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(1R,3R)-1,3-环己烷二甲酸 | 2305-30-8

中文名称
(1R,3R)-1,3-环己烷二甲酸
中文别名
反式-1,3-环己烷二甲酸
英文名称
trans-1,3-cyclohexanedicarboxylic acid
英文别名
trans-Cyclohexane-1,3-dicarboxylic acid;(1R,3R)-cyclohexane-1,3-dicarboxylic acid
(1R,3R)-1,3-环己烷二甲酸化学式
CAS
2305-30-8
化学式
C8H12O4
mdl
——
分子量
172.181
InChiKey
XBZSBBLNHFMTEB-PHDIDXHHSA-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

  • 熔点:
    147-148 °C
  • 沸点:
    332.4±25.0 °C(Predicted)
  • 密度:
    1.314±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.96
  • 重原子数:
    12.0
  • 可旋转键数:
    2.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    74.6
  • 氢给体数:
    2.0
  • 氢受体数:
    2.0

安全信息

  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H315,H319,H335

SDS

SDS:bc29e7f849551d0b1fbe11e9d64d22cc
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反应信息

  • 作为反应物:
    描述:
    (1R,3R)-1,3-环己烷二甲酸 在 dimethyl sulfide borane 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以83.63%的产率得到(1R,3R)-cyclohexane-1,3-diyldimethanol
    参考文献:
    名称:
    [EN] ANALOGUES OF PENTAMIDINE AND METHODS FOR TREATING INFECTIONS
    [FR] ANALOGUES DE PENTAMIDINE ET MÉTHODES DE TRAITEMENT D'INFECTIONS
    摘要:
    本公开提供了一组胍类类似物及其药学上可接受的盐,用于治疗细菌或真菌感染。感染可能包括由革兰氏阴性细菌、革兰氏阳性细菌或真菌引起的感染。本文还披露了组合物、合成相同的方法以及治疗细菌或真菌感染的方法。
    公开号:
    WO2022087636A1
  • 作为产物:
    参考文献:
    名称:
    MATSUSHITA, HAJIME;NEGISHI, EI-ICHI, J. CHEM. SOC. CHEM. COMMUN., 1982, N 3, 160-161
    摘要:
    DOI:
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文献信息

  • METHOD FOR PRODUCING TRANS-BIS(AMINOMETHYL)CYCLOHEXANE, METHOD FOR PRODUCING BIS(ISOCYANATOMETHYL)CYCLOHEXANE, BIS(ISOCYANATOMETHYL)CYCLOHEXANE, POLYISOCYANATE COMPOSITION, AND POLYURETHANE RESIN
    申请人:MITSUI CHEMICALS, INC.
    公开号:US20160207875A1
    公开(公告)日:2016-07-21
    A method for producing trans-bis(aminomethyl)cyclohexane includes a trans-isomerization step in which cis-dicyanocyclohexane is isomerized into trans-dicyanocyclohexane by heating dicyanocyclohexane containing cis-dicyanocyclohexane in the presence of a tar component produced by distillation of dicyanocyclohexane; and an aminomethylation step in which trans-dicyanocyclohexane produced by the trans-isomerization step is allowed to contact with hydrogen to produce trans-bis(aminomethyl)cyclohexane.
    生产反式-双(甲基)环己烷的方法包括以下步骤:在一个反式异构化步骤中,通过加热含有顺-二环己烷的二环己烷,在二环己烷的蒸馏产生的焦油组分的存在下,将顺-二环己烷异构化为反-二环己烷;以及在一个甲基化步骤中,通过让通过反式异构化步骤产生的反-二环己烷与氢接触来产生反式-双(甲基)环己烷
  • COMPOUNDS AND THEIR METHODS OF USE
    申请人:Lemieux Rene M.
    公开号:US20140142081A1
    公开(公告)日:2014-05-22
    Compounds and compositions comprising compounds that inhibit glutaminase are described herein. Also described herein are methods of using the compounds that inhibit glutaminase in the treatment of cancer.
    本文描述了含有抑制谷酸酶的化合物和组合物。本文还描述了利用这些抑制谷酸酶的化合物治疗癌症的方法。
  • [EN] BIARYLETHER IMIDAZOPYRAZINE BTK INHIBITORS<br/>[FR] COMPOSÉS BIARYLÉTHER IMIDAZOPYRAZINE UTILISÉS COMME INHIBITEURS DE LA BTK
    申请人:MERCK SHARP & DOHME
    公开号:WO2016109219A1
    公开(公告)日:2016-07-07
    The present invention provides Bruton's Tyrosine Kinase (Btk) inhibitor compounds according to Formula (I), or pharmaceutically acceptable salts thereof, or to pharmaceutical compositions comprising these compounds and to their use in therapy. In particular, the present invention relates to the use of Btk inhibitor compounds of Formula (I) in the treatment of Btk mediated disorders.
    本发明提供了根据化学式(I)提供的Bruton酪氨酸激酶(Btk)抑制剂化合物,或其药学上可接受的盐,或包含这些化合物的药物组合物,并且用于治疗的使用。具体而言,本发明涉及在治疗Btk介导的疾病中使用化合物的化学式(I)的Btk抑制剂
  • FUNCTIONALIZED HIGHLY BRANCHED MELAMINE-POLYAMINE POLYMERS
    申请人:Peretolchin Maxim
    公开号:US20120252987A1
    公开(公告)日:2012-10-04
    The present invention relates to a method for producing amphiphilic functionalized highly branched melamine-polyamine polymers by condensing melamine and optionally a melamine derivate having at least one different amine having at least two primary amino groups and optionally also with urea and/or at least one urea derivative and/or with at least one at least difunctional diisocyanate or polyisocyanate and/or at least one carbolic acid having at least two carboxyl groups or at least one derivative thereof, optionally quaternizing a portion of the amino groups of the polymer thereby obtained, reacting the polymer thus obtained with at least one compound capable of undergoing a condensation or addition reaction with amino groups, and optionally quaternizing at least part of the amino groups of the polymer obtained in the first step. The invention further relates to the amphiphilic functionalized highly branched melamine-polyamine polymers that can be obtained by the method according to the invention, and to the use thereof as surface active agents.
    本发明涉及一种通过将三聚氰胺和至少一种具有至少两个主要基的不同基的三聚氰胺生物以及可能还包括尿素和/或至少一种尿素生物和/或至少一种至少双官能团二异氰酸酯或多异氰酸酯和/或至少一种至少具有两个羧基的羧酸或其衍生物缩合,从而制备含有两性功能化的高支化三聚氰胺-多胺聚合物的方法。可选地,对所获得的聚合物的部分基进行季化,然后将所获得的聚合物与至少一种能够与基发生缩合或加成反应的化合物反应,并可选地对第一步中获得的聚合物的部分基进行季化。本发明还涉及通过本发明的方法可以获得的含有两性功能化的高支化三聚氰胺-多胺聚合物,以及将其用作表面活性剂的用途。
  • METHOD FOR PRODUCING BIS(AMINOMETHYL)CYCLOHEXANES
    申请人:Yoshimura Naritoshi
    公开号:US20130197269A1
    公开(公告)日:2013-08-01
    A method for producing bis(aminomethyl)cyclohexanes includes a nuclear hydrogenation step of producing hydrogenated phthalic acids or phthalic acid derivatives by nuclear hydrogenation of phthalic acids or phthalic acid derivatives of at least one selected from the group consisting of phthalic acids, phthalic acid esters, and phthalic acid amides; a cyanation step of treating the hydrogenated phthalic acids or phthalic acid derivatives obtained in the nuclear hydrogenation step with ammonia, thereby producing dicyanocyclohexanes; and an aminomethylation step of treating the dicyanocyclohexanes obtained in the cyanation step with hydrogen, thereby producing bis(aminomethyl)cyclohexanes. In the cyanation step, metal oxide is used as a catalyst, and the obtained dicyanocyclohexanes have a metal content of 3000 ppm or less.
    一种生产双(甲基)环己烷的方法,包括以下步骤:核氢化步骤,通过对邻苯二甲酸邻苯二甲酸生物进行核氢化,得到氢化的邻苯二甲酸邻苯二甲酸生物,所述邻苯二甲酸邻苯二甲酸生物至少选自邻苯二甲酸邻苯二甲酸酯和邻苯二甲酸酰胺组成的群体;青化步骤,将在核氢化步骤中获得的氢化邻苯二甲酸邻苯二甲酸生物处理,从而产生二环己烷甲基化步骤,将在青化步骤中获得的二环己烷与氢处理,从而产生双(甲基)环己烷。在青化步骤中,使用金属氧化物作为催化剂,所获得的二环己烷属含量为3000 ppm或更低。
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