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1,2-dihydroxy-7-methylnaphthalene

中文名称
——
中文别名
——
英文名称
1,2-dihydroxy-7-methylnaphthalene
英文别名
7-Methylnaphthalene-1,2-diol
1,2-dihydroxy-7-methylnaphthalene化学式
CAS
——
化学式
C11H10O2
mdl
——
分子量
174.199
InChiKey
SMDGYHQKMKWCIK-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):
    2.8
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    1,2-dihydro-1,2-dihydroxy-7-methylnaphthalene 在 Escerichia coli recombinant strain JM109(pPS1778) 作用下, 以 为溶剂, 生成 1,2-dihydroxy-7-methylnaphthalene
    参考文献:
    名称:
    Bioconversion of Substituted Naphthalenes to the Corresponding 1,2-Dihydroxy Derivatives by Escherichia coli Recombinant Strains
    摘要:
    1,2-dihydroxynaphthalenes are produced by bioconversion of the corresponding hydrocarbons using Escherichia coli recombinant strains containing the naphthalene dioxygenase and dehydrogenase genes cloned from Pseudomonas fluorescens N3. Conversions are lead by a two step procedure without isolation of the dihydrodiol intermediate. Conversion rates depend on the position and nature of the naphthalene substituent (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4039(97)01404-4
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文献信息

  • SOLUBLE LATE TRANSITION METAL CATALYSTS FOR OLEFIN OLIGOMERIZATIONS III
    申请人:ExxonMobil Chemical Patents Inc.
    公开号:EP1620447A1
    公开(公告)日:2006-02-01
  • SURFACE PRIMER COMPOSITIONS AND METHODS OF USE
    申请人:ACatechol, Inc.
    公开号:US20170217999A1
    公开(公告)日:2017-08-03
    In one embodiment, the present application discloses a surface binding compound of the Formula I or Formula II: wherein the variables EG, EG1, SP1, SP2, SP3, Ar and BG are as defined herein. In another embodiment, the application discloses a method for forming a coating on a surface of a substrate using the surface binding compound of the Formula I or Formula II.
  • [EN] SOLUBLE LATE TRANSITION METAL CATALYSTS FOR OLEFIN OLIGOMERIZATIONS III<br/>[FR] CATALYSEURS A BASE DE METAUX DE TRANSITION TARDIFS SOLUBLES POUR OLIGOMERISATIONS III D'OLEFINES
    申请人:EXXONMOBIL CHEM PATENTS INC
    公开号:WO2003102006A1
    公开(公告)日:2003-12-11
    A series of soluble a-diimine late transition metal catalysts has been invented comprising a substituted or unsubstituted catecholate ligand. The catalysts demon­strate high activity and selectivity for linear a-olefins. As such, these catalysts con­veniently oligomerize ethylene. Typical activators as known to those of ordinary skill in the art are used to activate these transition metal catalysts. These catalysts can be used in a supported or unsupported form.
  • Bioconversion of Substituted Naphthalenes to the Corresponding 1,2-Dihydroxy Derivatives by Escherichia coli Recombinant Strains
    作者:Patrizia Di Gennaro、Giuseppina Bestetti、Enrica Galli、Fulvia Orsini、Francesca Pelizzoni、Guido Sello
    DOI:10.1016/s0040-4039(97)01404-4
    日期:1997.9
    1,2-dihydroxynaphthalenes are produced by bioconversion of the corresponding hydrocarbons using Escherichia coli recombinant strains containing the naphthalene dioxygenase and dehydrogenase genes cloned from Pseudomonas fluorescens N3. Conversions are lead by a two step procedure without isolation of the dihydrodiol intermediate. Conversion rates depend on the position and nature of the naphthalene substituent (C) 1997 Elsevier Science Ltd.
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