(S)-(−)-N-Boc-tert-leucinol
(S)-(−)-N-Boc-tert-leucinol (CAS: 153645-26-2) is a chiral amino alcohol derivative with the linear formula (CH3)3CCH(CH2OH)NHCO2C(CH3)3 and a molecular weight of 217.31. It is commonly employed as a building block in organic synthesis, particularly in the fields of peptide chemistry and chemical biology. This compound is supplied by TSS with an assay of ≥98%.

Chiral Building Block in Organic Synthesis
Utilised as a key chiral intermediate for the stereoselective synthesis of complex organic molecules. Its structure makes it valuable for introducing specific stereochemistry into target compounds.
Peptide Chemistry
Serves as a component in the synthesis of modified peptides or peptidomimetics, contributing unique structural features and potentially influencing biological activity.
Chemical Biology Research
Employed in studies within chemical biology, where chiral molecules are often essential for understanding biological interactions and developing new biochemical tools.
Pharmaceutical Intermediate Development
Acts as a precursor or intermediate in the multi-step synthesis of active pharmaceutical ingredients (APIs), contributing to the development of novel therapeutics.
| Molecular weight | 217.31 |
|---|---|
| Linear formula | (CH3)3CCH(CH2OH)NHCO2C(CH3)3 |
| Assay | ≥98% |
| 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)-(−)-N-Boc-tert-leucinol used for?
+
(S)-(−)-N-Boc-tert-leucinol is primarily used as a chiral building block in organic synthesis, with applications in peptide chemistry, chemical biology, and pharmaceutical intermediate development.
What is the CAS number and chemical formula for (S)-(−)-N-Boc-tert-leucinol?
+
The CAS number is 153645-26-2 and the linear formula is (CH3)3CCH(CH2OH)NHCO2C(CH3)3.
What grade and purity does Tech Serve Solutions supply for (S)-(−)-N-Boc-tert-leucinol?
+
Tech Serve Solutions supplies (S)-(−)-N-Boc-tert-leucinol with an assay of ≥98%. TSS does not represent this product as USP, BP, EP or other pharmacopoeial grades unless explicitly stated in the specifications.
What are the safety and handling precautions for (S)-(−)-N-Boc-tert-leucinol?
+
Handling requires appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter should be used if airborne exposure is a risk. The product has a WGK Germany classification of 3, indicating a high hazard.
How is (S)-(−)-N-Boc-tert-leucinol packed and shipped?
+
Tech Serve Solutions exports fine chemicals globally. Specific packing and shipping details for (S)-(−)-N-Boc-tert-leucinol will be provided upon request, adhering to all relevant international regulations for chemical transport.
How can I request a sample or quote for (S)-(−)-N-Boc-tert-leucinol?
+
To request a sample or a quotation for (S)-(−)-N-Boc-tert-leucinol, please contact the Tech Serve Solutions sales team through our official website or by direct enquiry, referencing the product name and CAS number 153645-26-2.
▶ 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