Boc-N-Me-Nle-OH
Boc-N-Me-Nle-OH (CAS: 117903-25-0; Formula: C12H23NO4) is a N-methylated, N-Boc protected derivative of the non-proteinogenic amino acid norleucine. With a molecular weight of 245.32 g/mol, this compound serves as a valuable building block in organic synthesis, particularly in peptide chemistry and medicinal chemistry research. Its protected nature facilitates controlled reactions, making it suitable for complex molecular constructions.
- IUPAC
- Boc-N-methyl-L-norleucine,Boc-menle-oh
- Synonyms
- Boc-N-methyl-L-norleucine,Boc-menle-oh

Peptide Synthesis
Boc-N-Me-Nle-OH is utilised as a protected amino acid derivative in solid-phase and solution-phase peptide synthesis. Its N-methyl modification can introduce specific conformational constraints into peptide chains.
Medicinal Chemistry
This compound serves as a key building block for the synthesis of novel drug candidates and biologically active molecules. Its incorporation can modulate pharmacokinetic properties and receptor binding.
Organic Synthesis
As a functionalized chiral molecule, it finds application in the construction of complex organic structures and as a starting material for various chemical transformations.
| Molecular weight | 245.32 |
|---|---|
| Empirical formula | C12H23NO4 |
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 Boc-N-Me-Nle-OH used for?
+
Boc-N-Me-Nle-OH is primarily used as a protected amino acid building block in peptide synthesis, medicinal chemistry research, and general organic synthesis.
What is the CAS number and formula for Boc-N-Me-Nle-OH?
+
The CAS number for Boc-N-Me-Nle-OH is 117903-25-0, and its molecular formula is C12H23NO4.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Boc-N-Me-Nle-OH for research and development purposes. The specific assay and grade are available on the product's Certificate of Analysis. We do not represent this product as USP, BP, EP, or for any pharmaceutical, nutraceutical, food, or cosmetic use.
What are the safety considerations for handling Boc-N-Me-Nle-OH?
+
Boc-N-Me-Nle-OH is classified under GHS07 with hazard statements including H315 (Causes skin irritation), H319 (Causes serious eye irritation), and H335 (May cause respiratory irritation). Handle with appropriate personal protective equipment in a well-ventilated area.
Is Boc-N-Me-Nle-OH a controlled substance?
+
Based on the provided data, Boc-N-Me-Nle-OH is not listed as a controlled substance.
How is Boc-N-Me-Nle-OH packed, shipped, and exported?
+
Boc-N-Me-Nle-OH is carefully packed according to industry standards to ensure safe transit. Tech Serve Solutions is an experienced global exporter of chemicals, adhering to all relevant shipping and customs regulations.
How can I request a sample or a quote for Boc-N-Me-Nle-OH?
+
To request a sample or obtain a quote for Boc-N-Me-Nle-OH, please contact our sales department through the website or by phone, referencing the product name and CAS number.
▶ 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