(S)-Boc-2-cyano-β-Homophe-OH
(S)-Boc-2-cyano-β-Homophe-OH (CAS: 270065-83-3) is a protected unnatural beta-amino acid derivative with the molecular formula C16H20N2O4 and a molecular weight of 304.34 g/mol. This compound serves as a valuable chiral building block in complex organic synthesis. It finds utility in peptide chemistry and the development of novel chemical entities within chemical biology and pharmaceutical research, offering unique structural modifications compared to natural amino acids.
- IUPAC
- (S)-3-(Boc-amino)-4-(2-cyanophenyl)butyric acid,Boc-2-cyano-L-β-homophenylalanine
Peptide Synthesis
Incorporates unnatural beta-amino acid residues into peptide backbones, enabling the creation of peptidomimetics with modified biological activity and stability.
Chiral Building Block
Acts as a versatile chiral synthon in asymmetric synthesis for the construction of complex organic molecules and pharmaceutical intermediates.
Chemical Biology Research
Used in the design and synthesis of novel molecules for studying biological processes and developing new therapeutic agents.
Drug Discovery
Facilitates the exploration of new chemical space in the development of drug candidates by introducing non-proteinogenic amino acid structures.
| Molecular weight | 304.34 |
|---|---|
| Empirical formula | C16H20N2O4 |
| Assay | ≥98.0% (HPLC) |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is (S)-Boc-2-cyano-β-Homophe-OH used for?
+
(S)-Boc-2-cyano-β-Homophe-OH is primarily used as a protected unnatural beta-amino acid derivative and a chiral building block in organic synthesis, particularly in peptide chemistry and chemical biology research.
What is the CAS number and molecular formula for (S)-Boc-2-cyano-β-Homophe-OH?
+
The CAS number is 270065-83-3, and the molecular formula is C16H20N2O4.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies (S)-Boc-2-cyano-β-Homophe-OH with an assay of ≥98.0% determined by HPLC. We do not represent this product as USP, BP, or EP grade.
What are the safety and handling recommendations for this compound?
+
Appropriate personal protective equipment, including eyeshields and gloves, should be worn. A type N95 (US) or type P1 (EN143) respirator filter is recommended. The compound is classified under WGK Germany 3, indicating a high hazard to water.
How is (S)-Boc-2-cyano-β-Homophe-OH packed, shipped, and exported?
+
Products are carefully packed according to industry standards for safe transport and are available for global export.
How can I request a sample or quote for (S)-Boc-2-cyano-β-Homophe-OH?
+
Please contact our sales department through the website or by phone to request a sample or obtain a quotation.
▶ Related products
1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis
1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more
3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis
3-Methyl-1,5-pentanediol
Chemical Synthesis
3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis