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2-s-Butyl-2-hydroxymethyl-1,3-propanediol | 82515-52-4

中文名称
——
中文别名
——
英文名称
2-s-Butyl-2-hydroxymethyl-1,3-propanediol
英文别名
2-Butan-2-yl-2-(hydroxymethyl)propane-1,3-diol
2-s-Butyl-2-hydroxymethyl-1,3-propanediol化学式
CAS
82515-52-4
化学式
C8H18O3
mdl
——
分子量
162.229
InChiKey
GOMHEPGTRNLWPW-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):
    0.2
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    60.7
  • 氢给体数:
    3
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Bicyclophosphorothionate antagonists exhibiting selectivity for housefly GABA receptors
    摘要:
    2,6,7-Trioxa-1-phosphabicyclo[2.2.2]octane 1-sulfides (bicyclophosphorothionates) with various C1-4 alkyl groups at the 3- and 4-positions were synthesized and tested for their ability to compete with [H-3]4'-ethynyl-4-n-propylbicycloorthobenzoate (EBOB), a non-competitive antagonist of gamma-aminobutyric acid (GABA) receptors, for specific binding to rat-brain and housefly-head membranes, and for their insecticidal activity against houseflies. Among the 3,4-substituted analogues, 20 compounds were selectively active for housefly GABA receptors versus rat GABA receptors. The 3-alkyl groups of C-3 length and the 4-alkyl groups of C-4 length were tolerated in housefly receptors, whereas such bulky substituents were deleterious in rat receptors. The 4-isobutyl-3-isopropyl analogue was the most potent in housefly receptors (IC50 = 45.2 nM), and tert-butylbicyclophosphorothionate (TBPS), with the 4-tert-butyl group and no 3-substituent, was the most potent in rat receptors (IC50 = 62.2 nM). Their receptor selectivities (rat IC50/housefly IC50) were 52 and 0.038, respectively. The insecticidal activity (LD50) of 20 active analogues was well correlated with their potency (IC50) in inhibiting [H-3]EBOB binding to housefly-head membranes (r = 0.93). The results obtained in the present study indicate that the introduction of appropriate alkyl groups into the 3- and ii-positions of bicyclophosphorothionate leads to non-competitive antagonists with increased affinity and selectivity for housefly ionotropic GABA receptors versus rat GABAA receptors. (C) 1999 Society of Chemical Industry.
    DOI:
    10.1002/(sici)1096-9063(199910)55:10<971::aid-ps49>3.0.co;2-j
  • 作为产物:
    描述:
    Diethyl s-butylhydroxymethylmalonate 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 以40%的产率得到2-s-Butyl-2-hydroxymethyl-1,3-propanediol
    参考文献:
    名称:
    Synthesis and some spectral characteristics of bicyclic phosphate, GABA antagonists.
    摘要:
    双环磷酸酯(BPs),即GABA拮抗剂,是通过相应的三醇与磷酰氯反应制备的。这些三醇是通过以下方法之一获得的:(a)具有α氢原子的醛与甲醛的Tollens缩合;(b)以多聚甲醛为反应物的烷基丙二酸酯或α-烷基乙酰乙酸酯的碱催化羟甲基化反应,随后进行还原;(c)二乙基特戊酰基丙二酸酯的还原;或(d)季戊四醇的卤化。一些BPs还可通过BP同系物的官能团修饰得到。4-取代的BPs的1H-NMR谱显示出由于内环亚甲基质子引起的特征双重峰,其位移位置受桥头取代基的电子性质影响。BPs的质谱特征在于环失CH2O的峰。
    DOI:
    10.1271/bbb1961.46.411
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文献信息

  • Curing composition
    申请人:IMPERIAL CHEMICAL INDUSTRIES PLC
    公开号:EP0267698A2
    公开(公告)日:1988-05-18
    A curing composition comprising a silane func­tional acrylic polymer component and a silane functional oligomer component. The polymer component is a co-polymer of functional silyl group-containing units derived from monomers of Formula:-     CH₂=CR¹CO₂(CH₂)aL The oligomer component is of formula     E(GKL)₆ in which E is derived from a multifunctional isocyanate oligomer, G is of general formula:-     -[0(CH₂)₅CO]c[O(CH₂)dOCO(CH₂)₂]- and K is of general formula:-     -[NR⁵(CH₂)m]- and where L is a group of Formula
    一种固化组合物,包括硅烷官能团丙烯酸聚合物组分和硅烷官能团低聚物组分。 聚合物组分是含官能团基单元的共聚物,这些单元来源于式:- CH₂=CR¹CO₂(CH₂)aL 低聚物组分为式 E(GKL)₆,其中 E 来源于多功能异氰酸酯低聚物,G 为通式:-[0(CH₂)₅CO]c[O(CH₂)dOCO(CH₂)₂]-,K 为通式:-[NR⁵(CH₂)m]-,其中 L 为式的基团。
  • OZOE, YOSHIHISA;ETO, MORIFUSA, AGR. AND BIOL. CHEM., 1982, 46, N 2, 411-418
    作者:OZOE, YOSHIHISA、ETO, MORIFUSA
    DOI:——
    日期:——
  • Use Of Aqueous Dispersions For Tertiary Mineral Oil Production
    申请人:Huff Jürgen
    公开号:US20080194434A1
    公开(公告)日:2008-08-14
    Use of water-soluble polymers for tertiary mineral oil production by introducing the polymer into a mineral oil deposit, in which the water-soluble polymers are used in the form of a dispersion of the water-soluble polymer and at least one water-soluble, polymeric stabilizer.
  • US4785035A
    申请人:——
    公开号:US4785035A
    公开(公告)日:1988-11-15
  • US7622428B2
    申请人:——
    公开号:US7622428B2
    公开(公告)日:2009-11-24
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