AMINOMALONONITRILE P-TOLUENESULFONATE

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

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)

Safety Information

MSDS Information

Provider	Language
SigmaAldrich	English
ALFA	English

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-TOLUENESULFONATE Preparation Products And Raw materials

Raw materials	Propanedinitrile,2-(hydroxyimino)--->p-Toluenesulfonic acid-->Malononitrile
Preparation Products	2-Pyrazinecarbonitrile , 3-amino-6-ethyl-, 4-oxide

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