CAS: 13984-07-1; N-Methyl-N-(5-(Methyl(Phenyl)Amino)Penta-2,4-Dien-1-Ylidene)Benzenaminium Chloride

该化合物是一个化学化合物,其结构复杂,包括一个以甲基组和五环基碘酸盐替代的核核心.该化合物在苯氮基组中具有积极充电的氮原子特征,当与氯化物配对为对时,该化合物会助长其离子性质.甲基苯基氨组的存在表明,有可能发生重大的芳香相互作用,从而影响其溶性和再活性.五氯基甲烷结构表明,该化合物有可能影响分子的电子特性,有可能使其在各种应用中有用,包括有机合成和材料科学中.其氯化形式表明,它可能在极地溶剂中具有溶解性,而其电离子特性在生物系统中的行为中或化学反应中的再试剂中发挥作用.

英文名称N-Methyl-N-(5-(Methyl(Phenyl)Amino)Penta-2,4-Dien-1-Ylidene)Benzenaminium Chloride
中文名称甲基-(5-[N-甲基-N-苯基氨基]-2,4-戊二烯亚基)-苯基氯化铵
IUPAC名称N-methyl-N-((2E,4E)-5-(methyl(phenyl)amino)penta-2,4-dien-1-ylidene)benzenaminium chloride
其它别名Methyl-(5-[n-Methyl-N-Phenylamino]-2,4-Pentadienylidene)-Phenylammonium Chloride; N-Methyl-N-(5-(N’-Methylanilino)-2,4-Pentadienylidene)-Aniliniuchloride; N-Methyl-N-(5-(N’-Methylanilino)-2,4-Pentadienylidene)Aniliniumchloride; Methyl(5-(N-Methyl-N-Phenylamino)-2,4-Pen-Tadieny; N-Methyl-N-[5-(Benzylamino)Penta-2,4-Dienylidene]Aniline Hydrochloride; Methyl-5-N-Methyl-N-Phenylamino-2-4-*pen Tadienylide; Methyl-(5-[n-Methyl-N-Phenylamino]-2,4-Pentadienylidene)-Phenyl-Ammoniumchloridedyecontent:Approx; Methyl[5-(N-Methyl-N-Phenylamino)-2,4-Pentadienylidene]Phe
CAS编号13984-07-1
EINECS号:237-774-6
分子式:C19H21ClN2分子量:312.84
产品CID: 617154
产品分类化学试剂 → 有机试剂 → 亚氨,脒

相似结构搜索
InChIKey: FPYATAHHYUQBFA-UHFFFAOYSA-M
InChI=1S/C19H21N2.ClH/c1-20(18-12-6-3-7-13-18)16-10-5-11-17-21(2)19-14-8-4-9-15-19;/h3-17H,1-2H3;1H/q+1;/p-1
计算化学: 氢键受体数2.0氢键供体数0.0可旋转键数5.0

MSDS等安全信息

GHS象形图
GHS符号GHS07;
注释: Exclamation mark
危险类别急性毒性类别4(吸入)
急性毒性类别4(经皮)
急性毒性类别4(经口)
特定目标器官毒性 - 单次接触类别3
皮肤腐蚀/刺激类别2
严重眼刺激类别2
警示词Warning(警告)
危险描述H332 |吸入有害.
H312 |皮肤接触有害.
H302 |吞咽有害.
H335 |可能引起呼吸道刺激.
H315 |造成皮肤刺激.
H319 |造成严重眼刺激.
防范说明P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
UN编号UN 2811
危险品标志Xn
安全声明S26,S36
危险类别码R20/21/22,R36/37/38
WGK Germany3

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

1-(2,4-dinitrophenyl)-pyridinium chloride N-methylaniline 1,3,5,5-tetraethoxy-pent-1-ene-3-ethyl-1-phenylbenzimidazolium iodide5-Ethoxycarbonyl-2-7-(5-ethoxycarbonyl-3-ethyl-1-phenylbenzimidazol-2-ylidene)hepta-1,3,5-trien-1-yl-3-ethyl-1-phenylbenzimidazolium iodide N-methyl-anilino)-penta-2,4-dienal5-(N-methyl-anilino)-penta-2,4-dienal -3H-indol-3-on1,2-Dihydro-2-5'-(N-methylanilino)-2',4'-pentadienyliden-3H-indol-3-on -3H-pyrrol-3-on1,2-Dihydro-5-methyl-2-5'-(N-methylanilino)-2',4'-pentadienyliden-3H-pyrrol-3-on

合成工艺路线路线简述

📜1,3,5,5-Tetraethoxy-Pent-1-Ene,N-甲基苯胺置于盐酸体系中,化学反应生成甲基-(5-[n-甲基-N-苯基氨基]-2,4-戊二烯亚基)-苯基氯化铵
参考文献:Makin,S.M. Et Al.,Journal Of Organic Chemistry Ussr (English Translation),1970,Vol. 6,P. 455-459
标题:Makin,S.M. Et Al.,Journal Of Organic Chemistry Ussr (English Translation),1970,Vol. 6,P. 455-459