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359653 Sigma-Aldrich

Boc-Ile-OH

98%

Synonym: N-(tert-Butoxycarbonyl)-L-isoleucine, Boc-L-isoleucine

  • CAS Number 13139-16-7

  • Linear Formula CH3CH2CH(CH3)CH(COOH)NHCOOC(CH3)3

  • Molecular Weight 231.29

  •  Beilstein/REAXYS Number 1711700

  •  EC Number 236-074-8

  •  MDL number MFCD00038324

  •  eCl@ss 32160406

  •  PubChem Substance ID 24862095

  •  NACRES NA.22

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Properties

Related Categories Amino Acids & Derivatives, C-H Activation, Catalysis and Inorganic Chemistry, Chemical Biology, Chemical Synthesis,
InChI Key   QJCNLJWUIOIMMF-YUMQZZPRSA-N
assay   98%
optical activity   [α]20/D +2.7°, c = 2 in acetic acid
mp   66-69 °C (lit.)
functional group   amine
  carboxylic acid
reaction suitability   reaction type: C-H Activation
  reagent type: ligand
reaction type: Peptide Synthesis

Description

Packaging

25 g in glass bottle

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
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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