88965-00-8 (6-甲基-2-(4-甲基苯基)咪唑[1,2-a]吡啶,6-methyl-2-(4-methylphenyl)imidazo1,2-apyridine)

CAS号:
88965-00-8
中文名称:
6-甲基-2-(4-甲基苯基)咪唑[1,2-a]吡啶
英文名称:
6-methyl-2-(4-methylphenyl)imidazo1,2-apyridine
分子式:
C15H14N2
分子量:
222.285063266754
API:

6-甲基-2-(4-甲基苯基)咪唑[1,2-a]吡啶(88965-00-8)名称与标识符

名称

中文别名:
6-甲基-2-(4-甲基苯基)咪唑[1,2-a]吡啶;6-甲基-2-对甲苯基吡啶并咪唑;6-甲基-2-对甲苯基咪唑[1,2-a]吡啶;
英文别名:
6-Methyl-2-(p-tolyl)imidazo[1,2-a]pyridine;2297527;6-Methyl-2-(4-methylphenyl)-imidazo[1,2-a]pyridine;6-Methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridine;6-methyl-2-(4-methylphenyl)imidazo[1,2-alpha]pyridine;6-METHYL-2-P-TOLY-IIDAZOLE(1,2)PYRIDINE;C15H14N2;6-Methyl-2-p-tolyl-imidazo[1,2-a]pyridine;2-(4-Methylphenyl)-6-methylimidazo[1,2-a]pyridine;6-Methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridine (ACI);6-methyl-2-(4-methylphenyl)imidazo1,2-apyridine;BAS 03308107;AWEWSJJCANQFRB-UHFFFAOYSA-N;SY109614;2-(4-methylphenyl)-6-methylimidazo[1,2-a]-pyridine;F0916-3171;6-methyl-2-p-tolylimidazo[1,2-a]pyridine;Z55863282;6-Methyl-2-(4-methylphenyl)-imidazo[1,2-a]-pyridine;CS-0172131;AC-6594;HMS2715J04;AKOS000527449;DS-18359;6-Methyl-2-(4-methylphenyl)imidazo [1,2-alpha]pyridine;Imidazo[1,2-a]pyridine, 6-methyl-2-(4-methylphenyl)-; 2-(4-Methylphenyl)-6-methylimidazo[1,2-a]pyridine;SMR000288756;CCG-239353;6-methyl-2-(4-methylphenyl)-4-hydroimidazo[1,2-a]pyridine;CHEMBL1440422;MLS000707291;SCHEMBL396368;BDBM50609283;DTXSID00349880;BRD-K71668435-001-10-7;STK702061;MFCD00444739;88965-00-8;AB05980;

标识符

MDL:
MFCD00444739
InChIKey:
AWEWSJJCANQFRB-UHFFFAOYSA-N
Inchi:
1S/C15H14N2/c1-11-3-6-13(7-4-11)14-10-17-9-12(2)5-8-15(17)16-14/h3-10H,1-2H3
SMILES:
N1=C2N(C=C(C)C=C2)C=C1C1C=CC(C)=CC=1

6-甲基-2-(4-甲基苯基)咪唑[1,2-a]吡啶(88965-00-8)物化性质

实验特性

  • LogP : 3.61810
  • PSA : 17.30000
  • 折射率 : 1.615
  • 颜色与性状 : White to Yellow Solid
  • 密度 : 1.09

计算特性

  • 精确分子量 : 222.11600
  • 氢键供体数量 : 0
  • 氢键受体数量 : 2
  • 可旋转化学键数量 : 1
  • 同位素质量 : 222.116
  • 重原子数量 : 17
  • 复杂度 : 258
  • 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) : 4.2
  • 拓扑分子极性表面积 : 17.3A^2

6-甲基-2-(4-甲基苯基)咪唑[1,2-a]吡啶(88965-00-8)安全信息

6-甲基-2-(4-甲基苯基)咪唑[1,2-a]吡啶(88965-00-8)海关数据

海关编码:
2933990090
海关数据:

中国海关编码:

2933990090

概述:

2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

申报要素:

品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期

Summary:

2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

6-甲基-2-(4-甲基苯基)咪唑[1,2-a]吡啶(88965-00-8)推荐厂家 更多厂家(52)

6-甲基-2-(4-甲基苯基)咪唑[1,2-a]吡啶(88965-00-8)合成路线

合成路线:1 步
反应条件:
参考文献:
Microwave-assisted synthesis of Imidazo[1,2-a]pyridine derivatives and their anti-inflammatory activity
Budumuru, Pushpalatha; Golagani, Srinivasarao; Pushpanjali, B., International Journal of Pharmaceutical Sciences and Research, 2019, 10(3), 1172-1179
合成路线:1 步
反应条件:
参考文献:
A simple, efficient and scalable synthesis of hypnotic agent, zolpidem
Sumalatha, Yasareni; Reddy, Tamma Ranga; Reddy, Padi Pratap; Satyanarayana, Bollikonda, ARKIVOC (Gainesville, 2008, (2), 315-320
合成路线:1 步
反应条件:
参考文献:
Copper(I) Iodide Catalyzed Aerobic Oxidative C-N and C-S bond formations through C-H Activation: Synthesis of Functionalized Imidazo[1,2-a]pyridines
Mohan, Darapaneni Chandra; Rao, Sadu Nageswara; Ravi, Chitrakar; Adimurthy, Subbarayappa, Asian Journal of Organic Chemistry, 2014, 3(5), 609-613
合成路线:1 步
反应条件:
参考文献:
Synthesis and Structure-Activity Relationships of Imidazopyridine/Pyrimidine- and Furopyridine-Based Anti-infective Agents against Trypanosomiases
Silva, Daniel G. ; Junker, Anna ; de Melo, Shaiani M. G.; Fumagalli, Fernando ; Gillespie, J. Robert ; et al, ChemMedChem, 2021, 16(6), 966-975
合成路线:1 步
反应条件:
参考文献:
Formation of Methylene Linkage for N-Heterocycles: Sequential C-H and C-O Bond Functionalization of Methanol with Cosolvent Water
Li, Na; Bai, Jinku; Zheng, Xiaolin; Rao, Honghua, Journal of Organic Chemistry, 2019, 84(11), 6928-6939
合成路线:1 步
反应条件:
参考文献:
Iodide-Catalyzed Phosphorothiolation of Heteroarenes Using P(O)H Compounds and Elemental Sulfur
Shi, Shanshan; Chen, Jun; Zhuo, Shaohua; Wu, Zi'ang; Fang, Meijuan; et al, Advanced Synthesis & Catalysis, 2019, 361(13), 3210-3216
合成路线:1 步
反应条件:
参考文献:
Iron-Catalyzed Dehydrogenative sp3-sp2 Coupling via Direct Oxidative C-H Activation of Acetonitrile
Su, Huimin; Wang, Luyao; Rao, Honghua ; Xu, Hao, Organic Letters, 2017, 19(9), 2226-2229
合成路线:1 步
反应条件:
参考文献:
Efficient and green microwave-assisted one-pot synthesis of azaindolizines in PEG-400 and water
Wagare, Devendra S.; Farooqui, Mazhar; Keche, Tushar D.; Durrani, Ayesha, Synthetic Communications, 2016, 46(21), 1741-1746
合成路线:1 步
反应条件:
参考文献:
Iodine Promoted Efficient Synthesis of 2-Arylimidazo[1,2-a]pyridines in Aqueous Media: A Comparative Study between Micellar Catalysis and an "On-Water" Platform
Bhutia, Zigmee T.; Panjikar, Padmini C.; Iyer, Shruti; Chatterjee, Amrita ; Banerjee, Mainak, ACS Omega, 2020, 5(22), 13333-13343
合成路线:1 步
反应条件:
参考文献:
Ag(I)-Promoted Decarboxylative Annulation of Alkynoic Acids towards 2-Arylimidazo[1,2-a]pyridines
Liu, Yun ; Wang, Ziqing; Lei, Ting; Li, Yuling, ChemistrySelect, 2022, 7(47),
合成路线:1 步
反应条件:
参考文献:
CuI-Catalyzed Aerobic Oxidative α-Amination Cyclization of Ketones to Access Aryl or Alkenyl-Substituted Imidazoheterocycles
Zhang, Yuanfei; Chen, Zhengkai; Wu, Wenliang; Zhang, Yuhong; Su, Weiping, Journal of Organic Chemistry, 2013, 78(24), 12494-12504
合成路线:1 步
反应条件:
参考文献:
Aqueous phase synthesis of substituted imidazo[1,2-a]pyridine in the presence of β-cyclodextrin
Kumbhar, Vijay V.; Hangirgekar, Shankar P.; Wadwale, Navanand B., Pharma Chemica, 2013, 5(5), 274-279
合成路线:1 步
反应条件:
参考文献:
Copper catalyzed tandem oxidative C-H amination/cyclizations: Direct access to imidazo[1,2-a]pyridines
Pericherla, Kasiviswanadharaju; Kaswan, Pinku; Khedar, Poonam; Khungar, Bharti; Parang, Keykavous; et al, RSC Advances, 2013, 3(41), 18923-18930
合成路线:1 步
反应条件:
参考文献:
Rhodium(II)-Catalyzed Regioselective C3-Alkylation of 2-Arylimidazo[1,2-a]pyridines with Aryl Diazoesters
Kim, Hyunseok; Byeon, Minhyeon; Jeong, Eunchong; Baek, Yonghyeon; Jeong, Seung Jin; et al, Advanced Synthesis & Catalysis, 2019, 361(9), 2094-2106
合成路线:1 步
参考文献:
Synthesis and antiproliferative activity evaluation of steroidal imidazo[1,2-a]pyridines
Rassokhina, Irina V.; Volkova, Yulia A.; Kozlov, Andrey S.; Scherbakov, Alexander M.; Andreeva, Olga E.; et al, Steroids, 2016, 113, 29-37
合成路线:1 步
反应条件:
参考文献:
Solvent-dependence of KI Mediated Electrosynthesis of Imidazo[1,2-a]pyridines
Yi, Yangjie; Xu, Leitao; Liu, Yuyang; Li, Mingfang; Zhang, Lijuan; et al, Chemical Research in Chinese Universities, 2023, 39(2), 318-324
合成路线:1 步
反应条件:
参考文献:
Multicomponent Synthesis of Imidazo[1,2-a]pyridines: Aerobic Oxidative Formation of C-N and C-S Bonds by Flavin-Iodine-Coupled Organocatalysis
Okai, Hayaki; Tanimoto, Kazumasa; Ohkado, Ryoma; Iida, Hiroki, Organic Letters, 2020, 22(20), 8002-8006

6-甲基-2-(4-甲基苯基)咪唑[1,2-a]吡啶(88965-00-8)上下游