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Merck
CN

549126

4-甲基-1,2,3-噻重氮-5-羧酸乙酯

97%

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关于此项目

经验公式(希尔记法):
C6H8N2O2S
化学文摘社编号:
分子量:
172.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
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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

General description

Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylate is a bioactive nitrogen-containing heterocycle.

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

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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)
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)

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