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5-Hydroxymethyl-selenophen-2-carbonsaeure | 25744-94-9

中文名称
——
中文别名
——
英文名称
5-Hydroxymethyl-selenophen-2-carbonsaeure
英文别名
5-(Hydroxymethyl)selenophene-2-carboxylic acid;5-(hydroxymethyl)selenophene-2-carboxylic acid
5-Hydroxymethyl-selenophen-2-carbonsaeure化学式
CAS
25744-94-9
化学式
C6H6O3Se
mdl
——
分子量
205.072
InChiKey
NSCGNOAETGOKPK-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):
    -0.07
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    57.5
  • 氢给体数:
    2
  • 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

反应信息

  • 作为反应物:
    描述:
    5-Hydroxymethyl-selenophen-2-carbonsaeure氯化亚砜 作用下, 以 为溶剂, 生成
    参考文献:
    名称:
    Selenosartans: Novel selenophene analogues of milfasartan and eprosartan
    摘要:
    A series of selenophene analogues of the thiophene-containing anti hypertensives milfasartan and eprosartan were prepared and tested for AT(1) receptor antagonist properties. All four selenophene compounds proved to be potent AT(1) receptor antagonists, with pK(B) estimates indicating that these selenides are at least as effective as the thiophene parent compounds at blocking AT(1) receptor mediated responses. These results reveal that replacement of sulfur with selenium in thiophene-containing sartans does not interfere with sartan activity. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.11.136
  • 作为产物:
    描述:
    5-(hydroxymethyl)selenophene-2-carbaldehydesodium hydroxidesilver nitrate 作用下, 以80%的产率得到5-Hydroxymethyl-selenophen-2-carbonsaeure
    参考文献:
    名称:
    Selenosartans: Novel selenophene analogues of milfasartan and eprosartan
    摘要:
    A series of selenophene analogues of the thiophene-containing anti hypertensives milfasartan and eprosartan were prepared and tested for AT(1) receptor antagonist properties. All four selenophene compounds proved to be potent AT(1) receptor antagonists, with pK(B) estimates indicating that these selenides are at least as effective as the thiophene parent compounds at blocking AT(1) receptor mediated responses. These results reveal that replacement of sulfur with selenium in thiophene-containing sartans does not interfere with sartan activity. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.11.136
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文献信息

  • Selenosartans: Novel selenophene analogues of milfasartan and eprosartan
    作者:Rebecca L. Grange、James Ziogas、Andrea J. North、James A. Angus、Carl H. Schiesser
    DOI:10.1016/j.bmcl.2007.11.136
    日期:2008.2
    A series of selenophene analogues of the thiophene-containing anti hypertensives milfasartan and eprosartan were prepared and tested for AT(1) receptor antagonist properties. All four selenophene compounds proved to be potent AT(1) receptor antagonists, with pK(B) estimates indicating that these selenides are at least as effective as the thiophene parent compounds at blocking AT(1) receptor mediated responses. These results reveal that replacement of sulfur with selenium in thiophene-containing sartans does not interfere with sartan activity. (C) 2007 Elsevier Ltd. All rights reserved.
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同类化合物

硒酚 硒吩并[3,2-B]噻吩 硒吩-3-羧酸 硒吩-2-羧酸 硒吩-2-硼酸 5-甲基-2-硒吩羰基氯化物 5-甲基-2-硒吩亚磺酸 3-硒吩羰基氯化物 3-甲基硒吩 3,4-双(氯甲基)-2,5-二甲基硒吩 2-甲基-硒吩 2-乙烯基硒吩 2,5-二-(2'-噻吩基)硒吩 2,2'-双硒 2,6-di(selenophen-2-yl)tetrahydro-4H-selenopyran-4-one 2-(2-(selenophen-2-yl)ethynyl)selenophene (2-selenophene-2-yl)lithium 2-(dec-1-ynyl)selenophene (3-selenienyl)di(1-adamantyl)methanol 5-Methyl-2-mercapto-selenophen seleno[3,4-b]thiophene 3-Selenophenethiol, 2,5-dimethyl- 2-dicyanomethylselenophene bis(3-selenienyl)methanol 2-Propyl-selenophen 2-(5'-hydroxymethyl-2'-selenyl)-thiophene 4,4,6,6-tetramethyl-2-{[(methylsulfonyl)thio]methyl}-4,6-dihydro-5H-selenolo[2,3-c]pyrrol-5-yloxyl radical selenosulflower 5-Carboxyseleno<2,3-b>thiophen methyl 4-[(dimethylamino)diazenyl]-5-methylselenophene-2-carboxylate ethyl selenopheno[3,2-b]thiophene-5-carboxylate 3-Cyanoselenophen 2,4-Ditert-butylselenophene 5-Hydroxymethyl-selenophen-2-carbonsaeure 1,3-Dithiolo<4,5-c>selenophene-2-thione methyl 3-amino-5-(methoxycarbonyl)selenophene-2-carboxylate tetramethyl 2,3,4,5-selenophenetetracarboxylate 2,2'-{5,5'-[5,5'-(selenophene-2,5-diyl)bis(3,4-dibutylthien-5,2-diyl)]bis-(selenophene-5,2-diyl)}bis(methan-1-yl-1-ylidene)dimalononitrile 2-(2-bromoethylsulfonyl)selenophene 2-(4,4-bis(methoxymethyl)-7-(selenophen-2-yl)hepta-1,6-diynyl)selenophene cyclopenta[c]selenophene-(CH2OMe)2 2-[5,5-Bis(methoxymethyl)-3-thiophen-2-yl-4,6-dihydrocyclopenta[c]selenophen-1-yl]thiophene 3,6-dimethylselenolo<3,2-b>selenophene 2,5-Bis(2-selenienyl)furan tetramethyl-selenophene 2,3,4-trimethyl-selenophene 2,3,5-trimethyl-selenophene selenophen-2-yl-methanol 1-selenophen-2-yl-ethanol 2-carbomethoxyselenophene