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4-Isopropoxymethyl-[1,3]dioxolane | 17226-23-2

中文名称
——
中文别名
——
英文名称
4-Isopropoxymethyl-[1,3]dioxolane
英文别名
4-{[(Propan-2-yl)oxy]methyl}-1,3-dioxolane;4-(propan-2-yloxymethyl)-1,3-dioxolane
4-Isopropoxymethyl-[1,3]dioxolane化学式
CAS
17226-23-2
化学式
C7H14O3
mdl
——
分子量
146.186
InChiKey
XQXZTEGVRIBJNR-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):
    0.5
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    27.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    4-Isopropoxymethyl-[1,3]dioxolane三乙基硅烷 生成 Triethyl-(3-isopropoxy-2-methoxy-propoxy)-silane
    参考文献:
    名称:
    MIRONOV, I. V.;MELNITSKIJ, I. A.;SIRAEVA, I. N.;KILADZE, T. K.;KANTOR, E.+, ZH. OBSHCH. XIMII, 1982, 52, N 10, 2284-2288
    摘要:
    DOI:
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文献信息

  • PYRROLIDINYL UREA, PYRROLIDINYL THIOUREA AND PYRROLIDINYL GUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS
    申请人:Allen Shelley
    公开号:US20150166564A1
    公开(公告)日:2015-06-18
    Compounds of Formula I: or stereoisomers, tautomers, or pharmaceutically acceptable salts, or solvates or prodrugs thereof, where R 1 , R 2 , R a , R b , R c , R d , X, Y, B, and Ring C are as defined herein, and wherein the Y—B moiety and the NH—C(═X)—NH moiety are in the trans configuration, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation, neurodegenerative diseases and certain infectious diseases.
    化合物I的公式:或其立体异构体、互变异构体、药学上可接受的盐、溶剂或前药,其中R1、R2、Ra、Rb、Rc、Rd、X、Y、B和环C的定义如本文所述,其中Y-B基团和NH-C(═X)-NH基团处于反式构象,是TrkA激酶的抑制剂,可用于治疗可以通过TrkA激酶抑制剂治疗的疾病,例如疼痛、癌症、炎症、神经退行性疾病和某些传染病。
  • POLYHYDROXYURETHANE MICROPARTICLES, AND PROCESS FOR PRODUCING SAME
    申请人:Dainichiseika Color & Chemicals Mfg. Co., Ltd.
    公开号:EP2706078A1
    公开(公告)日:2014-03-12
    A problem is to provide polyhydroxyurethane microparticles, which have a narrow particle size distribution and are applicable to a wide range of use. Provided are polyhydroxyurethane microparticles which are spherical polymer microparticles having particle sizes of 0.1 µm to 300 µm. A polymer that makes up the polymer microparticles has in a structure thereof chemical structure units represented by the following formula (1) and/or chemical structure units represented by the following formula (2). In the chemical structure units (1) and (2), -O-CO- bonds have been derived from carbon dioxide.
    目前的问题是提供粒径分布窄且适用范围广的聚羟基聚氨酯微粒。本发明提供的聚羟基聚氨酯微粒是球形聚合物微粒,其粒径为 0.1 微米至 300 微米。构成聚合物微粒的聚合物在其结构中具有下式(1)表示的化学结构单元和/或下式(2)表示的化学结构单元。在化学结构单元(1)和(2)中,-O-CO-键来自二氧化碳。
  • Mironov, I. V.; Mel'nitskii, I. A.; Siraeva, I. N., Journal of general chemistry of the USSR, 1982, vol. 52, # 10, p. 2034 - 2037
    作者:Mironov, I. V.、Mel'nitskii, I. A.、Siraeva, I. N.、Kiladze, T. K.、Kantor, E. A.、Rakhmankulov, D. L.
    DOI:——
    日期:——
  • PYRROLIDINYL UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS
    申请人:ARRAY BIOPHARMA INC.
    公开号:US20160297796A1
    公开(公告)日:2016-10-13
    Compounds of Formula (I): or stereoisomers, tautomers, or pharmaceutically acceptable salts, or solvates or prodrugs thereof, where R 1 , R 2 , R a , R b , R c , R d , X, Ring B, and Ring C are as defined herein, and wherein Ring B moiety and the NH—C(═X)—NH moiety are in the trans configuration, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis and pelvic pain syndrome.
  • N-BICYCLIC ARYL,N'-PYRAZOLYL UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS
    申请人:ARRAY BIOPHARMA INC.
    公开号:US20160280681A1
    公开(公告)日:2016-09-29
    Compounds of Formula (I): or stereoisomers, tautomers, or pharmaceutically acceptable salts, solvates or prodrugs thereof, wherein Ring A, Ring C and X are as defined herein, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome.
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