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2,5-dibromo-3-methyl-hexane | 855907-53-8

中文名称
——
中文别名
——
英文名称
2,5-dibromo-3-methyl-hexane
英文别名
2,5-Dibrom-3-methyl-hexan;2,5-Dibromo-3-methylhexane
2,5-dibromo-3-methyl-hexane化学式
CAS
855907-53-8
化学式
C7H14Br2
mdl
——
分子量
257.996
InChiKey
UBXZJMOQXKOJLT-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):
    3.8
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    2,5-dibromo-3-methyl-hexane硫酸sodium ethanolate 作用下, 生成 1-carbamoyl-2,3,5-trimethyl-cyclopentanecarboxylic acid ethyl ester
    参考文献:
    名称:
    Übercyclische衍生品丙二酰胺。II
    摘要:
    Abstract Es wird die Kondensation von 1,4‐Dihalogenalkanen und Cyanessigester zu alkylsubstituierten 1‐Cyano‐cyclopentancarbonsäureestern und die Verseifung der letzteren zu alkylierten 1‐Carbamylcyclopentancarbonsäureestern beschrieben. Pharmakologisch zeigen der racemische und der meso‐1‐Carbamyl‐2,5‐dimethyl‐cyclopentancarbonsäure‐äthylester in bezug auf ihre narkotischen Eigenschaften und Ihre Toxizität einen deutlichen Unterschied.
    DOI:
    10.1002/hlca.19520350742
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 氢溴酸 作用下, 生成 2,5-dibromo-3-methyl-hexane
    参考文献:
    名称:
    US2561688
    摘要:
    公开号:
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文献信息

  • ORGANO-1-OXA-4-AZONIUM CYCLOHEXANE COMPOUNDS
    申请人:UOP LLC
    公开号:US20160159760A1
    公开(公告)日:2016-06-09
    Novel 1-oxa-4-azonium cyclohexane salts are described. These compounds can be used as structure directing agents, and they overcome many of the typical problems associated with OSDA synthesis and subsequent zeolite synthesis. Methods for synthesis of the 1-oxa-4-azonium cyclohexane salts from a variety of starting materials are also described. A substituted hydrocarbon is added to water to form a mixture, and a 1-oxa-4-azacyclohexane derivative is then added. The reaction mixture stirred until a solution containing the 1-oxa-4-azonium cyclohexane salt is obtained.
    描述了新型的1-oxa-4-azonium环己烷盐。这些化合物可用作结构导向剂,并且克服了与OSDA合成和随后的沸石合成相关许多典型问题。还描述了从各种起始材料合成1-oxa-4-azonium环己烷盐的方法。 将取代的烃加入中形成混合物,然后加入1-oxa-4-azacyclohexane衍生物。搅拌反应混合物,直到获得含有1-oxa-4-azonium环己烷盐的溶液。
  • Organo-1-oxa-4-azonium cyclohexane compounds
    申请人:UOP LLC
    公开号:US10633355B2
    公开(公告)日:2020-04-28
    Novel 1-oxa-4-azonium cyclohexane salts are described. These compounds can be used as structure directing agents, and they overcome many of the typical problems associated with OSDA synthesis and subsequent zeolite synthesis. Methods for synthesis of the 1-oxa-4-azonium cyclohexane salts from a variety of starting materials are also described. A substituted hydrocarbon is added to water to form a mixture, and a 1-oxa-4-azacyclohexane derivative is then added. The reaction mixture stirred until a solution containing the 1-oxa-4-azonium cyclohexane salt is obtained.
    本文介绍了新型 1-oxa-4-azonium 环己烷盐。这些化合物可用作结构引导剂,克服了与 OSDA 合成和后续沸石合成相关的许多典型问题。此外,还介绍了从各种起始材料合成 1-oxa-4-azonium 环己烷盐的方法。将取代的碳氢化合物加入中形成混合物,然后加入 1-oxa-4-azacyclohexane 衍生物。搅拌反应混合物,直到得到含有 1-oxa-4-azium 环己烷盐的溶液。
  • US2561689
    申请人:——
    公开号:——
    公开(公告)日:——
  • ZEOLITES USING AN ORGANO-1-OXA-4-AZONIUMCYCLOHEXANE COMPOUND
    申请人:UOP LLC
    公开号:EP3227233A1
    公开(公告)日:2017-10-11
  • SYNTHESIS OF ZEOLITES USING AN ORGANOAMMONIUM COMPOUND
    申请人:UOP LLC
    公开号:US20150158020A1
    公开(公告)日:2015-06-11
    A method for synthesizing a zeolite includes the steps of: (a) preparing an aqueous mixture comprising water, a substituted hydrocarbon and an amine; (b) reacting the aqueous mixture; (c) obtaining a solution comprising an organoammonium product; (d) forming a reaction mixture including reactive sources of M, Al, Si, optionally seeds of a layered material L, and the solution, wherein M is a metal; and (e) heating the reaction mixture to form the zeolite. The substituted hydrocarbon can be an α,ω-dihalogen substituted alkane, and the amine is preferably essentially incapable of undergoing pyramidal inversion.
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