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N'-tert-butylnaphthalene-1-carbohydrazide | 112225-94-2

中文名称
——
中文别名
——
英文名称
N'-tert-butylnaphthalene-1-carbohydrazide
英文别名
——
N'-tert-butylnaphthalene-1-carbohydrazide化学式
CAS
112225-94-2
化学式
C15H18N2O
mdl
——
分子量
242.321
InChiKey
KUQYBSIBTYKZFP-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

物化性质

  • 沸点:
    357.1±15.0 °C(predicted)
  • 密度:
    1.090±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.6
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    41.1
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    5-methyl-1,2,3-thiadiazole-4-carbonyl chlorideN'-tert-butylnaphthalene-1-carbohydrazide三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 7.0h, 以38%的产率得到
    参考文献:
    名称:
    Synthesis and bioactivity of N-tert-butyl-N′-acyl-5-methyl-1,2,3-thiadiazole-4-carbohydrazides
    摘要:
    A series of novel N-tert-butyl-N'-acyl-5-methyl-1,2,3-thiadiazole-4-carbohyclrazides were designed and synthesized. Their structures were characterized by melting points, H-1 NMR, IR, ESI-MS, and elemental analysis. The bioassay tests indicated that compound 7o exhibited excellent direct anti-TMV activity and induction activity in viva at 50 mu g/mL, which was better than that of Ninamycin and tiadinial. Our studies indicated that 1,2,3-thiadiazole was an active substructure for novel pesticide development. (C) 2012 Zhi Jin Fan. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
    DOI:
    10.1016/j.cclet.2012.09.024
  • 作为产物:
    描述:
    1-萘甲酸氯化亚砜 、 sodium hydroxide 作用下, 以 二氯甲烷 为溶剂, 反应 10.0h, 生成 N'-tert-butylnaphthalene-1-carbohydrazide
    参考文献:
    名称:
    Synthesis and bioactivity of N-tert-butyl-N′-acyl-5-methyl-1,2,3-thiadiazole-4-carbohydrazides
    摘要:
    A series of novel N-tert-butyl-N'-acyl-5-methyl-1,2,3-thiadiazole-4-carbohyclrazides were designed and synthesized. Their structures were characterized by melting points, H-1 NMR, IR, ESI-MS, and elemental analysis. The bioassay tests indicated that compound 7o exhibited excellent direct anti-TMV activity and induction activity in viva at 50 mu g/mL, which was better than that of Ninamycin and tiadinial. Our studies indicated that 1,2,3-thiadiazole was an active substructure for novel pesticide development. (C) 2012 Zhi Jin Fan. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
    DOI:
    10.1016/j.cclet.2012.09.024
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文献信息

  • RUBBER COMPOSITION AND PNEUMATIC TIRES
    申请人:Bridgestone Corporation
    公开号:EP0909788A1
    公开(公告)日:1999-04-21
    A rubber composition prepared by compounding 0.05 to 20 parts by weight of at least one selected from substituted hydrazide compounds represented by the following Formulas (I) to (IV) per 100 parts by weight of a rubber component comprising at least one rubber selected from the group consisting of natural rubber and synthetic rubber, and a pneumatic tire using the same: wherein A represents one selected from the group consisting of an aromatic group which may have a substituent, a hydantoin ring which may have a substituent, and a saturated or unsaturated linear hydrocarbon having 1 to 18 carbon atoms; Y represents hydrogen, an amino group, an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an alkenyl group, an aromatic group, a pyridyl group or hydrazino group; and R1 to R11 each represent hydrogen, an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group or an aromatic group.
    一种橡胶组合物,其制备方法是每 100 重量份由至少一种选自天然橡胶和合成橡胶组的橡胶组成的橡胶组分中混入 0.05 至 20 重量份的至少一种选自下式(I)至(IV)所代表的取代酰化合物,以及使用该组合物的充气轮胎: 其中 A 代表选自芳香基团(可具有取代基)、海因环(可具有取代基)和具有 1 至 18 个碳原子的饱和或不饱和线性烃;Y 代表氢、基、具有 1 至 18 个碳原子的烷基、环烷基、烯基、芳香基、吡啶基或基;R1 至 R11 分别代表氢、具有 1 至 18 个碳原子的烷基、环烷基或芳香基。
  • Rubber composition and pneumatic tire
    申请人:Bridgestone Corporation
    公开号:EP1420044A2
    公开(公告)日:2004-05-19
    A hydrazone derivative represented by Formula (V):         ZC(=O)NHN=C(CH3) (CH2CH(CH3)2)     (V) wherein Z represents 3-hydroxy-2-naphthyl, 1-hydroxy-2-naphthyl, 2-hydroxyphenyl or 2,6-dihydroxyphenyl group.
    式 (V) 所代表的腙衍生物: ZC(=O)NHN=C(CH3) (CH2CH( )2) (V) 其中 Z 代表 3-羟基-2-基、1-羟基-2-基、2-羟基苯基或 2,6-二羟基苯基。
  • US6380288B1
    申请人:——
    公开号:US6380288B1
    公开(公告)日:2002-04-30
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