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15405 Sigma-Aldrich

Boc-Thr(Bzl)-OH

≥99.0% (T)

Synonym: N-(tert-Butoxycarbonyl)-O-benzyl-L-threonine, Boc-O-benzyl-L-threonine

  • CAS Number 15260-10-3

  • Linear Formula CH3CH(OCH2C6H5)CH(COOH)NHCOOC(CH3)3

  • Molecular Weight 309.36

  •  Beilstein/REAXYS Number 3065591

  •  EC Number 239-304-5

  •  MDL number MFCD00066062

  •  PubChem Substance ID 57647413

  •  NACRES NA.22

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Properties

Related Categories Amino Acids & Derivatives, Chemical Biology, Chemical Synthesis, Peptide Synthesis and Peptide Chemistry, Standard Boc Amino Acids,
assay   ≥99.0% (T)
optical activity   [α]20/D +16.5±1°, c = 1% in methanol
mp   112-114 °C (lit.)
  112-117 °C
storage temp.   2-8°C
SMILES string   C[C@@H](OCc1ccccc1)[C@H](NC(=O)OC(C)(C)C)C(O)=O
InChI   1S/C16H23NO5/c1-11(21-10-12-8-6-5-7-9-12)13(14(18)19)17-15(20)22-16(2,3)4/h5-9,11,13H,10H2,1-4H3,(H,17,20)(H,18,19)/t11-,13+/m1/s1
InChI key   CTXPLTPDOISPTE-YPMHNXCESA-N

Description

Packaging

5 g in poly bottle

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

Natural Amino Acid Building Blocks for Peptide Synthesis

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.1 Today, the most common synthetic approaches to medium and even large peptide...
Matthias Junkers
ChemFiles 2008, 8.7, 22.
Keywords: Building blocks, Peptide synthesis, Peptidomimetics, Solid phase peptide synthesis

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