N-Boc-L-felinine

Base Information

• Chemical Name: N-Boc-L-felinine
• CAS No.: 879207-98-4
• Molecular Formula: C₁₃H₂₅NO₅S
• Molecular Weight: 307.411
• DSSTox Substance ID: DTXSID80572497
• Wikidata: Q82460858
• Mol file: 879207-98-4.mol

Synonyms:N-Boc-L-felinine;879207-98-4;L-Cysteine,N-[(1,1-dimethylethoxy)carbonyl]-S-(3-hydroxy-1,1-dimethylpropyl)-;(2R)-3-(4-hydroxy-2-methylbutan-2-yl)sulfanyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid;DTXSID80572497;AKOS030254498;N-(tert-Butoxycarbonyl)-S-(4-hydroxy-2-methylbutan-2-yl)-L-cysteine;(R)-2-((tert-Butoxycarbonyl)amino)-3-((4-hydroxy-2-methylbutan-2-yl)thio)propanoic acid;(R)-2-((tert-Butoxycarbonyl)amino)-3-((4-hydroxy-2-methylbutan-2-yl)thio)propanoicacid

Chemical Property of N-Boc-L-felinine

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.512
• Boiling Point: 466.05°C at 760 mmHg
• Flash Point: 235.659°C
• PSA: 121.16000
• Density: 1.173g/cm³
• LogP: 2.24940
• Solubility.: Acetonitrile, Chloroform, Methanol
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 9
• Exact Mass: 307.14534407
• Heavy Atom Count: 20
• Complexity: 338

Purity/Quality:

97% ^*data from raw suppliers

N-Boc-L-felinine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)OC(=O)NC(CSC(C)(C)CCO)C(=O)O
• Isomeric SMILES: CC(C)(C)OC(=O)N[C@@H](CSC(C)(C)CCO)C(=O)O
• Uses: An intermediate for the synthesis of Felinine An intermediate for the synthesis of Felinine.

Technology Process of N-Boc-L-felinine

There total 1 articles about N-Boc-L-felinine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

C13H23NO5S → C13H25NO5S (879207-98-4)

Guidance literature:

With sodium tetrahydroborate; In acetonitrile; for 1h;

DOI:10.1021/jf063453h

Reference yield:

C13H25NO5S (879207-98-4) → L-felinine (471-09-0)

Guidance literature:

With hydrogenchloride;

DOI:10.1021/jf063453h

Downstream raw materials:

L-felinine

Refernces