方案
97%
mp
258-261 °C (lit.)
SMILES字符串
COc1nc(C)nc(N)n1
InChI
1S/C5H8N4O/c1-3-7-4(6)9-5(8-3)10-2/h1-2H3,(H2,6,7,8,9)
InChI key
NXFQWRWXEYTOTK-UHFFFAOYSA-N
一般描述
2-Amino-4-methoxy-6-methyl-1,3,5-triazine is formed during the photocatalytic decomposition of sulfonylurea (Sus) herbicide. It is also formed as a thermal decomposition product of chlorsulfuron (a sulfonylurea herbicide) and has been determined by GC using nitrogen-phosphorus detection (NPD).
应用
2-Amino-4-methoxy-6-methyl-1,3,5-triazine may be used in the synthesis of thifensulfuron.
警示用语:
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Photocatalytic degradation of sulfonylurea herbicides in aqueous TiO 2.
Vulliet E, et al.
Applied Catalysis. B, Environmental, 38(2), 127-137 (2002)
Analysis of sulfonylurea herbicides by gas-liquid chromatography. 1. Formation of thermostable derivatives of chlorsulfuron and metsulfuron-methyl.
Klaffenbach P and Holland PT.
Journal of Agricultural and Food Chemistry, 41(3), 388-395 (1993)
Synthesis of Thifensulfuron Using Bis (trichloromethyl) carbonate.
Yao RS, et al.
Chinese Journal of Applied Chemistry / Ying Yong Hua Xue, 19(7), 687-689 (2002)
Analysis of sulfonylurea herbicides by gas-liquid chromatography. 2. Determination of chlorsulfuron and metsulfuron-methyl in soil and water samples.
Klaffenbach P and Holland PT.
Journal of Agricultural and Food Chemistry, 41(3), 396-401 (1993)
Rajae Chahboune et al.
Rapid communications in mass spectrometry : RCM, 29(15), 1370-1380 (2015-07-07)
Sulfonylureas are among the most important class of antidiabetic and herbicides. Solar light excitation and Advanced Oxidation Processes may result in the formation of a wide array of products owing to the relative complex structure. These products, that should be
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