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CS-W001157 4
Total: USD 88.00
  • CAS No. 3001-72-7

  • Cat. No. CS-W016569
  • Purity≥95%
  • MDL No.MFCD00005554

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

DBN|CS-W016569

Structure of 3001-72-7

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General Information

  • CAS No. 3001-72-7
  • Cat. No. CS-W016569
  • Purity ≥95%
  • MDL No. MFCD00005554
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₁₂N₂
  • Molecular Weight None
  • Synonym(s) 1,5-Diazabicyclo[4.3.0]non-5-ene; 1,5-Diazabicyclo[4.3.0]non-5-ene
  • SMILES C12=NCCCN1CCC2

Description

DBN is a strong base widely used as a catalyst in organic synthesis to facilitate Michael additions and aldol condensations.1,5-Diazabicyclo[4.3.0]non-5-ene (DBN) can be used as: A reagent for the synthesis of -carbolines from tetrahydro--carbolines via dehydrogenative/decarboxylative aromatization. A nucleophilic organocatalyst in the regioselective C-acylation of pyrroles and indoles by FriedelCrafts acylation reaction.A superbase in the formulation of a ternary liquid-liquid phase changing system, along with hexadecane and hexanol, to capture hydrogen sulfide gas. A base for the preparation of 1H-quinazoline-2,4-diones from 2-aminobenzonitriles using supercritical carbon dioxide as a reactant and a solvent. A catalyst for the synthesis of benzothiazolones by the reaction between 2-aminothiophenols and CO2 by cyclocarbonylation reaction via C-S bond formation.

Safety Information

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GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 3267
Class : 8
Packing Group : Ⅱ
Hazard Statements : H314
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501

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Computational Chemistry Data

  • TPSA   15.6
  • LogP   0.8844
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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