CAS 3160-59-6
:N-[(Phenylmethoxy)carbonyl]-L-isoleucine
Description:
N-[(Phenylmethoxy)carbonyl]-L-isoleucine, with the CAS number 3160-59-6, is an amino acid derivative characterized by the presence of a phenylmethoxycarbonyl group attached to the isoleucine backbone. This compound features a chiral center, which contributes to its stereochemical properties, making it an L-isomer. The phenylmethoxycarbonyl group enhances the lipophilicity of the molecule, potentially influencing its solubility and reactivity in various chemical environments. It is often utilized in peptide synthesis and as a protecting group in organic synthesis due to its stability under certain conditions. The compound's structure allows for specific interactions in biological systems, which can be important for its applications in pharmaceuticals and biochemistry. Additionally, its unique functional groups may participate in hydrogen bonding and other intermolecular interactions, affecting its behavior in solution and solid states. Overall, N-[(Phenylmethoxy)carbonyl]-L-isoleucine is a valuable compound in synthetic organic chemistry and biochemistry.
Formula:C14H19NO4
InChI:InChI=1S/C14H19NO4/c1-3-10(2)12(13(16)17)15-14(18)19-9-11-7-5-4-6-8-11/h4-8,10,12H,3,9H2,1-2H3,(H,15,18)(H,16,17)/t10-,12-/m0/s1
InChI key:InChIKey=JSHXJPFZKBRLFU-JQWIXIFHSA-N
SMILES:[C@@H]([C@H](CC)C)(NC(OCC1=CC=CC=C1)=O)C(O)=O
Synonyms:- ((Benzyloxy)carbonyl)-<span class="text-smallcaps">L</span>-isoleucine
- (2S,3S)-2-{[(benzyloxy)carbonyl]amino}-3-methylpentanoate
- <span class="text-smallcaps">L</span>-Isoleucine, N-[(phenylmethoxy)carbonyl]-
- CBZ-<span class="text-smallcaps">L</span>-Isoleucine
- CBZ-L-Isoleucine
- CBZ-L-Isoleucine-OH
- Isoleucine, N-carboxy-, N-benzyl ester
- Isoleucine, N-carboxy-, N-benzyl ester, <span class="text-smallcaps">L</span>-
- N-(Benzyloxycarbonyl)isoleucine
- N-(Carbobenzyloxy)isoleucine
- N-Benzyloxycarbonyl-<span class="text-smallcaps">L</span>-isoleucine
- N-Benzyloxycarbonyl-L-isoleucine
- N-Carbobenzoxy-<span class="text-smallcaps">L</span>-isoleucine
- N-Carbobenzoxy-L-isoleucine
- N-Carbobenzyloxy-<span class="text-smallcaps">L</span>-isoleucine
- N-Cbz-L-isoleucine
- N-[(Phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-isoleucine
- N-[(benzyloxy)carbonyl]isoleucine
- Z-Ile-OH
- Z-L-isoleucine
- Z-lle-OH
- z-Ile
- Isoleucine, N-carboxy-, N-benzyl ester, L-
- N-[(Phenylmethoxy)carbonyl]-L-isoleucine
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Found 8 products.
L-Isoleucine, N-[(phenylmethoxy)carbonyl]-
CAS:Formula:C14H19NO4Purity:98%Color and Shape:LiquidMolecular weight:265.3050N-Benzyloxycarbonyl-L-isoleucine
CAS:Formula:C14H19NO4Purity:>98.0%(HPLC)Color and Shape:White or Colorless to Almost white or Almost colorless powder to lump to clear liquidMolecular weight:265.31Z-L-isoleucine
CAS:<p>Z-L-isoleucine is an amino acid that can be found in the form of a white powder. It has a low molecular weight and vapor pressure, and is soluble in water and methanol. Z-L-isoleucine is synthesized by reacting formamide with ammonium chloride to produce an acid moiety containing the desired amino acyl group. This compound can be used for gelation, solvents, supramolecular chemistry and biological properties. Z-L-isoleucine has been shown to have hydrogen bond interactions with other molecules such as water and amines, which may contribute to its biological properties as well.</p>Formula:C14H19NO4Purity:Min. 95%Color and Shape:Colourless To Pale Yellow LiquidMolecular weight:265.31 g/molZ-L-Isoleucine extrapure, 95%
CAS:Formula:C14H19NO4Purity:min. 95%Color and Shape:Clear, Pale yellow, Viscous liquidMolecular weight:265.30N-Cbz-L-isoleucine
CAS:Controlled Product<p>Applications N-Cbz-L-isoleucine is an N-Cbz-protected form of L-Isoleucine (I820175). L-Isoleucine is classified as an essential amino acid, and is also a tumour promoter of bladder cancer in rats.<br>References Hatch, T., et al.: Infect. Immun., 12, 211 (1975); Nishio, Y., et al.: Science, 231, 843 (1986)<br></p>Formula:C14H19NO4Color and Shape:NeatMolecular weight:265.30







