(S)-2-(Boc-amino)-3-phenyl-1-propanol
(S)-2-(Boc-amino)-3-phenyl-1-propanol (CAS 66605-57-0) is a protected amino alcohol with a molecular weight of 251.32 g/mol. This chiral compound, featuring the phenylalaninol backbone protected with a Boc group, is primarily utilised as a building block in chemical synthesis. It is particularly valuable in the creation of biochemically active molecules and in peptide chemistry, offering a defined stereochemical centre for complex organic constructions.
- IUPAC
- (S)-(−)-2-(tert-Butoxycarbonylamino)-3-phenyl-1-propanol,N-(tert-Butoxycarbonyl)-L-phenylalaninol,Boc-L-phenylalaninol
- Synonyms
- N-(tert-Butoxycarbonyl)-L-phenylalaninolBoc-L-phenylalaninol(S)-(−)-2-(tert-Butoxycarbonylamino)-3-phenyl-1-propanol
![(S)-2-(Boc-amino)-3-phenyl-1-propanol (C6H5CH2CH[NHCO2C(CH3)3]CH2OH) — chemical structure, CAS 66605-57-0; Chemistry, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F66605-57-0.png&w=3840&q=75)
Synthesis of Biochemically Active Compounds
This compound serves as a key intermediate in the multi-step synthesis of various biologically relevant molecules. Its defined stereochemistry is crucial for building complex structures with specific physiological activities.
Peptide Chemistry
The Boc-protected amino alcohol moiety makes it suitable for incorporation into peptide chains, particularly where modified amino acid residues are required. It facilitates the formation of peptide bonds under controlled conditions.
Chiral Building Block
As a chiral molecule, it is employed in asymmetric synthesis to introduce specific stereocentres into target molecules. This is essential in the development of stereospecific pharmaceuticals and agrochemicals.
| Molecular weight | 251.32 |
|---|---|
| Linear formula | C6H5CH2CH[NHCO2C(CH3)3]CH2OH |
| Assay | 98% |
| Optical activity | [α]20/D −27°, c = 1 in chloroform |
| Optical purity | ee: 99% (GLC) |
| Application | Employed in the synthesis of biochemically active compounds. For references, see Aldrichimica Acta.1 |
| Melting point | 94-96 °C(lit.) |
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)-2-(Boc-amino)-3-phenyl-1-propanol used for?
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It is primarily used as a building block in chemical synthesis, particularly for creating biochemically active compounds and in peptide chemistry due to its chiral nature and Boc protecting group.
What is the CAS number and chemical formula for this compound?
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The CAS number is 66605-57-0. The linear formula is C 6 H 5 CH 2 CH[NHCO 2 C(CH 3 ) 3 ]CH 2 OH.
What grade and purity does Tech Serve Solutions supply?
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Tech Serve Solutions supplies this compound with an assay of 98% and high optical purity (ee: 99%). It is supplied as a research-grade chemical and TSS does not represent it as USP, BP, or EP grade.
How should (S)-2-(Boc-amino)-3-phenyl-1-propanol be handled?
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This compound has a WGK Germany classification of 3, indicating it is hazardous. Handle with appropriate personal protective equipment in a well-ventilated area, avoiding contact with skin, eyes, and clothing, and preventing dust formation.
Is this compound regulated or controlled?
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The provided data does not indicate that this compound is specifically controlled or scheduled under common regulations. However, always consult current local and international regulations for precise handling and reporting requirements.
How is this chemical packed, shipped, and exported?
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Tech Serve Solutions securely packs chemicals in compliance with international shipping regulations for safe transport. We are experienced exporters, handling all necessary documentation for global distribution.
How can I request a sample or a quote?
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To request a sample or a quote, please contact our sales team through the website or by direct email, providing the product name and CAS number (66605-57-0) for prompt processing.
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