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1-(4-bromophenyl)-1-oxopropan-2-yl formate | 481632-29-5

中文名称
——
中文别名
——
英文名称
1-(4-bromophenyl)-1-oxopropan-2-yl formate
英文别名
2-(4-bromophenyl)-1-methyl-2-oxoethyl formate;[1-(4-bromophenyl)-1-oxopropan-2-yl] formate
1-(4-bromophenyl)-1-oxopropan-2-yl formate化学式
CAS
481632-29-5
化学式
C10H9BrO3
mdl
——
分子量
257.084
InChiKey
XCSLVROXLANIRA-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:
    346.8±27.0 °C(Predicted)
  • 密度:
    1.475±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    43.4
  • 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

  • Linking Bisphosphonates to the Free Amino Groups in Fluoroquinolones: Preparation of Osteotropic Prodrugs for the Prevention of Osteomyelitis
    作者:Tom J. Houghton、Kelly S. E. Tanaka、Ting Kang、Evelyne Dietrich、Yanick Lafontaine、Daniel Delorme、Sandra S. Ferreira、Frederic Viens、Francis F. Arhin、Ingrid Sarmiento、Dario Lehoux、Ibtihal Fadhil、Karine Laquerre、Jing Liu、Valérie Ostiguy、Hugo Poirier、Gregory Moeck、Thomas R. Parr、Adel Rafai Far
    DOI:10.1021/jm801007z
    日期:2008.11.13
    Osteomyelitis is an infection located in bone and a notoriously difficult disease to manage, requiring frequent and heavy doses of systemically administered antibiotics. Targeting antibiotics to the bone after systemic administration may provide both greater efficacy of treatment and less frequent administration. By taking advantage, of the affinity of the bisphosphonate group for bone mineral, we have prepared a set of 13 bisphosphonated antibacterial prodrugs based on eight different linkers tethered to the free amino functionality on fluoroquinolone antibiotics. While all but one of the prodrugs were shown in vitro to be effective and rapid bone binders (over 90% in 1 h), only eight of them demonstrated the capacity to significantly regenerate the parent drug. In a rat model of the disease, a selected group of agents demonstrated their ability to prevent osteomyelitis when used in circumstances under which the parent drug had already been cleared and is thus inactive.
  • 2-(2,6-DISUBSTITUTED PHENYL)-4-ARYL-5-ALKYL-1,3-OXAZOLINE COMPOUNDS USEFUL AS INSECTICIDES AND ACARICIDES
    申请人:Dow Agrosciences LLC
    公开号:EP1397353A1
    公开(公告)日:2004-03-17
  • PHOSPHONATED FLUOROQUINOLONES, ANTIBACTERIAL ANALOGS THEREOF, AND METHODS FOR THE PREVENTION AND TREATMENT OF BONE AND JOINT INFECTIONS
    申请人:Targanta Therapeutics Inc.
    公开号:EP1881974A2
    公开(公告)日:2008-01-30
  • US6573286B1
    申请人:——
    公开号:US6573286B1
    公开(公告)日:2003-06-03
  • [EN] 2-(2,6-DISUBSTITUTED PHENYL)-4-ARYL-5-ALKYL-1,3-OXAZOLINE COMPOUNDS USEFUL AS INSECTICIDES AND ACARICIDES<br/>[FR] COMPOSES DE 2-(2,6-PHENYLE DISUBSTITUE)-4-ARYLE-5-ALKYLE-1,3-OYAZOLINE UTILES EN TANT QU'INSECTICIDES ET ACARICIDES
    申请人:DOW AGROSCIENCES LLC
    公开号:WO2003000669A1
    公开(公告)日:2003-01-03
    Oxazoline compounds having a 2,6-disubstituted-phenyl group in the 2-position, an aryl or heteroaryl group in the 4-position and an alkyl group in the 5 position are effective in controlling aphids, insects and mites.
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