2-氨基-5-苯基-1,3,4-噻二唑

小分子

5-苯基-1,3,4-噻二唑-2-胺

MLS000532026 | 2-amino-5-phenyl-[1,3,4]thiadiazole | 2-amino-5-phenyl-[1,3,4]-thiadiazole | Cambridge id 5314822 | NCGC00346710-03 | NSC 677 | Sodium iodide I 131 (USAN:USP:INN) | 2-amino-5-phenyl-1,3,4-thiadiazol | SR-01000632959-1 | DTXSID80277076 | 1,3

2-Amino-5-phenyl-1,3,4-thiadiazol

A151014-1g

1g

≥98%

充氩

常规运输

对空气敏感

2-Amino-5-phenyl-1,3,4-thiadiazole on condensation with benzaldehyde (SPT), 4-nitrobenzaldehyde (SNT), 4-methoxybenzaldehyde (SMT), 2-hydroxybenzaldehyde (SSTH) or 2-hydroxyacetophenone affords Schiff′s bases. Its molecular geometry and vibrational frequencies have been evaluated using the Hartree-Fock and density functional method (B3LYP). 2-Amino-5-phenyl-1,3,4-thiadiazole has been reported to inhibit the corrosion of mild steel in 0.5M H2SO4 and 1.0M HCl. Corrosion inhibition has been examined using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). 2-Amino-5-phenyl-1,3,4-thiadiazole on condensation with benzaldehyde (SPT), 4-nitrobenzaldehyde (SNT), 4-methoxybenzaldehyde (SMT), 2-hydroxybenzaldehyde (SSTH) or 2-hydroxyacetophenone affords Schiff′s bases. Its molecular geometry and vibrational frequencies have been evaluated using the Hartree-Fock and density functional method (B3LYP). 2-Amino-5-phenyl-1,3,4-thiadiazole has been reported to inhibit the corrosion of mild steel in 0.5M H2SO4 and 1.0M HCl. Corrosion inhibition has been examined using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS).

2-Amino-5-phenyl-1,3,4-thiadiazole may be used for the synthesis of 1,3,4-thiadiazole derivatives.

2002-03-1

C8H7N3S

177.23 g/mol

MFCD00205278

219408

C1=CC=C(C=C1)C2=NN=C(S2)N

5-phenyl-1,3,4-thiadiazol-2-amine

1S/C8H7N3S/c9-8-11-10-7(12-8)6-4-2-1-3-5-6/h1-5H,(H2,9,11)

UHZHEOAEJRHUBW-UHFFFAOYSA-N

C1=CC=C(C=C1)C2=NN=C(S2)N

488188642

可溶于二甲基甲酰胺

223-230 °C

1

4

1

177.036 Da

177.036 Da

80.000 Ų

12

0

147.000

0

1

1.700

136054