoic acid
- Z-L-α-aminobutyric acid≥ 98% (HPLC)
- Z-L-Abu-OH
- Z-2-AMINOBUTYRIC ACID extrapure
- CBZ-L-2-AMINOBUTYRIC ACID
- Z-AMINOBUTYRIC ACID
- (S)-2-(Benzyloxycarbonylamino)butanoic acid
- N-α-Cbz-2- aminoisobutyricacid
- Z-ABU-OH
- Z-D-Abu
- Z-2-Abu-OH(Z-2-aMinobutyric acid)
- Z-ALPHA-ABU-OH
- Z-L-2-AMINOBUTANOIC ACID
- N-Benzyloxycarbonyl-L-2-aminobutyric acid
- N-ALPHA-CARBOBENZOXY-L-2-AMINO-BUTANOIC ACID
- Z-L-2-aminobutyric acid
- (S)-2-(Cbz-amino)butyric Acid
- Z-ABU-OH USP/EP/BP
- BENZYLOXYCARBONYL-L-2-AMINOBUTYRIC ACID
- (S)-2-(Benzyloxycarbonylamino)butyricacid,98%
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Found 7 products.
(S)-2-(Benzyloxycarbonylamino)butyric acid, 98%
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:C12H15NO4Purity:98%Molecular weight:237.26Z-Abu-OH
CAS:<p>Z-Abu-OH</p>Formula:C12H15NO4Purity:98%Color and Shape: off-white solidMolecular weight:237.25g/molZ-2-Aminobutyric Acid extrapure, 99%
CAS:Formula:C12H15NO4Purity:min. 99%Color and Shape:White to Off White, PowderMolecular weight:237.30Z-Abu-OH
CAS:<p>M06083 - Z-Abu-OH</p>Formula:C12H15NO4Purity:98%Color and Shape:SolidMolecular weight:237.255(S)-2-(((Benzyloxy)carbonyl)amino)butanoic Acid
CAS:Controlled ProductFormula:C12H15NO4Color and Shape:NeatMolecular weight:290.314Z-L-alpha-aminobutyric acid
CAS:<p>Z-L-alpha-aminobutyric acid is a homogeneous, optically active, linear phosphinic analogue of alpha-aminobutyric acid. It has been used in the synthesis of phosphinic analogues of cyclosporin and undecapeptides with high yields. The coupling reaction between Z-L-alpha-aminobutyric acid and benzaldehyde was carried out in two steps to produce the desired product. A stepwise condensation between Z-L-alpha-aminobutyric acid and 3,4,5,6 tetrahydropyrimidine was also successful.</p>Formula:C12H15NO4Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:237.25 g/mol






