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15528 Sigma-Aldrich

Boc-Val-OH

≥99.0% (T)

Synonym: (S)-2-(Boc-amino)-3-methylbutyric acid, N-(tert-Butoxycarbonyl)-L-valine, Boc-L-valine

  • CAS Number 13734-41-3

  • Linear Formula (CH3)2CHCH(COOH)NHCOOC(CH3)3

  • Molecular Weight 217.26

  •  Beilstein/REAXYS Number 1711290

  •  EC Number 237-307-6

  •  MDL number MFCD00065605

  •  eCl@ss 32160406

  •  PubChem Substance ID 57647474

  •  NACRES NA.22

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Properties

Related Categories Amino Acids & Derivatives, C-H Activation, Catalysis and Inorganic Chemistry, Chemical Biology, Chemical Synthesis,
Quality Level   100
assay   ≥99.0% (T)
optical activity   [α]20/D −6.2±0.5°, c = 1% in acetic acid
reaction suitability   reaction type: C-H Activation
  reagent type: ligand
reaction type: Peptide Synthesis
application(s)   peptide synthesis: suitable
mp   77-80 °C (lit.)
functional group   amine
  carboxylic acid
SMILES string   CC(C)[C@H](NC(=O)OC(C)(C)C)C(O)=O
InChI   1S/C10H19NO4/c1-6(2)7(8(12)13)11-9(14)15-10(3,4)5/h6-7H,1-5H3,(H,11,14)(H,12,13)/t7-/m0/s1
InChI key   SZXBQTSZISFIAO-ZETCQYMHSA-N

Description

Packaging

25, 100 g in glass bottle

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

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

Peer-Reviewed Papers
15

References

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