549126
Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylate
97%
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About This Item
Empirical Formula (Hill Notation):
C6H8N2O2S
CAS Number:
Molecular Weight:
172.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylate, 97%
InChI
1S/C6H8N2O2S/c1-3-10-6(9)5-4(2)7-8-11-5/h3H2,1-2H3
SMILES string
CCOC(=O)c1snnc1C
InChI key
AHPXTXGCMLOXGA-UHFFFAOYSA-N
assay
97%
refractive index
n20/D 1.5050 (lit.)
density
1.265 g/mL at 25 °C (lit.)
functional group
ester
Application
Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylate may be used in the preparation of following compounds with potent fungicidal activity:
- 1,2,3-thiadiazole bearing hydrazone derivatives
- 2-(4′-methyl-1′,2′,3′-thiadiazol)-5-substituted-1,3,4-oxadiazole derivatives
- 1,2,3-thiadiazole bearing 1,2,4-triazole derivatives
General description
Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylate is a bioactive nitrogen-containing heterocycle.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Microwave assisted synthesis, antifungal activity and DFT theoretical study of some novel 1, 2, 4-triazole derivatives containing the 1, 2, 3-thiadiazole moiety.
Sun NB, et al.
Molecules (Basel), 18(10), 12725-12739 (2013)
Zhijin Fan et al.
Journal of agricultural and food chemistry, 57(10), 4279-4286 (2009-05-27)
Elicitors provide a broad spectrum of systemic acquired resistance by altering the physical and physiological status of the host plants and, therefore, are among the most successful directions in modern pesticide development for plant protection. To develop a novel elicitor
Microwave synthesis and biological activity of hydrazone derivatives containing 1, 2, 3-thiadiazole.
Liu XH, et al.
Asian Journal of Chemistry, 23(9), 4064-4064 (2011)
Synthesis of tetrazole containing 1, 2, 3-thiadiazole derivatives via U-4CR and their anti-TMV activity.
Wang SX, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 24(10), 889-892 (2013)
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