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2-(2-Iodoethyl)-2,5,5-trimethyl-1,3-dioxane | 83862-46-8

中文名称
——
中文别名
——
英文名称
2-(2-Iodoethyl)-2,5,5-trimethyl-1,3-dioxane
英文别名
1,3-Dioxane, 2-(2-iodoethyl)-2,5,5-trimethyl-
2-(2-Iodoethyl)-2,5,5-trimethyl-1,3-dioxane化学式
CAS
83862-46-8
化学式
C9H17IO2
mdl
——
分子量
284.137
InChiKey
BPCYYLCHECYFKB-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:
    265.5±15.0 °C(Predicted)
  • 密度:
    1.408±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • Synthesis of (−)-6,7-Dideoxysqualestatin H5 by Carbonyl Ylide Cycloaddition–Rearrangement and Cross-electrophile Coupling
    作者:Younes Fegheh-Hassanpour、Tanzeel Arif、Herman O. Sintim、Hamad H. Al Mamari、David M. Hodgson
    DOI:10.1021/acs.orglett.7b01513
    日期:2017.7.7
    An asymmetric synthesis of (−)-6,7-dideoxysqualestatin H5 is reported. Key features of the synthesis include the following: (1) highly diastereoselective n-alkylation of a tartrate acetonide enolate and subsequent oxidation–hydrolysis to provide an asymmetric entry to a β-hydroxy-α-ketoester motif; (2) facilitation of Rh(II)-catalyzed cyclic carbonyl ylide formation–cycloaddition by co-generation of
    报道了(-)-6,7-二脱氧角鲨烯抑制素H5的不对称合成。合成的主要特征包括:(1)酒石酸丙酮酸酯烯酸酯的高度非对映选择性正烷基化,以及随后的氧化解作用,以提供不对称进入β-羟基-α-酮酸酯基序的功能;(2)通过不饱和的臭氧分解,通过共生成酮和重氮官能团,促进Rh(II)催化的环状羰基内酯的形成-环加成;(3)三羧酸盐核与不饱和侧链之间的立体保持性Ni催化的Csp 3 -Csp 2交亲电子偶联完成了天然产物
  • FUSED BENZOXAZEPINONES AS ION CHANNEL MODULATORS
    申请人:Gilead Sciences, Inc.
    公开号:EP3085694A1
    公开(公告)日:2016-10-26
    The present disclosure relates to compounds that are sodium channel inhibitors and to their use in the treatment of various disease states, including cardiovascular diseases and diabetes.
    本公开涉及作为通道抑制剂的化合物及其在治疗各种疾病(包括心血管疾病和糖尿病)中的用途。
  • Stereoselective total synthesis of (+)-artemisinin, the antimalarial constituent of Artemisia annua L
    作者:Mitchell A. Avery、Wesley K. M. Chong、Clive Jennings-White
    DOI:10.1021/ja00029a028
    日期:1992.1
    A 10-step stereoselective total synthesis of the antimalarial cadinane sesquiterpene (+)-artemisinin (1) is described. Elaboration of (R)-(+)-pulegone to the known sulfoxide 11 was followed by dianion alkylation and desulfurization to provide the trans-2,3-substituted cyclohexanone 7. Homologation to the cyclohexenecarboxaldehyde 6 was followed by a diastereoselective silyl anion addition to afford the silyl acetate 15. Tandem Claisen ester-enolate rearrangement and dianion alkylation furnished the fully functionalized vinylsilane 18 that underwent abnormal ozonolysis and cyclization to provide the natural product 1.
  • [EN] PERFUME SYSTEMS<br/>[FR] SYSTÈMES DE PARFUM
    申请人:PROCTER & GAMBLE
    公开号:WO2013109798A2
    公开(公告)日:2013-07-25
    The present application relates to perfume delivery systems and consumer products comprising perfume delivery systems and or perfume raw materials, as well as processes for making and using such perfume delivery systems and consumer products.
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