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CS-W001157 4
Total: USD 88.00

(-)-Menthol

  • CAS No. 2216-51-5

  • Cat. No. CS-M3737
  • Purity≥98%
  • MDL No.MFCD00062979

*For research and further manufacturing use only, not for direct human use.

(-)-Menthol|CS-M3737

Structure of 2216-51-5

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General Information

  • CAS No. 2216-51-5
  • Cat. No. CS-M3737
  • Purity ≥98%
  • MDL No. MFCD00062979
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₂₀O
  • Molecular Weight 156.27
  • Synonym(s) None
  • SMILES O[C@H]1[C@H](C(C)C)CC[C@@H](C)C1

Description

H-Lys(Z)-OH also known as N6-carbobenzyloxy-L-lysine, commonly used as a reagent in the synthesis of peptides.H-Lys(Z)-OH serves as a reactant for the synthesis of various peptides such as boc-Glu(OBzl)-Lys(Z)-OH and tert-butyl-6-(((benzyloxy)carbonyl)amino)-2-bromohexanoate. Additionally, it is used in the Fuchs-Farthing method to synthesize lysine NCA, which is a block copolymer.

Synthesis

  • Route1

    References

    • Justus Liebigs Annalen der Chemie, , vol. 624, p. 142,202
  • Route2
    • null|null
      110-82-7
    • null|null
      13947-22-3
    • null|null
      676-54-0
    • ~%
    • null|null
      91695-29-3
    • In-stock
      (-)-Menthol|CS-M3737
      2216-51-5
    • null|null
      106-97-8

    References

    • Journal fuer Praktische Chemie (Leipzig), , vol. <2> 151, p. 61,62
  • Route3
    • null|null
      64-17-5
    • In-stock
      (1R,2S,5R)-2-Isopropyl-5-methylcyclohexanamine|CS-0886535
      2216-54-8
    • null|null
      64-19-7
    • ~%
    • null|null
      61585-35-1
    • In-stock
      (-)-Menthol|CS-M3737
      2216-51-5
    • null|null
      13947-22-3
    • null|null
      13947-22-3

    References

    • Journal fuer Praktische Chemie (Leipzig), , vol. <2>158, p. 21,30

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319
Precautionary Statements : P264-P280-P302+P352

Quality Control

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Computational Chemistry Data

  • TPSA   20.23
  • LogP   2.4395
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   1

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