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β-(2-furfuril-5-metil)propionato di etile | 1907-79-5

中文名称
——
中文别名
——
英文名称
β-(2-furfuril-5-metil)propionato di etile
英文别名
Ethyl 1-(5-methyl-2-furyl)propionate;3-(5-methyl-furan-2-yl)-propionic acid ethyl ester;3-(5-methyl-[2]furyl)-propionic acid ethyl ester;3-(5-Methyl-[2]furyl)-propionsaeure-aethylester;3-(5-Methyl-<2>furyl)-propionsaeure-ethylester;Ethyl 3-(5-methyl-2-furanyl)propionate;ethyl 3-(5-methylfuran-2-yl)propanoate
β-(2-furfuril-5-metil)propionato di etile化学式
CAS
1907-79-5
化学式
C10H14O3
mdl
——
分子量
182.219
InChiKey
LUTKYWPEMVIBAA-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:
    102.0-102.5 °C(Press: 9.5 Torr)
  • 密度:
    1.0336 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    13
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    39.4
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Therapeutic phenoxyalkylpyridazines and intermediates therefor
    申请人:Sanofi, S.A.
    公开号:US05665763A1
    公开(公告)日:1997-09-09
    Compounds of the formula ##STR1## wherein: R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are as defined in the specification, Y is alkylene of 3 to 9 carbon atoms, R.sub.5 is alkoxycarbonyl, alkyltetrazolyl, phenyl or a heterocycle chosen from benzoxazolyl, benzathiazolyl, thiadiazolyl, imidazolyl, dihydroimidazolyl, oxazolyl, thiazolyl, oxadiazolyl, pyrazolyl, oxazolinyl, isoxazolyl, isothiazolyl, furyl, triazolyl, thiophenyl, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl or any of the above substituted with alkyl, alkoxyalkyl, cycloalkyl, halo alkyl, hydroxyalkyl, alkoxy, hydroxy, halo, furyl, thienyl, fluoroalkyl; or a pharmaceutically acceptable acid addition salts thereof; N-oxides thereof, are useful as antipirconaviral agents.
    式子为##STR1##的化合物,其中:R.sub.1、R.sub.2、R.sub.3和R.sub.4如规范中所定义,Y为3至9个碳原子的烷基,R.sub.5为烷氧羰基,烷基四唑基,苯基或从苯并噁唑基,苯并噻唑基,噻二唑基,咪唑基,二氢咪唑基,噁唑基,噻唑基,噁二唑基,吡唑基,噁唑啉基,异噁唑基,异噻唑基,呋喃基,三唑基,噻吩基,氟烷基取代的上述任何一个杂环;或其药学上可接受的酸盐;其N-氧化物,可用作抗病毒药剂。
  • Therapeutic phenoxyalklpyridazines and intermediates therefor
    申请人:Sterling Winthrop Inc.
    公开号:US05514679A1
    公开(公告)日:1996-05-07
    Compounds of the formula ##STR1## wherein: R.sub.1 and R.sub.2 are independently hydrogen, halo, alkyl, alkenyl, alkoxy, hydroxy, hydroxyalkyl, hydroxyhaloalkyl, alkoxyalkyl, alkylthioalkynyl, hydroxyalkoxy, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, amino, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, alkoxycarbonyl, carboxy or cyanomethyl, nitro, difluoromethyl, trifluoromethyl or cyano; Y is alkylene of 3 to 9 carbon atoms; R.sub.3 and R.sub.4 are independently hydrogen, alkyl, alkoxy, hydroxy, cycloalkyl, hydroxyalkyl, hydroxyhaloalkyl, alkoxyalkyl, hydroxyalkoxy, alkylthioalkyl, alkanoyl, alkanoyloxy, alkylsulfinylalkyl, alkylsulfonylalkyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, alkoxycarbonyl, carboxy, cyanomethyl, fluoroalkyl, cyano, phenyl, alkynyl, alkene, or halo; R.sub.5 is alkoxycarbonyl, alkyltetrazolyl, phenyl or a heterocycle; or a pharmaceutically acceptable acid addition salts thereof; N-oxides thereof, are useful as antipirconaviral agents.
    式为##STR1##的化合物,其中:R.sub.1和R.sub.2是独立的氢,卤素,烷基,烯基,烷氧基,羟基,羟基烷基,羟基卤代烷基,烷氧基烷基,烷硫基炔基,羟基烷氧基,烷硫基烷基,烷基亚磺酰基烷基,烷基磺酰基烷基,氨基,氨基烷基,烷基氨基烷基,二烷基氨基烷基,烷氧羰基,羧基或氰甲基,硝基,二氟甲基,三氟甲基或氰基; Y为3至9个碳原子的烷基;R.sub.3和R.sub.4是独立的氢,烷基,烷氧基,羟基,环烷基,羟基烷基,羟基卤代烷基,烷氧基烷基,羟基烷氧基,烷硫基烷基,脂肪酰基,脂肪酰氧基,烷基亚磺酰基烷基,烷基磺酰基烷基,烷基氨基烷基,二烷基氨基烷基,烷氧羰基,羧基,氰甲基,氟代烷基,氰基,苯基,炔基,烯基或卤素; R.sub.5为烷氧羰基,烷基四唑基,苯基或杂环基;或其药学上可接受的酸加成盐;其N-氧化物,可用作抗皮质醇病毒药物。
  • Heterocycle substituted phenoxyalkylheterocycles and their use as
    申请人:Sterling Winthrop, Inc.
    公开号:US05567717A1
    公开(公告)日:1996-10-22
    A compound of the formula ##STR1## wherein Y, R.sub.1, R.sub.2, R.sub.3, R.sub.4 and R.sub.5 are as defined in the specification.
    该化合物的化学式为##STR1## 其中Y,R.sub.1,R.sub.2,R.sub.3,R.sub.4和R.sub.5的定义见说明书。
  • Reaction of furan compounds with hydrogen sulfide and aspects of its application
    作者:V. G. Kharchenko、T. I. Gubina、S. P. Voronin、I. A. Markushina
    DOI:10.1007/bf00471795
    日期:1986.11
  • Kharchenko, V. G.; Markushina, I. A.; Gubina, T. I., Doklady Chemistry, 1980, vol. 255, p. 601 - 602
    作者:Kharchenko, V. G.、Markushina, I. A.、Gubina, T. I.
    DOI:——
    日期:——
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