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15386 Aldrich

Boc-Asp(OBzl)-OH

≥99.0% (sum of enantiomers, HPLC)

Synonym: N-(tert-Butoxycarbonyl)-L-aspartic acid 4-benzyl ester, Boc-L-aspartic acid 4-benzyl ester

  • CAS Number 7536-58-5

  • Linear Formula C6H5CH2OCOCH2CH(COOH)NHCOOC(CH3)3

  • Molecular Weight 323.34

  •  Beilstein Registry Number 2064127

  •  EC Number 231-406-8

  •  MDL number MFCD00065564

  •  PubChem Substance ID 57647403

  •  eCl@ss 32160406

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Properties

Related Categories Amino Acids & Derivatives, Aspartic Acid, Chemical Biology, Chemical Synthesis, Peptide Chemistry More...
InChI Key   SOHLZANWVLCPHK-LBPRGKRZSA-N
assay   ≥99.0% (sum of enantiomers, HPLC)
optical activity   [α]20/D −20.0±1°, c = 2% in DMF
mp   98-102 °C(lit.)

Description

Packaging

5, 25 g in glass bottle

Price and Availability


Cross-Coupling Guide
Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

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
Aldrich ChemFiles 2008, 8.7, 22.
Keywords: Building blocks, Chemfiles, Methods, Peptide synthesis, Peptidomimetics, Solid phase peptide synthesis

Peer-Reviewed Papers
15

References

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