823-94-9 (2,4,6-trimethyl-1,3,5-triazine-2,4,6-三甲基-1,3,5-三嗪,2,4,6-trimethyl-1,3,5-triazine)

CAS号:
823-94-9
中文名称:
2,4,6-trimethyl-1,3,5-triazine-2,4,6-三甲基-1,3,5-三嗪
英文名称:
2,4,6-trimethyl-1,3,5-triazine
分子式:
C6H9N3
分子量:
123.155760526657

2,4,6-trimethyl-1,3,5-triazine-2,4,6-三甲基-1,3,5-三嗪(823-94-9)名称与标识符

名称

中文别名:
2,4,6-trimethyl-1,3,5-triazine-2,4,6-三甲基-1,3,5-三嗪;2,4,6-三甲基-1,3,5-三嗪;
英文别名:
2,4,6-trimethyl-1,3,5-triazine;1,3,5-Triazine, 2,4,6-trimethyl-;2,4,6-TRIMETHYL-S-TRIAZINE;s-Triazine, 2,4,6-trimethyl-;2,4,6-Trimethyl-1,3,5-triazine (ACI);s-Triazine, 2,4,6-trimethyl- (6CI, 7CI, 8CI);2,4,6-Trimethyl-1,3,5-s-triazine;Trimethyl-s-triazine;Trimethyltriazine;A12862;SCHEMBL92460;CS-0129379;AS-60791;Trimethyl-s-triazin;LASVAZQZFYZNPK-UHFFFAOYSA-N;2,4,6-trimethyl-[1,3,5]triazine;AI3-61023;DTXSID80231678;YSWG313;MFCD00456896;SY270782;trimethyl-1,3,5-triazine;SB73694;823-94-9;AKOS027324978;

标识符

MDL:
MFCD00456896
InChIKey:
LASVAZQZFYZNPK-UHFFFAOYSA-N
Inchi:
1S/C6H9N3/c1-4-7-5(2)9-6(3)8-4/h1-3H3
SMILES:
N1C(C)=NC(C)=NC=1C

2,4,6-trimethyl-1,3,5-triazine-2,4,6-三甲基-1,3,5-三嗪(823-94-9)物化性质

实验特性

  • 折射率 : 1.505
  • 沸点 : 289.3°C at 760 mmHg
  • 闪点 : 137°C
  • 密度 : 1.044

计算特性

  • 精确分子量 : 123.079647
  • 氢键供体数量 : 0
  • 氢键受体数量 : 0
  • 可旋转化学键数量 : 0
  • 同位素质量 : 123.079647
  • 重原子数量 : 9
  • 复杂度 : 63.3
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 1.2
  • 拓扑分子极性表面积 : 38.7

2,4,6-trimethyl-1,3,5-triazine-2,4,6-三甲基-1,3,5-三嗪(823-94-9)推荐厂家 更多厂家(24)

2,4,6-trimethyl-1,3,5-triazine-2,4,6-三甲基-1,3,5-三嗪(823-94-9)合成路线

合成路线:1 步
反应条件:
参考文献:
Mesoporous graphitic carbon nitride as a versatile, metal-free catalyst for the cyclisation of functional nitriles and alkynes
Goettmann, Frederic; et al, New Journal of Chemistry, 2007, 31(8), 1455-1460
合成路线:1 步
反应条件:
参考文献:
A practical and easy synthesis of 2,4,6-trisubstituted-s-triazines
Herrera, Antonio; et al, Synthesis, 2004, (4), 503-505
合成路线:1 步
反应条件:
参考文献:
Synthesis of octupolar molecule 2,4,6-tris[4-[4-[N-ethyl-N-(2-hydroxyethyl)] amino-phenylazo]styryl]-s-triazine
Yang, Fei; et al, Hecheng Huaxue, 2011, 19(2), 222-224
合成路线:1 步
反应条件:
参考文献:
A triazine-based multi-branched platinum acetylide complex: synthesis and photophysical properties
Guo, Jin; et al, Letters in Organic Chemistry, 2013, 10(1), 22-26
合成路线:1 步
反应条件:
参考文献:
Synthesis and characterization of novel blue light-conversion agents: 2-pentylene-4,6-bis((1-phenyl)-1, 3-butadiene)-1,3,5-s-triazine
Luo, Guilin; et al, Guizhou Shifan Daxue Xuebao, 2010, 28(3), 93-95
合成路线:1 步
反应条件:
参考文献:
Synthesis and characterization of novel blue light-conversion agent of triazine series in agricultural film
Luo, Gui-lin, Anhui Nongye Kexue, 2010, 38(29), 16090-16091
合成路线:1 步
反应条件:
参考文献:
Study on synthesis of s-triazine derivatives and their luminescence properties
Wang, Guang-rong, Huaxue Yanjiu Yu Yingyong, 2015, 27(7), 951-956
合成路线:1 步
反应条件:
参考文献:
Synthesis and characterisation of 2,6-di(2-hydroxy-styryl) 4-dimethyl-1,3,5-triazine
Zhou, Zi-yan; et al, Fenzi Kexue Xuebao, 2013, 29(3), 232-236
合成路线:1 步
反应条件:
参考文献:
Novel synthesis of olefin-linked covalent organic frameworks via aldol condensation
Chen, Jiansong; et al, Huagong Jinzhan, 2021, 40(12), 6765-6776
合成路线:1 步
反应条件:
参考文献:
Triazines. II. Trimethyltriazine
Grundmann, Christoph; et al, Chemische Berichte, 1951, 84, 684-8
合成路线:1 步
参考文献:
Synthesis of the s-triazine system. III. Trimerization of imidates
Schaefer, Fred C.; et al, Journal of Organic Chemistry, 1961, 26, 2778-84
合成路线:2 步
反应条件:
参考文献:
A triazine-based multi-branched platinum acetylide complex: synthesis and photophysical properties
Guo, Jin; et al, Letters in Organic Chemistry, 2013, 10(1), 22-26
合成路线:2 步
反应条件:
参考文献:
Synthesis, characterization and properties of a new octupolar molecule
Qi, Xiaoyun; et al, Hubei Daxue Xuebao, 2012, 34(2), 176-179
合成路线:1 步
反应条件:
参考文献:
Lanthanide(III) ion-catalyzed reaction of ammonia and nitriles. Synthesis of 2,4,6-trisubstituted-s-triazines
Forsberg, John H.; et al, Journal of Heterocyclic Chemistry, 1988, 25(3), 767-70
合成路线:1 步
反应条件:
参考文献:
Cyclotrimerization of nitriles by the reactive alkali metal hydrides
Zhang, Wen Ming; et al, Chinese Chemical Letters, 1995, 6(10), 839-42
合成路线:1 步
反应条件:
参考文献:
Formation of 1,2,4-triazoles by cation radical-induced oxidative addition of arylhydrazones of benzaldehyde and butyraldehyde to nitriles
Shine, Henry J.; et al, Journal of Organic Chemistry, 1988, 53(18), 4349-53
合成路线:1 步
反应条件:
参考文献:
Addition and substitution reactions of nitrile-stabilized carbanions
Arseniyadis, Simeon; et al, Organic Reactions (Hoboken, 1984, 31,
合成路线:1 步
反应条件:
参考文献:
Reaction of amidoximes with acetonitrile at high pressure
Baykov, Sergey V.; et al, Mendeleev Communications, 2016, 26(3), 264-265
合成路线:1 步
反应条件:
参考文献:
Reaction of amidoximes with acetonitrile at high pressure
Baykov, Sergey V.; et al, Mendeleev Communications, 2016, 26(3), 264-265
合成路线:1 步
反应条件:
参考文献:
Reaction of amidoximes with acetonitrile at high pressure
Baykov, Sergey V.; et al, Mendeleev Communications, 2016, 26(3), 264-265
合成路线:1 步
参考文献:
Product subclass 3: 1,3,5-triazines and phosphorus analogues
von Angerer, S., Science of Synthesis, 2004, 17, 449-583
合成路线:1 步
参考文献:
High-temperature transnitrilation of 2-bromocaproic acid
Polivin, Yu. N.; et al, Izvestiya Akademii Nauk SSSR, 1990, (7), 1682-4

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