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1-phenyl-2-(propenyloamino)ethanone | 112698-35-8

中文名称
——
中文别名
——
英文名称
1-phenyl-2-(propenyloamino)ethanone
英文别名
1-Phenyl-2-(prop-2-enylamino)ethanone
1-phenyl-2-(propenyloamino)ethanone化学式
CAS
112698-35-8
化学式
C11H13NO
mdl
——
分子量
175.23
InChiKey
SEPVLIVEZCINQR-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    13
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1-phenyl-2-(propenyloamino)ethanonesodium hydroxide 作用下, 以 乙醇 为溶剂, 反应 1.33h, 生成 苯甲酸
    参考文献:
    名称:
    从物种中合成鸟嘌呤7氧化物(一种抗肿瘤抗生素)
    摘要:
    抗肿瘤抗生素鸟嘌呤7-氧化物(VI)的首次合成是通过4步路线实现的,该路线从苯甲酰溴(I)和硝基嘧啶酮III开始,并通过中间体IVe和Ve进行。
    DOI:
    10.1016/s0040-4039(00)95348-6
  • 作为产物:
    描述:
    参考文献:
    名称:
    从物种中合成鸟嘌呤7氧化物(一种抗肿瘤抗生素)
    摘要:
    抗肿瘤抗生素鸟嘌呤7-氧化物(VI)的首次合成是通过4步路线实现的,该路线从苯甲酰溴(I)和硝基嘧啶酮III开始,并通过中间体IVe和Ve进行。
    DOI:
    10.1016/s0040-4039(00)95348-6
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文献信息

  • Purines. L. Synthesis and Antileukemic Activity of the Antibiotic Guanine 7-Oxide and Its 9-Substituted Derivatives.
    作者:Kazuo OGAWA、Masahiro NISHII、Jin-ichiro INAGAKI、Fujio NOHARA、Tohru SAITO、Taisuke ITAYA、Tozo FUJII
    DOI:10.1248/cpb.40.343
    日期:——
    A full account is given of the first chemical synthesis of the antitumor antibiotic guanine 7-oxide (5) and its 9-substituted derivatives (24a--k and 26). Coupling of appropriate primary amines (17a--e, g--k) with phenacyl bromide (16) produced, after treatment with HCl, the corresponding N-substituted phenacylamine hydrochlorides (18a--e, g--k). A similar phenacylation of 4-amino-l-butanol (21) failed
    全面介绍了抗肿瘤抗生素鸟嘌呤7-氧化物(5)及其9-取代衍生物(24a-k和26)的首次化学合成。用HCl处理后,将适当的伯胺(17a-e,g-k)与苯甲酰溴(16)偶联,制得相应的N-取代的苯甲胺盐酸盐(18a-e,g-k)。4-氨基-1-丁醇(21)的类似苯甲酰化反应未能得到所需的化合物18f,因此将其与2-溴甲基-2-苯基-1,3-二氧戊环(20)在150-155摄氏度下加热在用HCl处理3小时后,提供缩酮盐酸盐22,产率为40%。用热的2 N HCl溶液对22进行缩酮化处理,得到18f,产率为96%。由盐酸盐18a-1和1N NaOH溶液原位生成的游离碱的缩合,用氯嘧啶酮6在沸点EtOH溶液中于沸点下进行20分钟或在25-30℃下进行3-24h,以54-90%的产率得到6-苯甲基-4-嘧啶酮19a-1。在室温下用2N NaOH溶液处理10-60分钟后,硝基嘧啶酮19a
  • Polymer coating compositions and coated products
    申请人:Ariste Medical, LLC
    公开号:US10314912B2
    公开(公告)日:2019-06-11
    Described herein are coating compositions for consumer and/or medical products. The coating compositions can be used to confer desirable properties to the consumer and/or medical products.
    本文描述了用于消费品和/或医疗产品的涂层组合物。这些涂层组合物可用于赋予消费品和/或医疗产品所需的性能。
  • Industrial Deinking of Ink Compositions
    申请人:Xeikon IP B.V.
    公开号:US20160177118A1
    公开(公告)日:2016-06-23
    The ink composition comprises pigment particles and a stimulus responsive dispersing agent for dispersing said pigment particles in a protic polar solvent, for instance for inkjet printing, which stimulus responsive dispersing agent comprises an anchoring part for anchoring to said pigment particles, a stimulus responsive part as shown in formula (XXa) or (XXb) and a hydrophilic part for solvent stabilization of the pigment, wherein the stimulus responsive part upon exposure to a stimulus initiates decomposition of the stimulus responsive dispersing agent. The paper with the printed ink can be deinked in an industrial deinking process.
    这段话的中文翻译如下: 墨组合物包括颜料粒子和一种刺激响应分散剂,用于在质子极性溶剂中分散颜料粒子,例如用于喷墨打印。该刺激响应分散剂包括用于锚定到颜料粒子的锚定部分,如公式(XXa)或(XXb)所示的刺激响应部分,以及用于溶剂稳定颜料的亲部分。当刺激响应部分暴露于刺激物时,会启动刺激响应分散剂的分解。印有该墨的纸张可以在工业脱墨过程中脱墨。
  • Dental adhesive kit
    申请人:SUN MEDICAL CO., LTD.
    公开号:EP0923924A2
    公开(公告)日:1999-06-23
    A kit for dental adhesive comprising a radical polymerizable monomer having an acid group in the molecule, a photosensitizer and/or a peroxide, a water-soluble organic solvent, an organic sulfinic acid and/or a salt thereof or a barbituric acid and/or a derivative thereof, and water. The kit may further comprises a radical polymerizable monomer which has no acid group and is insoluble or hardly soluble in water, an amine compound, a silane coupling agent and a 1,3,5-triazine-2,4-dithion derivative. By using this kit, the adhesive composition can be applied directly to a dentine without conducting a pretreatment.
    一种牙科粘合剂试剂盒,包括分子中含有酸基的可自由基聚合单体、光敏剂和/或过氧化物、溶性有机溶剂、有机亚硫酸和/或其盐或巴比妥酸和/或其衍生物以及。该试剂盒还可进一步包含不含酸基且不溶于或难溶于的自由基可聚合单体、胺化合物、硅烷偶联剂1,3,5-三嗪-2,4-二杂环衍生物。使用这种试剂盒,粘合剂组合物可以直接涂抹在牙本质上,而无需进行预处理。
  • DENTAL CURABLE COMPOSITION AND KIT FOR SUCH DENTAL CURABLE COMPOSITION
    申请人:SUN MEDICAL CO., LTD.
    公开号:EP1938781A1
    公开(公告)日:2008-07-02
    [Means for solution] A dental curable composition has a curing time of 30 seconds to 120 minutes and includes a compound having an acidic group in the molecule (A), a polymerizable monomer (B), an organic amine compound (C) and a sulfur-containing reducing compound (D). In the dental curable composition, the content of the component (A) is 0.01 to 80 parts by weight, the content of the component (B) is 21 to 99.8 parts by weight, the content of the component (C) is 0.01 to 30 parts by weight and the content of the component (D) is 0 to 30 parts by weight (the total of the components (A) to (D) is 100 parts by weight. When any of the compounds belongs to a plurality of the components (A) to (D), the parts by weight of the compound is divided by the number of the components to which the compound belongs, and the quotient is used as the content of each component). [Advantage] The composition may be cured at a relatively low temperature close to the body temperature without using a peroxide-based polymerization initiator, and has good sealing property and adhesion.
    [解决方法] 一种牙科固化组合物的固化时间为30秒至120分钟,包括分子中含有酸性基团的化合物(A)、可聚合单体(B)、有机胺化合物(C)和含还原化合物(D)。在牙科固化组合物中,组分(A)的含量为 0.01 至 80 份(按重量计),组分(B)的含量为 21 至 99.8 份(按重量计),组分(C)的含量为 0.01 至 30 份(按重量计),组分(D)的含量为 0 至 30 份(按重量计)(组分(A)至(D)的总和为 100 份(按重量计))。当任何一种化合物属于多种组分(A)至(D)时,该化合物的重量份数除以该化合物所属组分的数量,所得之商作为各组分的含量)。 优势 该组合物可在接近人体温度的相对低温下固化,无需使用过氧化物基聚合引发剂,并具有良好的密封性和粘合性。
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