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5-(3-t-butyldimethylsiloxyphenyl)-4-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran | 594859-95-7

中文名称
——
中文别名
——
英文名称
5-(3-t-butyldimethylsiloxyphenyl)-4-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran
英文别名
11-[2-[5-[3-[tert-butyl(dimethyl)silyl]oxyphenyl]-3,3-dimethyl-2H-furan-4-yl]-2-methylpropoxy]undecanoic acid
5-(3-t-butyldimethylsiloxyphenyl)-4-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran化学式
CAS
594859-95-7
化学式
C33H56O5Si
mdl
——
分子量
560.89
InChiKey
QFGRHYBSPLJDHR-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):
    9.48
  • 重原子数:
    39
  • 可旋转键数:
    18
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    65
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    咪唑 、 4-(13-carbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-5-(3-hydroxyphenyl)-3,3-dimethyl-2,3-dihydrofuran 以 正己烷乙酸乙酯N,N-二甲基甲酰胺 为溶剂, 以87.4%的产率得到5-(3-t-butyldimethylsiloxyphenyl)-4-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran
    参考文献:
    名称:
    1, 2-Dioxetane derivatives and reagents employing them
    摘要:
    Ar是一个可能带有烷基,芳香基,卤素原子,烷氧基,羧基,甲酰基,烷基酯,芳基酯,烷基酮,芳基酮或异环与之结合的芳基,X是能够标记有机化合物或生物分子的取代基,或酯,Y是氢原子,酰基或式—Si(R4R5R6)的基团(其中R4、R5和R6各自独立,是烷基或芳基),Z是烷基,芳基,氧原子,硫原子,羰基,—(CO)—O—,—O—(CO)—,—NH—,—NH—CO—,—CO—NH—,—OSi(R7R8)—(其中R7和R8各自独立,是烷基或芳基)或式—(R9R10)SiO—(其中R9和R10各自独立,是烷基或芳基),R1和R2各自是烷基或芳基,R3是一个间隔物。
    公开号:
    US20030207329A1
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文献信息

  • 1, 2-Dioxetane derivatives and reagents employing them
    申请人:TOSOH CORPORATION
    公开号:US20030207329A1
    公开(公告)日:2003-11-06
    A 1,2-dioxetane derivative of the formula (I): 1 wherein Ar is an aryl group which may have an alkyl group, an aryl group, a halogen atom, an alkoxyl group, a carboxyl group, a formyl group, an alkyl ester, an aryl ester, an alkylketone, an arylketone or a hetero ring bonded thereto, X is a substituent capable of labeling an organic compound or a biological molecule, or an ester, Y is a hydrogen atom, an acyl group or a group of the formula —Si(R 4 R 5 R 6 ) (wherein each of R 4 , R 5 and R 6 which are independent of one another, is an alkyl group or an aryl group), Z is an alkyl group, an aryl group, an oxygen atom, a sulfur atom, a carbonyl group, —(CO)—O—, —O—(CO)—, —NH—, —NH—CO—, —CO—NH—, —OSi(R 7 R 8 )— (wherein each of R 7 and R 8 which are independent of each other, is an alkyl group or aryl group) or a group of the formula —(R 9 R 10 )SiO— (wherein each of R 9 and R 10 which are independent of each other, is an alkyl group or an aryl group), each of R 1 and R 2 is an alkyl group or an aryl group, and R 3 is a spacer.
    Ar是一个可能带有烷基,芳香基,卤素原子,烷氧基,羧基,甲酰基,烷基酯,芳基酯,烷基酮,芳基酮或异环与之结合的芳基,X是能够标记有机化合物或生物分子的取代基,或酯,Y是氢原子,酰基或式—Si(R4R5R6)的基团(其中R4、R5和R6各自独立,是烷基或芳基),Z是烷基,芳基,氧原子,硫原子,羰基,—(CO)—O—,—O—(CO)—,—NH—,—NH—CO—,—CO—NH—,—OSi(R7R8)—(其中R7和R8各自独立,是烷基或芳基)或式—(R9R10)SiO—(其中R9和R10各自独立,是烷基或芳基),R1和R2各自是烷基或芳基,R3是一个间隔物。
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