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CS-W001157 4
Total: USD 88.00

N,N′-Di-tert-butylcarbodiimide

  • CAS No. 691-24-7

  • Cat. No. CS-0122588
  • Molecule weight154.25
  • Purity≥98%
  • MDL No.MFCD00010231

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

N,N′-Di-tert-butylcarbodiimide|CS-0122588

Structure of 691-24-7

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General Information

  • CAS No. 691-24-7
  • Cat. No. CS-0122588
  • Purity ≥98%
  • MDL No. MFCD00010231
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₈N₂
  • Molecular Weight 154.25
  • Synonym(s) N,N'-di-tert-Butylcarbodiimide
  • SMILES CC(N=C=NC(C)(C)C)(C)C

Description

N,N-Di-tert-butylcarbodiimide can be used:As a reagent for the guanylation of aryl amines catalyzed by lanthanum amides.To prepare dichloroimidazolidine-4,5-dione by reacting with oxalyl chloride, which is a key intermediate for the synthesis of N,N-diamidocarbenes.To prepare the iridium complex of benzamidine named Ir(FMeppy)2(N,N-di-tert-butyl-4-methyl-benzamidine).

Synthesis

  • Route1

    References

    • Kim, Sunggak; Yi, Kyu Yang Journal of Organic Chemistry, 1986 , vol. 51, # 13 p. 2613 - 2615
  • Route2
    • null|null
      119072-55-8
    • null|null
      75-64-9
    • ~9%
    • In-stock
      N,N′-Di-tert-butylcarbodiimide|CS-0122588
      691-24-7
    • In-stock
      N,N'-Di(tert-butyl)urea|CS-0206763
      5336-24-3

    References

    • Journal of Organic Chemistry, , vol. 78, # 7 p. 3009 - 3020
  • Route3

    References

    • Schlama; Gouverneur; Mioskowski Tetrahedron Letters, 1996 , vol. 37, # 39 p. 7047 - 7048

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS02,GHS07
Signal Word : Warning
UN#: 1993
Class : 3
Packing Group : Ⅲ
Hazard Statements : H226-H315-H319-H335
Precautionary Statements : P210-P233-P240-P241-P242-P243-P260-P264-P271-P280-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P370+P378-P403+P235-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   24.72
  • LogP   2.7573
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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