524409
2-Amino-5-tert-butyl-1,3,4-thiadiazole
97%
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About This Item
Empirical Formula (Hill Notation):
C6H11N3S
CAS Number:
Molecular Weight:
157.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
254-364-2
MDL number:
Product Name
2-Amino-5-tert-butyl-1,3,4-thiadiazole, 97%
InChI key
ICXDPEFCLDSXLI-UHFFFAOYSA-N
InChI
1S/C6H11N3S/c1-6(2,3)4-8-9-5(7)10-4/h1-3H3,(H2,7,9)
SMILES string
CC(C)(C)c1nnc(N)s1
assay
97%
mp
183-187 °C (lit.)
Application
2-Amino-5-tert-butyl-1,3,4-thiadiazole may be employed for the preparation of:
- 9H -2,6-di-tert -butyl-9-(2-hydroxyphenyl)-bis(1,3,4-thia-diazolo)[3,2-a:3",2"-d]-1,3,5-triazin-8-ium chloride
- 1,1-dimethyl-3-(5-tert-butyl-1,3,4-thiadiazol-2-yl)urea
- N-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-2,4-dihydroxythiobenzamide
General description
2-Amino-5-tert-butyl-1,3,4-thiadiazole (ABTD) is a thiadiazole derivative. It inhibits the corrosion of brass in sea water samples.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Jan Legocki et al.
Journal of agricultural and food chemistry, 51(2), 362-368 (2003-01-09)
Twenty-six compounds, derivatives of amides, hydrazines, hydrazides, hydrazones, and semicarbazides, with a 2,4-dihydroxythiobenzoyl moiety, were synthesized from sulfinyl-bis(2,4-dihydroxythiobenzoyl). The compositions and chemical structures of these compounds were confirmed by IR, (1)H NMR, EI-MS, and elemental analysis. Antifungal properties of chemicals
Corrosion inhibition effect of substituted thiadiazoles on brass.
Raj XJ and Rajendran N.
International Journal of Electrochemical Science, 6(2), 348-366 (2011)
Bis (1, 3, 4-Thiadiazolo)-1, 3, 5-Triazinium Halides 3; Synthesis of Guanidyl-Functionalized 1, 4, 8, 11-Tetraazacyclotetradecanes and Tris (2-amino-ethyl) amines: Application of a Novel Rearrangement.
Walther M, et al.
Synthesis, 2001(09), 1327-1330 (2001)
Herbicidal activity of 1, 3, 4-thiadiazole derivatives.
Kubo H, et al.
Journal of Agricultural and Food Chemistry, 18(1), 60-65 (1970)
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