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Merck
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549126

Sigma-Aldrich

4-甲基-1,2,3-噻重氮-5-羧酸乙酯

97%

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About This Item

经验公式（希尔记法）:
C6H8N2O2S
CAS号:
18212-20-9
分子量:
172.20
MDL编号:
MFCD00052549
UNSPSC代码:
12352100
PubChem化学物质编号:
24879059
NACRES:
NA.22

方案

97%

折射率

n20/D 1.5050 (lit.)

密度

1.265 g/mL at 25 °C (lit.)

官能团

ester

SMILES字符串

CCOC(=O)c1snnc1C

InChI

1S/C6H8N2O2S/c1-3-10-6(9)5-4(2)7-8-11-5/h3H2,1-2H3

InChI key

AHPXTXGCMLOXGA-UHFFFAOYSA-N

一般描述

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

应用

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

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H319,H335

危险分类

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

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCP3386
16516AO

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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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