20962-92-9 (N-烯丙基吩噻嗪,N-Allylphenothiazine)

CAS号:
20962-92-9
中文名称:
N-烯丙基吩噻嗪
英文名称:
N-Allylphenothiazine
分子式:
C15H13NS
分子量:
239.335422277451

N-烯丙基吩噻嗪(20962-92-9)名称与标识符

名称

中文别名:
N-烯丙基吩噻嗪;
英文别名:
N-Allylphenothiazine;10-prop-2-enylphenothiazine;10-(2-Propen-1-yl)-10H-phenothiazine (ACI);10H-Phenothiazine, 10-(2-propenyl)- (9CI);Phenothiazine, 10-allyl- (6CI, 8CI);10-Allyl-10H-phenothiazine;10-Allylphenothiazine;

标识符

InChIKey:
GFVSLJXVNAYUJE-UHFFFAOYSA-N
Inchi:
1S/C15H13NS/c1-2-11-16-12-7-3-5-9-14(12)17-15-10-6-4-8-13(15)16/h2-10H,1,11H2
SMILES:
S1C2C(=CC=CC=2)N(CC=C)C2C1=CC=CC=2

N-烯丙基吩噻嗪(20962-92-9)物化性质

实验特性

  • PSA : 3.24

计算特性

  • 精确分子量 : 239.07699

N-烯丙基吩噻嗪(20962-92-9)推荐厂家 更多厂家(5)

公司名称手机号/电话联系人QQ微信询单
上海楷森生物科技有限公司 17558870519
175-58870519
赵经理 3003926540
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西安德而塔生物科技有限公司 18133906270
18133906270
张女士 2590956145
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西安德而塔生物科技有限公司 18133906270
18133906270
张女士 2590956145
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深圳振强生物技术有限公司 13670046396
86-755-66853366
颜经理 2851296953
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上海绩祥生物科技有限公司 13093077543陆经理 3985448220
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N-烯丙基吩噻嗪(20962-92-9)合成路线

合成路线:1 步
反应条件:
参考文献:
Phenanthroimidazole/carbazole and phenanthroimidazole/phenothiazine hybrids with alkoxyorganosilane functional groups as blue emitting materials
Zhang, Chen; Su, Ruige; Guo, Yongchun; Li, Debao; Zhao, Jiaqin; et al, Journal of Molecular Structure, 2022, 1262,
合成路线:1 步
反应条件:
参考文献:
Sugar-urea-salt eutectic mixture as an efficient green solvent for N-alkylation of heterocyclic secondary amines
Kumar, Koravangala S. Vinay; Swaroop, Toreshettahally R.; Ravi Singh, Krishna; Rangappa, Kanchugarakoppal S.; Sadashiva, Maralinganadoddi P., Chemical Data Collections, 2020, 29,
合成路线:1 步
反应条件:
参考文献:
A Novel N-Benzylation of Phenothiazine with Benzyl Alcohols Activated by n-Propylphosphonic Acid Anhydride (T3P)
Levi, Lucilla; Scheuren, Sven; Mueller, Thomas J. J., Synthesis, 2014, 46(22), 3059-3066
合成路线:1 步
反应条件:
参考文献:
Simple palladium-catalyzed C-N bond formation for poor nucleophilicity of aminonaphthalenes
Shue, Yi-Jen; Yang, Shyh-Chyun, Applied Organometallic Chemistry, 2011, 25(12), 883-890
合成路线:1 步
反应条件:
参考文献:
Walking on the surface of phenothiazines: a combined experimental and theoretical approach
Porumb, Dan; Lovasz, Tamas; Rachita, Gratiana; Cristea, Castelia; Gaina, Luiza; et al, Revue Roumaine de Chimie, 2010, 55(11-12), 879-884
合成路线:1 步
反应条件:
参考文献:
Platinum-catalyzed allylation of aminonaphthalenes with allylic acetates in water
Gan, Kim-Hong; Jhong, Ciou-Jyu; Shue, Yi-Jen; Yang, Shyh-Chyun, Tetrahedron, 2008, 64(40), 9625-9629
合成路线:1 步
反应条件:
参考文献:
Platinum-catalyzed allylation of aminonaphthalenes with allylic acetates
Yang, Shyh-Chyun; Feng, Wei-Hao; Gan, Kim-Hong, Tetrahedron, 2006, 62(15), 3752-3760
合成路线:1 步
反应条件:
参考文献:
Palladium-catalyzed allylation of acidic and less nucleophilic anilines using allylic alcohols directly
Hsu, Yi-Chun; Gan, Kim-Hong; Yang, Shyh-Chyun, Chemical & Pharmaceutical Bulletin, 2005, 53(10), 1266-1269
合成路线:1 步
反应条件:
参考文献:
Monomeric and Polymeric Phenothiazine Photosensitizers for Photoinitiated Cationic Polymerization
Gomurashvili, Zaza; Crivello, James V., Macromolecules, 2002, 35(8), 2962-2969
合成路线:1 步
反应条件:
参考文献:
Alkylation of phenothiazine using solid-liquid phase-transfer catalysis without solvent
Vlassa, M.; Cenan, M., Revue Roumaine de Chimie, 1988, 33(2), 195-7