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2-Aminothiazole

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Revision as of 14:14, 20 December 2010 by CheMoBot (talk | contribs) (Updating {{chembox}} (changes to watched fields - added verified revid - updated 'StdInChI_Ref', 'StdInChIKey_Ref') per Chem/Drugbox validation (report [[Wikipedia_talk:WikiProject_Chemicals|erro)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)
2-Aminothiazole
File:2-Aminothiazole.png
Names
IUPAC name 1,3-thiazol-2-amine
Other names 2-Thiazolamine, Aminothiazole, 2-Thiazylamine, Basedol, 2-Thiazolylamine, 4-Thiazolin-2-onimine, 2-Amino-1,3-thiazole, Abadole
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.002.284 Edit this at Wikidata
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C3H4N2S/c4-3-5-1-2-6-3/h1-2H,(H2,4,5)Key: RAIPHJJURHTUIC-UHFFFAOYSA-N
  • InChI=1/C3H4N2S/c4-3-5-1-2-6-3/h1-2H,(H2,4,5)Key: RAIPHJJURHTUIC-UHFFFAOYAZ
SMILES
  • c1csc(n1)N
Properties
Chemical formula C3H4N2S
Molar mass 100.14 g·mol
Appearance light yellow crystals
Melting point 86 - 89 °C
Boiling point 117 °C (20 hPa)
Solubility in water 100 g/l (20 °C)
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2 0 0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

2-Aminothiazole is a heterocyclic amine with odor similar to pyridine, soluble in water, alcohol and ether. It is a beginning point for synthesis of many compounds including sulfur drugs, biocides, fungicides, dyes and chemical reaction accelerators. 2-Aminothiazole can be used as a thyroid inhibitor in the treatment of hyperthyroidism and it has antibacterial activity.

External links

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