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Isocyanoacetic acid potassium salt

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Isocyanoacetic acid potassium salt Basic information

Product Name:
Isocyanoacetic acid potassium salt
Synonyms:
  • Isocyanoacetic acid potassium salt
  • Potassium 2-isocyanoacetate
  • Potassium 2-isocyanoacetate technical grade, 85%
CAS:
58948-98-4
MF:
C3H2KNO2
MW:
123.15178
Product Categories:
  • Building Blocks
  • C-C Bond Formation
  • Chemical Synthesis
  • Isocyanides
  • Nitrogen Compounds
  • Organic Building Blocks
  • Others
  • Synthetic Reagents
Mol File:
58948-98-4.mol
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Isocyanoacetic acid potassium salt Chemical Properties

Melting point:
75-81 °C
form 
powder
InChI
1S/C3H3NO2.K/c1-4-2-3(5)6;/h2H2,(H,5,6);/q;+1/p-1
InChIKey
IWTQNSMPJLXKLL-UHFFFAOYSA-M
SMILES
[K+].[O-]C(=O)C[N+]#[C-]
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36/37
RIDADR 
UN 3335
WGK Germany 
3
Storage Class
11 - Combustible Solids
Hazard Classifications
Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
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Isocyanoacetic acid potassium salt Usage And Synthesis

Uses

Reagent for:• ;Carbene insertion reactions as a cleanup procedure to remove ruthenium carbene catalysts from metathesis reaction products1• ;Preparation of carbonyl complexes of group IVB metals2• ;Preparation of peptides via ammonium chloride-promoted Ugi reaction3

Uses

Reagent for:

  • Carbene insertion reactions as a cleanup procedure to remove ruthenium carbene catalysts from metathesis reaction products
  • Preparation of carbonyl complexes of group IVB metals
  • Preparation of peptides via ammonium chloride-promoted Ugi reaction

reaction suitability

reaction type: C-C Bond Formation

Isocyanoacetic acid potassium saltSupplier

Sigma-Aldrich
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