(S)-Boc-4-methyl-β-Homophe-OH
(S)-Boc-4-methyl-β-Homophe-OH, identified by CAS number 270062-96-9 and molecular formula C16H23NO4, is a protected unnatural amino acid derivative. This compound, with a molecular weight of 293.36 g/mol, is primarily utilised in chemical synthesis and peptide chemistry. Its structure makes it a valuable building block for creating complex peptides and other organic molecules in research and development settings.
- IUPAC
- (S)-3-(Boc-amino)-4-(4-methylphenyl)butyric acid,Boc-4-methyl-L-β-homophenylalanine

Peptide Synthesis
Serves as a crucial unnatural amino acid building block for incorporating modified structures into peptide chains, enabling research into novel peptide therapeutics and peptidomimetics.
Chemical Synthesis
A versatile intermediate in organic synthesis, particularly for the construction of complex molecules where a chiral, protected beta-amino acid moiety is required.
Chemical Biology Research
Used in the development of modified peptides and small molecules for probing biological pathways and understanding protein-ligand interactions.
| Molecular weight | 293.36 |
|---|---|
| Empirical formula | C16H23NO4 |
| Assay | ≥97.0% (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-4-methyl-β-Homophe-OH used for?
+
This compound is primarily used as a building block in peptide synthesis and as an intermediate in chemical synthesis, particularly for creating unnatural amino acid derivatives and complex organic molecules.
What is the CAS number and formula for (S)-Boc-4-methyl-β-Homophe-OH?
+
The CAS number is 270062-96-9 and the molecular formula is C16H23NO4.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies (S)-Boc-4-methyl-β-Homophe-OH with an assay of ≥97.0% (HPLC). This is a research-grade material and is not represented as USP, BP, EP, or pharmacopoeia grade.
How should (S)-Boc-4-methyl-β-Homophe-OH be handled?
+
Handle with appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter is recommended. Refer to the safety data sheet for comprehensive handling instructions.
Is this compound a controlled substance?
+
The provided data does not indicate that (S)-Boc-4-methyl-β-Homophe-OH is a controlled substance.
How is this chemical packed and shipped?
+
Products are carefully packed to ensure stability during transit and are exported globally by Tech Serve Solutions in compliance with international shipping regulations for chemicals.
How can I request a quote or sample?
+
To request a quote or sample of (S)-Boc-4-methyl-β-Homophe-OH, please contact our sales team through the website or by phone.
▶ 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