127906
5-Amino-1,3,4-thiadiazole-2-thiol
95%
Sinonimo/i:
2-Amino-5-mercapto-1,3,4-thiadiazole
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About This Item
Formula empirica (notazione di Hill):
C2H3N3S2
Numero CAS:
Peso molecolare:
133.20
Beilstein:
81728
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Saggio:
95%
Prodotti consigliati
Saggio
95%
Punto di fusione
235 °C (dec.) (lit.)
Stringa SMILE
Nc1nnc(S)s1
InChI
1S/C2H3N3S2/c3-1-4-5-2(6)7-1/h(H2,3,4)(H,5,6)
GDGIVSREGUOIJZ-UHFFFAOYSA-N
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Applicazioni
5-amino-1,3,4-thiadiazole-2-thiol was used to prepare new amines exhibiting anti-convulsant activity[1].
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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Chun-Wei Lee et al.
Biosensors & bioelectronics, 133, 215-222 (2019-04-06)
Early diagnosis of bacterial infections is crucial to improving survival rates by enabling treatment with appropriate antibiotics within the first few hours of infection. This paper presents a highly sensitive amperometric biosensor for the detection of several pathogenic bacterial cells
M Kavlakova et al.
Arzneimittel-Forschung, 62(12), 599-602 (2012-10-25)
The coordination properties of Pt(II) with 5-amino-1,3,4-thiadiazole-2-thiol [CAS 2349-67-9] (L 1 ) and its novel violurate adduct (L 2 ), both in solution and in solid state, are studied by means of conventional IR-spectroscopy, single crystal X-ray diffraction and thermal
Mohammad Hossein Ghanbari et al.
Mikrochimica acta, 186(9), 641-641 (2019-08-25)
A nanocomposite was prepared with reduced graphene oxide, gold nanoparticles and an electropolymerized film made from 2-amino-5-mercapto-1,3,4-thiadiazole. An electrochemical sensor for doxorubicin (DOX) was constructed by modifying a glassy carbon electrode (GCE) with the nanocomposite. The modified GCE was studied
Rodica Olar et al.
Materials (Basel, Switzerland), 13(20) (2020-10-22)
The derivatives 5,7-dimethyl[1,3,4]thiadiazolo[3,2-a]pyrimidin-4-ium-2-thiolate (1) and 7-methyl-5-phenyl[1,3,4]thiadiazolo[3,2-a]pyrimidin-4-ium-2-thiolate (2) were fully characterized by single-crystal X-ray diffraction. Their supramolecular structure is built through both π-π stacking and C=S-π interactions for both compounds. The embedment of the tested compounds into Fe3O4@C18 core-shell nanocoatings increased
Mohammad Yusuf et al.
Chemical biology & drug design, 81(5), 666-673 (2013-01-31)
New imines, derived from aromatic aldehyde, chalcones and 5-amino-1,3,4-thiadiazole-2-thiol exhibited promising anti-convulsant activity which is explained through chemo-biological interactions at receptor site producing the inhibition of human Carbonic Anhydrase-II enzyme (hCA-II) through the proposed pharmacophore model at molecular levels as
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