| Weight | 265.309 g/mol |
|---|---|
| Formula | C14H19NO4 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
Boc-Phe-OH (13734-34-4)
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- Synthesis, crystal structure, and molecular conformation of peptide N-Boc-L-Pro-dehydro-Phe-L-Gly-OH (Biopolymers, 1990)
- A general route to carba peptide bond replacements: Unequivocal synthesis of Boc-L-Phe-(CH2-CH2)-L-Ala-OH and Boc-L-Phe-(CH2-CH2)-D-Ala-OH. (Tetrahedron Letters, 1990)
- (2S,5S,8S,11S)-1-Acetyl-1,4-diaza-3-keto-5-carboxy-10-thia-tricyclo -[2.8.04,8]-tridecane, 1 the preferred conformation of 1 (1 Temp-OH) and its peptide conjugates Temp-L-(Ala)n-OR (n=1 to 4) and -Temp-L-Ala-L-Phe-L-Lys(Boc)-L-Lys(-Boc)-NHMe studies of templates for -helix formation (Tetrahedron Letters, 1988)
- Carba peptide bond surrogates: synthesis of Boc-L-Leu-(CH2-CH2)-L-Phe-OH and Boc-LLeu--(CH2-CH2)-D-Phe-OH through a horner-emmons reaction. (Tetrahedron Letters, 1990)
- Helix termination and chain reversal: crystal and molecular structure of the alpha, beta-dehydrooctapeptide Boc-Val-DeltaPhe-Phe-Ala-Leu-Ala-DeltaPhe-Leu-OH. (Journal of Biomolecular Structure & Dynamics, 1996)
- Preparation of carba dipeptides bearing a basic side-chain at the C-terminus: synthesis of enantiopure Boc-d-Phe-[CH2CH2]-l-Arg(NO2)-OH and Boc-d-Phe-[CH2CH2]-d-Arg(NO2)-OH (Tetrahedron Letters, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
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SMILESCC(C)(C)OC(=O)NC(CC1=CC=CC=C1)C(=O)O
-
InChIKeyZYJPUMXJBDHSIF-UHFFFAOYSA-N
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