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2-苯基咪唑啉 | 936-49-2

2-苯基咪唑啉
2-Phenyl-2-imidazoline
936-49-2
C9H10N2
146.189101696014
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:2-苯基咪唑啉结构式
13639
2-苯基咪唑啉价格
名称和标识符
MDL MFCD00005180
InChIKey BKCCAYLNRIRKDJ-UHFFFAOYSA-N
Inchi 1S/C9H10N2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-5H,6-7H2,(H,10,11)
SMILES N1CCNC=1C1C=CC=CC=1
别名信息
- 中文别名 -
  • 2-苯基咪唑啉
  • 2-苯基-2-咪唑啉
  • 2-苯基-4,5-二氢-1H-咪唑
  • 2-苯基-4,5-二氢化咪唑
- 英文别名 -
  • 2-Phenyl-4,5-dihydro-1H-imidazole
  • 2-Phenylimidazoline
  • 2-Phenyl-2-imidazoline
  • 4,5-Dihydro-2-phenyl-1H-imidazole
  • 2-Imidazoline,2-phenyl- (6CI,7CI,8CI)
  • 2-Phenyl-4,5-dihydroimidazole
  • 2PZ-L
  • B 31
  • Curezol2PZ-L
  • NSC 54747
  • Veba B 31
  • Vestagon B 31
  • 2-Imidazoline, 2-phenyl- (6CI, 7CI, 8CI)
  • 4,5-Dihydro-2-phenyl-1H-imidazole (ACI)
  • Curezol 2PZ-L
  • Curezol 2PZL-T
  • Eutomer B 31
  • Jietongda SA 31
  • SA 31
物化性质
实验特性
LogP 0.80080
PSA 24.39000
折射率 1.5600 (estimate)
水溶性 溶解
沸点 181°C/20mmHg(lit.)
熔点 100.0 to 103.0 deg-C
闪点 华氏:303.8 °F
摄氏:151 °C
颜色与性状 白色结晶
溶解性 未确定
最大波长(λmax) 325(lit.)
密度 1,15 g/cm3
计算特性
精确分子量 146.08400
氢键供体数量 1
氢键受体数量 2
可旋转化学键数量 1
同位素质量 146.084
重原子数量 11
复杂度 157
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) 0.9
互变异构体数量
表面电荷 0
拓扑分子极性表面积 24.4A^2
国际标准相关数据
EINECS 213-313-4
海关数据
海关编码 2933290090
海关数据

中国海关编码:

2933290090

概述:

2933290090. 其他结构含非稠合咪唑环的化合物. 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:

2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

合成路线

合成路线:1 步

反应条件:
参考文献:
An efficient preparation of 2-imidazolines and imidazoles from aldehydes with molecular iodine and (diacetoxyiodo)benzene
Ishihara, Midori; Togo, Hideo, Synlett, 2006, (2), 227-230

合成路线:1 步

反应条件:
参考文献:
Metal-free one-pot synthesis of 1,3-diazaheterocyclic compounds via I2-mediated oxidative C-N bond formation
Tian, Xianhai; Song, Lina; Li, Ertong; Wang, Qiang; Yu, Wenquan; et al, RSC Advances, 2015, 5(76), 62194-62201

合成路线:1 步

反应条件:
参考文献:
Synthesis of benzimidazole and quinoxaline derivatives using reusable sulfonated rice husk ash (RHA-SO3H) as a green and efficient solid acid catalyst
Shamsi-Sani, Mahnaz; Shirini, Farhad; Abedini, Masoumeh; Seddighi, Mohadeseh, Research on Chemical Intermediates, 2016, 42(2), 1091-1099

合成路线:1 步

反应条件:
参考文献:
Green and rapid and instrumental one-pot method for the synthesis of imidazolines having potential anti-SARS-CoV-2 main protease activity
Azimi, Sabikeh; Merza, Muna S.; Ghasemi, Fatemeh; Dhahi, Hasan Ali; Baradarbarjastehbaf, Farid; et al, Sustainable Chemistry and Pharmacy, 2023, 34,

合成路线:1 步

反应条件:
参考文献:
Carbon-transfer reactions of Δ2-oxazolinium and -thiazolinium cations
Singh, Harjit; Sarin, Rakesh, Tetrahedron, 1986, 42(5), 1449-60

合成路线:1 步

反应条件:
参考文献:
Microwave-assisted cascade cycloaddition for C-N bond formation: an approach to the construction of 1,4,5,6-tetrahydropyrimidine and 2-imidazoline derivatives
An, Shujuan; Yin, Bing; Liu, Ping; Li, Xiangnan; Li, Chen; et al, Synthesis, 2013, 45(18), 2525-2532

合成路线:1 步

反应条件:
参考文献:
Preparation of cyclic amidines
, Germany, , ,

合成路线:1 步

反应条件:
参考文献:
One-pot synthesis of imidazolines from aldehydes: detailed study about solvents and substrates
Fujioka, Hiromichi; Murai, Kenichi; Kubo, Ozora; Ohba, Yusuke; Kita, Yasuyuki, Tetrahedron, 2007, 63(3), 638-643

合成路线:1 步

反应条件:
参考文献:
Microwave-assisted facile and convenient synthesis of imidazolines
Mohammadpoor-Baltork, I.; Abdollahi-Alibeik, M., Bulletin of the Korean Chemical Society, 2003, 24(9), 1354-1356

合成路线:1 步

反应条件:
参考文献:
Green Synthesis of 2-Substituted Imidazolines using Hydrogen Peroxide Catalyzed by Tungstophosphoric Acid and Tetrabutylammonium Bromide in Water
Liu, Shuai; Li, Wang; Pang, Yiying; Xiao, Hesheng; Zhou, Yi; et al, Journal of Heterocyclic Chemistry, 2019, 56(3), 998-1002

合成路线:1 步

反应条件:
参考文献:
Synthesis of novel C-2 substituted imidazoline derivatives having the norbornene/dibenzobarrelene skeletons
Capan, Irfan; Servi, Suleyman, ARKIVOC (Gainesville, 2018, (7), 131-142

合成路线:1 步

反应条件:
参考文献:
A facile and efficient synthesis of 2-imidazolines from aldehydes using hydrogen peroxide and substoichiometric sodium iodide
Bai, Guo-yi; Xu, Kai; Chen, Guo-feng; Yang, Yong-hui; Li, Tian-yu, Synthesis, 2011, (10), 1599-1603

合成路线:1 步

反应条件:
参考文献:
Solvent-free and water-mediated synthesis of 2-substituted imidazolines using iron(III) phosphate
Behbahani, Farahnaz K.; Daloee, Toktam Sheibani; Ziaei, Parisa, Current Organic Chemistry, 2013, 17(3), 296-303

合成路线:1 步

反应条件:
参考文献:
Palladium-Catalyzed Multicomponent Synthesis of 2-Aryl-2-imidazolines from Aryl Halides and Diamines
Geden, Joanna V.; Pancholi, Alpa K.; Shipman, Michael, Journal of Organic Chemistry, 2013, 78(8), 4158-4164

合成路线:1 步

反应条件:
参考文献:
Facile preparation of 2-imidazolines from aldehydes with tert-butyl hypochlorite
Ishihara, Midori; Togo, Hideo, Synthesis, 2007, (13), 1939-1942

合成路线:1 步

反应条件:
参考文献:
Direct oxidative conversion of aldehydes and alcohols to 2-imidazolines and 2-oxazolines using molecular iodine
Ishihara, Midori; Togo, Hideo, Tetrahedron, 2007, 63(6), 1474-1480

合成路线:1 步

反应条件:
参考文献:
A mild and efficient one-pot synthesis of 2-dihydroimidazoles from aldehydes
Fujioka, Hiromichi; Murai, Kenichi; Ohba, Yusuke; Hiramatsu, Atsushi; Kita, Yasuyuki, Tetrahedron Letters, 2005, 46(13), 2197-2199

合成路线:1 步

反应条件:
参考文献:
Synthesis and acaricidal activity of 1-arylmethyl-2-arylimidazolidines
Kagabu, Shinzo; Sakou, Misa; Iwaya, Kazuko; Kiriyama, Kazuhisa, Nippon Noyaku Gakkaishi, 2001, 26(4), 393-398

合成路线:1 步

反应条件:
参考文献:
Rapid and efficient synthesis of imidazolines and bisimidazolines under microwave and ultrasonic irradiation
Moghadam, Majid; Mohammadpoor-Baltork, Iraj; Mirkhani, Valiollah; Tangestaninejad, Shahram; Abdollahi-Alibeik, Mohammad; et al, Monatshefte fuer Chemie, 2007, 138(6), 579-583

合成路线:1 步

反应条件:
参考文献:
Palladium(0)-catalyzed, copper(I)-mediated coupling of boronic acids with cyclic thioamides. selective carbon-carbon bond formation for the functionalization of heterocycles
Prokopcova, Hana; Kappe, C. Oliver, Journal of Organic Chemistry, 2007, 72(12), 4440-4448
相关文献
专业数据库参考
PubChemId 13639
参考资料
Reaxys RN 119250
Beilstein 23,154
化合物详情(旧版)

SMILES

C1=CC=C(C=C1)C2=NCCN2

产品用途
可作为环氧树脂粉末涂层的固化剂
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