ChemicalBook--->CAS DataBase List--->25742-12-5

25742-12-5

25742-12-5 Structure

25742-12-5 Structure
IdentificationBack Directory
[Name]

5-CYANOTHIAZOLE
[CAS]

25742-12-5
[Synonyms]

5-CYANOTHIAZOLE
5-Thiazolecarbonitrile
THIAZOLE-5-CARBONITRILE
1,3-thiazole-5-carbonitrile
[Molecular Formula]

C4H2N2S
[MDL Number]

MFCD06797206
[MOL File]

25742-12-5.mol
[Molecular Weight]

110.14
Chemical PropertiesBack Directory
[Melting point ]

53 °C
[Boiling point ]

90-93 °C(Press: 15 Torr)
[density ]

1.33
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

-0.40±0.10(Predicted)
[Appearance]

Yellow to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
[Signal word ]

Warning
[Hazard statements ]

H315-H332-H319-H371-H312-H335-H302
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P-P261-P271-P304+P340-P312-P260-P264-P270-P309+P311-P405-P501-P264-P270-P301+P312-P330-P501-P280-P302+P352-P312-P322-P363-P501
[Hazard Codes ]

Xn
[Risk Statements ]

22
[HS Code ]

2934100090
Spectrum DetailBack Directory
[Spectrum Detail]

5-CYANOTHIAZOLE(25742-12-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Thiazolecarboxaldehyde,  oxime

116045-57-9

5-CYANOTHIAZOLE

25742-12-5

1,3-Thiazole-5-carboxaldehyde oxime (2.5 g, 19.5 mmol, 1 eq.) was used as a starting material, which was dissolved in 12 mL of dioxane, followed by the addition of triethylamine (TEA, 6.8 mL, 2.5 eq.). The reaction mixture was cooled to 0 °C and trifluoroacetic anhydride (3.0 mL, 1.1 eq.) was added slowly and dropwise. The reaction solution was stirred overnight at room temperature and then trifluoroacetic anhydride (1.1 eq.) was added again to ensure complete reaction. Stirring was continued overnight at room temperature followed by solvent evaporation. The residue was dissolved in dichloromethane (DCM) and washed five times with water. The organic layer was dried over anhydrous magnesium sulfate (MgSO4) and concentrated under reduced pressure to give 1.25 g of 1,3-thiazole-5-carbonitrile in 58% yield.

[References]

[1] Journal of Medicinal Chemistry, 2012, vol. 55, # 1, p. 68 - 83
[2] Patent: WO2013/60744, 2013, A2. Location in patent: Page/Page column 11; 12
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