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3-亚甲基环丁烷羰酰氯 | 98198-78-8

中文名称
3-亚甲基环丁烷羰酰氯
中文别名
——
英文名称
3-methylenecyclobutanecarboxylic acid chloride
英文别名
3-Methylenecyclobutanecarbonyl chloride;3-methylidenecyclobutane-1-carbonyl chloride
3-亚甲基环丁烷羰酰氯化学式
CAS
98198-78-8
化学式
C6H7ClO
mdl
——
分子量
130.574
InChiKey
DCQFBXFATWSKAA-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:
    36-40 °C(Press: 20 Torr)
  • 密度:
    1.15±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    8
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2916209090

SDS

SDS:1f6a130719f79bea66f620ee0a7d5364
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上下游信息

  • 下游产品
    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:
    3-亚甲基环丁烷羰酰氯4-二甲氨基吡啶 三正丁基氢锡2-mercaptopyridine-1-oxide sodium salt 作用下, 以 various solvent(s) 为溶剂, 反应 2.0h, 生成 亚甲基环丁烷
    参考文献:
    名称:
    Experimental and calculated activation parameters for ring opening of the 1-bicyclo[1.1.1]pentyl radical: the effect of bridgehead substituents
    摘要:
    Ring opening of the 1-bicyclo[1.1.1]pentyl, 3-pentyl-1-bicyclo[1.1.1]pentyl, and 3-carbomethoxy-1-bicyclo[1.1.1]pentyl radicals has been studied by experiment and by molecular orbital theory. Our results indicate that the parent system 1a is extremely reluctant to ring open, with an energy barrier of at least 26 kcal mol-1. The ester- and phenyl-substituted radicals rearrange somewhat more readily, with barriers of about 25 and 21 kcal mol-1, respectively. This trend is also observed in the molecular orbital treatment of these processes. Previous reports that include radical rearrangements of this type must now be reconsidered in light of our new data.
    DOI:
    10.1021/jo00015a018
  • 作为产物:
    描述:
    3-亚甲基环丁基甲腈N,N-二甲基甲酰胺 草酰氯 、 potassium hydroxide 作用下, 以 乙醇二氯甲烷 为溶剂, 反应 4.0h, 生成 3-亚甲基环丁烷羰酰氯
    参考文献:
    名称:
    CYCLOBUTANE AND METHYLCYCLOBUTANE DERIVATIVES AS JANUS KINASE INHIBITORS
    摘要:
    本发明涉及环丁烷和甲基环丁烷衍生物,以及它们的盐、组合物和使用方法,这些是一种Janus激酶(JAK)抑制剂,适用于治疗与JAK相关的疾病,包括炎症性和自身免疫性疾病,以及癌症和骨髓增生性疾病。
    公开号:
    US20110207754A1
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文献信息

  • [EN] CYCLOHEXYL ACID TRIAZOLE AZOLES AS LPA ANTAGONISTS<br/>[FR] AZOLES TRIAZOLES D'ACIDE CYCLOHEXYLE UTILISÉS EN TANT QU'ANTAGONISTES DE LPA
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2019126094A1
    公开(公告)日:2019-06-27
    The present invention provides compounds of Formula (I): Formula (I) or a stereoisomer, tautomer, or pharmaceutically acceptable salt or solvate thereof, wherein all the variables are as defined herein. These compounds are selective LPA receptor inhibitors.
    本发明提供了化合物的结构式(I):结构式(I)或其立体异构体、互变异构体或药学上可接受的盐或溶剂,其中所有变量如本文所定义。这些化合物是选择性LPA受体抑制剂。
  • Benzothiazole cyclobutyl amine derivatives
    申请人:Cowart D. Marlon
    公开号:US20070066588A1
    公开(公告)日:2007-03-22
    Compounds of formula (I) are useful in treating conditions or disorders prevented by or ameliorated by histamine-3 receptor ligands. Also disclosed are pharmaceutical compositions comprising the histamine-3 receptor ligands, methods for using such compounds and compositions, and a process for preparing compounds within the scope of formula (I).
    公式(I)的化合物在治疗由组胺-3受体配体预防或改善的疾病或疾病中是有用的。还公开了包含组胺-3受体配体的药物组合物,使用这类化合物和组合物的方法,以及制备公式(I)范围内化合物的过程。
  • CYCLOBUTANE AND METHYLCYCLOBUTANE DERIVATIVES AS JANUS KINASE INHIBITORS
    申请人:Li Yun-Long
    公开号:US20110207754A1
    公开(公告)日:2011-08-25
    The present invention relates to cyclobutane and methylcyclobutane derivatives, as well as their salts, compositions, and methods of use, which are Janus kinase (JAK) inhibitors useful in the treatment of JAK-associated diseases including, for example, inflammatory and autoimmune disorders, as well as cancer and myeloproliferative disorders.
    本发明涉及环丁烷和甲基环丁烷衍生物,以及它们的盐、组合物和使用方法,这些是一种Janus激酶(JAK)抑制剂,适用于治疗与JAK相关的疾病,包括炎症性和自身免疫性疾病,以及癌症和骨髓增生性疾病。
  • Small-Ring Compounds. XV. Methylenecyclobutene and Related Substances<sup>1</sup>
    作者:Douglas E. Applequist、John D. Roberts
    DOI:10.1021/ja01597a040
    日期:1956.8
    Methylenecyclobutene has been synthesized from diethyl methylenemalonate by way of 3-methylenecyclobutanecarboxylic acid and 3-rnethylenecyclobutylamine. The synthesis featured the use of anthracene as a blocking group for the exocyclic double bond during malonic-ester closure of the cyclobutane ring. 4,4-Dimethyl-3-methylenecyclobutene has been obtained by degradation of α-pinene and 1-phenyl-3-methylenecyclobutene
    亚甲基环丁烯由亚甲基丙二酸二乙酯通过3-亚甲基环丁烷羧酸和3-亚甲基环丁胺合成。该合成的特点是在环丁烷环的丙二酸酯闭合过程中使用蒽作为环外双键的封闭基团。4,4-二甲基-3-亚甲基环丁烯是由α-蒎烯和1-苯基-3-亚甲基环丁烯通过丙二烯与苯乙炔缩合得到的。已发现溴加成和亚甲基环丁烯的三种聚合反应按照基于简单分子轨道理论的预测进行。已经制备了 3-亚甲基三亚甲基氧化物,因为它可能在整个环上具有明显的 π 键合,因此很受关注。
  • BENZOTHIAZOLE CYCLOBUTYL AMINE DERIVATIVES
    申请人:Cowart Marlon D.
    公开号:US20090326222A1
    公开(公告)日:2009-12-31
    Compounds of formula (I) are useful in treating conditions or disorders prevented by or ameliorated by histamine-3 receptor ligands. Also disclosed are pharmaceutical compositions comprising the histamine-3 receptor ligands, methods for using such compounds and compositions, and a process for preparing compounds within the scope of formula (I).
    公式(I)的化合物在治疗由组胺-3受体配体预防或改善的疾病或疾病方面非常有用。还公开了包含组胺-3受体配体的药物组合物,使用此类化合物和组合物的方法以及制备公式(I)范围内化合物的过程。
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