ChemicalBook--->CAS DataBase List--->7552-07-0

7552-07-0

7552-07-0 Structure

7552-07-0 Structure
IdentificationMore
[Name]

5-Amino-1,2,4-thiadiazole
[CAS]

7552-07-0
[Synonyms]

1,2,4-THIADIAZOL-5-AMINE
1,2,4-THIADIAZOL-5-YLAMINE
5-AMINO-1,2,4-THIADIAZOLE
1,2,4-Thiadiazole, 5-amino-
1,2,4-Thiadiazol-5-amine(9CI)
[Molecular Formula]

C2H3N3S
[MDL Number]

MFCD01102171
[Molecular Weight]

101.13
[MOL File]

7552-07-0.mol
Questions And AnswerBack Directory
[Physical Form]

Solid
Chemical PropertiesBack Directory
[Melting point ]

112-115°C
[Boiling point ]

238.9±23.0 °C(Predicted)
[density ]

1.495±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

solid
[pka]

3.97±0.50(Predicted)
[color ]

Yellow
[InChI]

InChI=1S/C2H3N3S/c3-2-4-1-5-6-2/h1H,(H2,3,4,5)
[InChIKey]

VJHTZTZXOKVQRN-UHFFFAOYSA-N
[SMILES]

S1C(N)=NC=N1
[CAS DataBase Reference]

7552-07-0(CAS DataBase Reference)
[NIST Chemistry Reference]

5-Amino-1,2,4-thiadiazole(7552-07-0)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

20/22
[HazardClass ]

IRRITANT
[HS Code ]

2934999090
Hazard InformationBack Directory
[Uses]

5-Amino-1,2,4-thiadiazole is a useful research chemical for organic synthesis and other chemical processes.
[Synthesis]

Thiourea, N-[(dimethylamino)methylene]-, [N(E)]-

943653-32-5

5-Amino-1,2,4-thiadiazole

7552-07-0

The general procedure for the synthesis of 5-amino-1,2,4-thiadiazole from the compound (CAS: 943653-32-5) is as follows: (E)-N'-carbamoyl-N,N-dimethylformamide (3.9 g, 30 mmol), hydroxylamine-O-sulphonic acid (3.7 g, 33 mmol) were mixed with anhydrous ethanol (100 mL) and reacted by heating at 80 °C for for 8 hours. Upon completion of the reaction, the mixture was cooled to room temperature, triethylamine was added and stirring was continued at room temperature for 19 hours. Subsequently, the solvent was removed by distillation under reduced pressure, and the residue was dissolved in a mixture of dichloromethane and methanol (10 mL) with a volume ratio of 9:1. Dichloromethane solution containing 5% methanol was used as the eluent, and purification was carried out by silica gel column chromatography, resulting in 1 ,2,4-thiadiazol-5-amine as a white solid (1.4 g, 47% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 7.95 (s, 2H), 7.85 (s, 1H).LC/MS analysis conditions: 10%-99% acetonitrile (containing 0.035% trifluoroacetic acid)/water (containing 0.05% trifluoroacetic acid), observed m/z (M+1) = 102.1; retention time tR = 0.39 min.

[References]

[1] Patent: US2009/124655, 2009, A1. Location in patent: Page/Page column 14
[2] Patent: US2009/131440, 2009, A1. Location in patent: Page/Page column 18-19
[3] Patent: US2008/27067, 2008, A1. Location in patent: Page/Page column 259
Spectrum DetailBack Directory
[Spectrum Detail]

5-Amino-1,2,4-thiadiazole(7552-07-0)1HNMR
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