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1,7-萘二胺 | 2243-64-3

中文名称
1,7-萘二胺
中文别名
——
英文名称
1.7-Diamino-naphthalin
英文别名
1,7-Diaminonaphthalene;naphthalene-1,7-diamine
1,7-萘二胺化学式
CAS
2243-64-3
化学式
C10H10N2
mdl
——
分子量
158.203
InChiKey
ZDWYJINCYGEEJB-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:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    52
  • 氢给体数:
    2
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2921590090

SDS

SDS:39881905d7df6948bddc40ebb49b903b
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1,7-萘二胺盐酸 作用下, 生成 1,7-二氯-萘
    参考文献:
    名称:
    Friedlaender; Szymanski, Chemische Berichte, 1892, vol. 25, p. 2082
    摘要:
    DOI:
  • 作为产物:
    描述:
    7-nitro-1-naphthalenamine盐酸tin 作用下, 生成 1,7-萘二胺
    参考文献:
    名称:
    Schroeter et al., Chemische Berichte, 1930, vol. 63, p. 1308,1325
    摘要:
    DOI:
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文献信息

  • Nickel-Catalyzed Synthesis of Primary Aryl and Heteroaryl Amines via C–O Bond Cleavage
    作者:Huifeng Yue、Lin Guo、Xiangqian Liu、Magnus Rueping
    DOI:10.1021/acs.orglett.7b00556
    日期:2017.4.7
    A nickel-catalyzed protocol for the conversion of aryl and heteroaryl alcohol derivatives to primary and secondary aromatic amines via C(sp2)–O bond cleavage is described. The new amination protocol can be applied to a range of substrates bearing diverse functional groups and uses readily available benzophenone imines as an effective nitrogen source.
    描述了一种镍催化的方案,用于通过C(sp 2)-O键裂解将芳基和杂芳基醇衍生物转化为伯和仲芳族胺。新的胺化方案可应用于带有各种官能团的多种底物,并使用现成的二苯甲酮亚胺作为有效的氮源。
  • NOVEL DIAMINE, POLYAMIC ACID, AND POLYIMIDE
    申请人:NISSAN CHEMICAL INDUSTRIES. LTD.
    公开号:US20160264520A1
    公开(公告)日:2016-09-15
    To provide a novel diamine, and a polyimide precursor and a polyimide using it. A diamine represented by the formula (1): wherein each of X 1 and X 5 which are independent of each other, is a single bond or the like; each of X 2 and X 4 which are independent of each other, is —CH 2 — or the like; X 3 is a C 1-6 alkylene or the like; each of Y 1 and Y 2 which are independent of each other, is a single bond or the like; R is a C 1-20 linear, branched or cyclic hydrocarbon group; and a is 0 or 1).
    提供一种新颖的二胺,以及使用它的聚酰亚胺前体和聚酰亚胺。一种由式(1)表示的二胺:其中X1和X5中的每一个独立的,是单键或类似物;X2和X4中的每一个独立的,是—CH2—或类似物;X3是C1-6烷基或类似物;Y1和Y2中的每一个独立的,是单键或类似物;R是C1-20线性、支链或环烃基;a为0或1。
  • [EN] METHODS AND COMPOUNDS FOR RESTORING MUTANT P53 FUNCTION<br/>[FR] MÉTHODES ET COMPOSÉS POUR LA RESTAURATION D'UNE FONCTION DE MUTANTS DE P53
    申请人:PMV PHARMACEUTICALS INC
    公开号:WO2021262596A1
    公开(公告)日:2021-12-30
    Mutations in oncogenes and tumor suppressors contribute to the development and progression of cancer. The present disclosure describes compounds and methods that restore DNA binding affinity of p53 mutants. The compounds of the present disclosure can bind to mutant p53 and restore the ability of the p53 mutant to bind DNA and activate downstream effectors involved in tumor suppression. The disclosed compounds can be used to reduce the progression of cancers that contain a p53 mutation.
    癌基因和肿瘤抑制基因的突变促进了癌症的发展和进展。本公开描述了一种恢复p53突变体DNA结合亲和力的化合物和方法。本公开的化合物可以结合突变的p53,并恢复p53突变体结合DNA和激活与肿瘤抑制有关的下游效应子的能力。公开的化合物可用于减少含有p53突变的癌症的进展。
  • Diaminobenzobisthiazoles and related compounds
    作者:Justus K. Landquist
    DOI:10.1039/j39670002212
    日期:——
    In the preparation of benzobisthiazoles from m- and p-phenylenediamines by thiocyanation or by ring closure of derived thioureas the linear tricyclic compound is usually the major or the only product. 3,6-Diamino-1,2-phenylene di(hydrogen thiosulphate)(the so-called p-phenylenediamino-2,5-bisthiosulphuric acid) is the 2,3-isomer and correction is required to structures assigned to its derivatives,
    在制备benzobisthiazoles的从米-和p由硫氰化或由派生硫脲环合苯二胺的线性三环类化合物通常是主要的或唯一的产品。3,6-二氨基-1,2-亚苯基二硫代硫酸氢盐(所谓的对-苯二氨基-2,5-双硫代硫酸)是2,3-异构体,需要对其衍生物的结构进行校正,例如,二氨基苯二硫醇,双重氮硫醚和某些苯并二噻唑。在2-萘胺和6-氨基喹啉的衍生物中稠合的噻唑环的形成分别发生在1-和5-位。
  • [EN] PHOSPHINYL AMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS<br/>[FR] COMPOSÉS DE PHOSPHINYLAMIDINE, COMPLEXES DE MÉTAL, SYSTÈMES DE CATALYSEUR, ET LEUR UTILISATION POUR OLIGOMÉRISER OU POLYMÉRISER DES OLÉFINES
    申请人:CHEVRON PHILLIPS CHEMICAL CO
    公开号:WO2011082192A1
    公开(公告)日:2011-07-07
    N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, N2-phosphinyl amidinate metal salt complexes are described. Methods for making N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, and N2-phosphinyl amidinate metal salt complexes are also disclosed. Catalyst systems utilizing the N2-phosphinyl amidine metal salt complexes and N2-phosphinyl amidinate metal salt complexes are also disclosed along with the use of the N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, and N2-phosphinyl amidinate metal salt complexes for the oligomerization and/or polymerization of olefins.
    描述了N2-膦胺化合物、N2-膦胺酸盐、N2-膦胺金属盐络合物、N2-膦胺酸盐金属盐络合物。还公开了制备N2-膦胺化合物、N2-膦胺酸盐、N2-膦胺金属盐络合物和N2-膦胺酸盐金属盐络合物的方法。还公开了利用N2-膦胺金属盐络合物和N2-膦胺酸盐金属盐络合物的催化剂系统,以及利用N2-膦胺化合物、N2-膦胺酸盐、N2-膦胺金属盐络合物和N2-膦胺酸盐金属盐络合物进行烯烃的寡聚和/或聚合的用途。
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