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2-butyl-2-methylsuccinic acid | 90647-77-1

中文名称
——
中文别名
——
英文名称
2-butyl-2-methylsuccinic acid
英文别名
2-butyl-2-methyl-succinic acid;2-Butyl-2-methyl-bernsteinsaeure;2-Butyl-2-methylbutanedioic acid
2-butyl-2-methylsuccinic acid化学式
CAS
90647-77-1
化学式
C9H16O4
mdl
——
分子量
188.224
InChiKey
WMCFQEMLVVLZIJ-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):
    1.6
  • 重原子数:
    13
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Novel succinate compounds, compositions and methods of use and preparation
    申请人:——
    公开号:US20020115863A1
    公开(公告)日:2002-08-22
    Novel hydroxamic acid compounds are disclosed. These hydroxamates inhibit peptidyl deformylase (PDF), an enzyme present in prokaryotes. The hydroxymates are useful as antimicrobials and antibiotics. The compounds of the invention display selective inhibition of peptidyl deformylase versus other metalloproteinases such as matrix metalloproteinases (MMPs). Methods of synthesis and of use of the compounds are also disclosed.
    揭示了一种新型羟羧酸化合物。这些羟羧酸酯抑制肽变形酶(PDF),这是一种存在于原核生物中的酶。这些羟羧酸酯可用作抗微生物和抗生素。该发明的化合物表现出对肽变形酶的选择性抑制,而不影响其他蛋白酶如基质蛋白酶(MMPs)。该文还揭示了这些化合物的合成方法和使用方法。
  • [EN] NOVEL SUCCINATE COMPOUNDS, COMPOSITIONS AND METHODS OF USE AND PREPARATION<br/>[FR] NOUVEAUX COMPOSES A BASE DE SUCCINATE, COMPOSITIONS LES CONTENANT, ET PROCEDES D'UTILISATION ET DE PREPARATION DE CEUX-CI
    申请人:VERSICOR INC
    公开号:WO2001044179A1
    公开(公告)日:2001-06-21
    Novel hydroxamic acid compounds of Formula (I) are disclosed. These hydroxamates inhibit peptide deformylase (PDF), an enzyme present in prokaryotes. The hydroxymates are useful as antimicrobials and antibiotics. The compounds of the invention display selective inhibition of peptidyl deformylase versus other metalloproteinases such as matrix metalloproteinases (MMPs). Methods of synthesis and of use of the compounds are also disclosed.
    本发明揭示了式(I)的新型羟酸化合物。这些羟酸盐抑制肽变形酶(PDF),一种存在于原核生物中的酶。这些羟酸盐可用作抗微生物和抗生素。本发明的化合物显示出对肽酰变形酶的选择性抑制,而不是其他蛋白酶如基质蛋白酶(MMPs)。本发明还揭示了这些化合物的合成和使用方法。
  • Flame retardants with high halogen content and low viscosity
    申请人:Albemarle Corporation
    公开号:EP2107079A2
    公开(公告)日:2009-10-07
    A flame retardant formulation which is the combination of at least (1) at least one bromine-containing polyol flame retardant formed from the reaction of (a) tetrabromophthalic anhydride, (b) an aliphatic polyol, and (c) an epoxide, and (2) at least one aliphatic diester of an alkane dicarboxylic acid, with the proviso that the formulation has a viscosity at 25°C of about 20,000 cps or less, and a bromine content of at least about 40 wt%. A flame retardant compound formed from A) tetrabromophthalic anhydride; B) diethylene glycol; C) at least one alpha-omega alkane diol, or at least one alpha-omega alkane diol and at least one aliphatic monool; and D) at least one alkylene oxide; with the proviso that the compound has a viscosity at 25°C of about 60,000 cps or less, and a bromine content of at least about 43 wt%. Polymer compositions formed from (a) a polyurethane or a polyisocyanurate and (b) a formulation of the invention. One process to make a formulation involves heating a mixture of (a), (b), and at least one liquid aliphatic diester of a alkane dicarboxylic acid to form an intermediate composition; and then the intermediate is contacted one or more times with (c) thereby producing the formulation. Optionally, excess (c) is removed.
    一种阻燃剂配方,它至少是以下物质的组合:(1)至少一种含多元醇阻燃剂,由(a)四邻苯二甲酸酐、(b)脂肪族多元醇和(c)环氧化物反应生成;(2)至少一种烷烃羧酸脂肪族二酯,但该配方在 25°C 时的粘度约为 20°C、(2) 烷烃羧酸的至少一种脂肪族二酯,但该制剂在 25°C 时的粘度不超过约 20,000 cps,含量不低于约 40 wt%。由以下物质形成的阻燃化合物:A) 四邻苯二甲酸酐;B) 二甘醇;C) 至少一种α-ω-烷二醇,或至少一种α-ω-烷二醇和至少一种脂族一元醇;以及 D) 至少一种环氧亚烷烃;但条件是该化合物在 25°C 时的粘度约为 60,000 cps 或更低,含量至少约为 43 wt%。由(a)聚酯或聚异酸酯和(b)本发明配方形成的聚合物组合物。制备配方的一种工艺包括加热(a)、(b)和至少一种烷烃羧酸的液态脂肪族二酯类的混合物,以形成中间体组合物;然后将中间体与(c)接触一次或多次,从而制得配方。可选择去除多余的 (c)。
  • Le Moal,H. et al., Bulletin de la Societe Chimique de France, 1964, p. 579 - 584
    作者:Le Moal,H. et al.
    DOI:——
    日期:——
  • Nielsen et al., Acta Chemica Scandinavica (1947), 1959, vol. 13, p. 1943,1951
    作者:Nielsen et al.
    DOI:——
    日期:——
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