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AMINOMALONONITRILE P-TOLUENESULFONATE

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AMINOMALONONITRILE P-TOLUENESULFONATE Basic information

Product Name:
AMINOMALONONITRILE P-TOLUENESULFONATE
Synonyms:
  • DICYANOMETHYLAMMONIUM P-TOLUENESULFONATE
  • Animomalononitrile p-toluenosulfunic acid
  • 2-Aminomalononitrile-4-methylbenzenesulphonate
  • AMINOMALONONITRILE P-TOLUENESULFONATE, 9 8%
  • AMINOMALONONITRILE 4-TOLUENESULFONATE
  • AMINOMALONONITRILE P-TOLUENESULFONATE
  • AMINOMALONONITRILE P-TOLUENESULFONIC ACID
  • AMINOMALONONITRILE P-TOLUENESULFUNIC ACID
CAS:
5098-14-6
MF:
C10H11N3O3S
MW:
253.28
EINECS:
225-817-1
Product Categories:
  • C1 to C5
  • Chemical Synthesis
  • Aromatic Esters
  • C1 to C5
  • Nitrogen Compounds
  • Organic Building Blocks
  • Cyanides/Nitriles
  • Nitrogen Compounds
  • Building Blocks
Mol File:
5098-14-6.mol
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AMINOMALONONITRILE P-TOLUENESULFONATE Chemical Properties

Melting point:
174 °C (dec.) (lit.)
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
form 
Solid
color 
Beige Powder,
Water Solubility 
almost transparency
BRN 
4050747
Stability:
Hygroscopic
CAS DataBase Reference
5098-14-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22
Safety Statements 
36
RIDADR 
3439
WGK Germany 
3
HazardClass 
6.1
PackingGroup 
III
HS Code 
2926907090

MSDS

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AMINOMALONONITRILE P-TOLUENESULFONATE Usage And Synthesis

Uses

Aminomalononitrile p-toluenesulfonate was used in the syntheiss of 1-substituted 5-amino-4-cyano-2-hydroxyimidazoles.

Uses

Aminomalononitrile p-toluenesulfonate is a reagent for diazonamide synthesis via heck endocyclization. It may also have implications for developing IκB Kinase-β inhibitors.

Purification Methods

It forms colourless crystals on recrystallisation from MeCN (1.8g in 100mL) using activated charcoal. Wash the crystals with dry Et2O and dry them at 25o/1mm. Recovery is ~80%. [Ferris et al. Org Synth Coll Vol V 32 1973.]

AMINOMALONONITRILE P-TOLUENESULFONATESupplier

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