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2,4-Dimethoxy-6-methyl-benzoic acid (7R,8S,8aS)-8-hydroxy-7-methyl-6-oxo-3-((E)-propenyl)-6,7,8,8a-tetrahydro-1H-isochromen-7-yl ester | 185907-63-5

中文名称
——
中文别名
——
英文名称
2,4-Dimethoxy-6-methyl-benzoic acid (7R,8S,8aS)-8-hydroxy-7-methyl-6-oxo-3-((E)-propenyl)-6,7,8,8a-tetrahydro-1H-isochromen-7-yl ester
英文别名
Falconensin F;[(7R,8S,8aS)-8-hydroxy-7-methyl-6-oxo-3-[(E)-prop-1-enyl]-8,8a-dihydro-1H-isochromen-7-yl] 2,4-dimethoxy-6-methylbenzoate
2,4-Dimethoxy-6-methyl-benzoic acid (7R,8S,8aS)-8-hydroxy-7-methyl-6-oxo-3-((E)-propenyl)-6,7,8,8a-tetrahydro-1H-isochromen-7-yl ester化学式
CAS
185907-63-5
化学式
C23H26O7
mdl
——
分子量
414.455
InChiKey
HEERUVMQLIHKQR-SWEFAHEHSA-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):
    2.7
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    91.3
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Isolation and Structures of New Azaphilone Derivatives, Falconensins E-G, from Emericella falconensis and Absolute Configurations of Falconensins A-G.
    摘要:
    从Emericella falconensis菌丝体中分离出三种新的azaphilone衍生物,分别是falconensins E5 (5)、F (6)和G (7),以及falconensins A (1)、B (2)、C (3)、D (4)和H (8),以及三种hopane型三萜类化合物,分别是zeorin (9)、hepane-7β, 22-diol (10)和hopane-6α, 7β, 22-triol (11)。通过光谱分析和化学相关性,证实了5-7的结构。此外,还确定了falconensins A (1)至G(7)的绝对立体化学结构。
    DOI:
    10.1248/cpb.44.2213
  • 作为产物:
    描述:
    重氮甲烷 、 4-Hydroxy-2-methoxy-6-methyl-benzoic acid (7R,8S,8aS)-8-hydroxy-7-methyl-6-oxo-3-((E)-propenyl)-6,7,8,8a-tetrahydro-1H-isochromen-7-yl ester 以 乙醚 为溶剂, 以2 mg的产率得到2,4-Dimethoxy-6-methyl-benzoic acid (7R,8S,8aS)-8-hydroxy-7-methyl-6-oxo-3-((E)-propenyl)-6,7,8,8a-tetrahydro-1H-isochromen-7-yl ester
    参考文献:
    名称:
    Hydrogenated azaphilones from Emericella falconensis and E. fruticulosa
    摘要:
    DOI:
    10.1016/s0031-9422(98)80085-x
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文献信息

  • Isolation and Structures of New Azaphilone Derivatives, Falconensins E-G, from Emericella falconensis and Absolute Configurations of Falconensins A-G.
    作者:Takeshi ITABASHI、Nobuko OGASAWARA、Koohei NOZAWA、Ken-ichi KAWAI
    DOI:10.1248/cpb.44.2213
    日期:——
    Three new azaphilone derivatives designated falconensins E5 (5), F (6), and G (7) were isolated from the mycelium o Emericella falconensis, along with falconensins A (1), B (2), C (3), D (4), and H (8), and three hopane-type triterpenes, zeorin (9), hepane-7β, 22-diol (10), and hopane-6α, 7β, 22-triol (11). The structures of 5-7 were confirmed by spectroscopic investigation and chemical correlations. The absolute stereochemistry of falconensins A (1) to G(7) was also established.
    从Emericella falconensis菌丝体中分离出三种新的azaphilone衍生物,分别是falconensins E5 (5)、F (6)和G (7),以及falconensins A (1)、B (2)、C (3)、D (4)和H (8),以及三种hopane型三萜类化合物,分别是zeorin (9)、hepane-7β, 22-diol (10)和hopane-6α, 7β, 22-triol (11)。通过光谱分析和化学相关性,证实了5-7的结构。此外,还确定了falconensins A (1)至G(7)的绝对立体化学结构。
  • Hydrogenated azaphilones from Emericella falconensis and E. fruticulosa
    作者:Nobuko Ogasawara、Ken-Ichi Kawai
    DOI:10.1016/s0031-9422(98)80085-x
    日期:1998.3
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同类化合物

萘啶霉素 苯酚,4-(4-吗啉基磺酰)- 焦曲二醇 核丛青霉素 异色酮VI [(7R)-7-甲基-6,8-二氧代-3-[(E)-丙-1-烯基]异苯并吡喃-7-基]2,4-二羟基-6-甲基苯甲酸酯 (E,E,E)-(-)-7-(乙酰氧基)-3-(1,3,5-庚三烯基)-7-甲基-6H-2-苯并吡喃-6,8(7H)-二酮 (7S,8S)-5-氯-3-[(1E,3E)-3,5-二甲基庚-1,3-二烯基]-7,8-二羟基-7-甲基-8H-异苯并吡喃-6-酮 (7R,8R)-5-氯-3-[(1E,3E,5S)-3,5-二甲基庚-1,3-二烯-1-基]-7,8-二羟基-7-甲基-7,8-二氢-6H-异色烯-6-酮 Komaroviquinone entonaemin A 7-heptanoyloxy-3,7-dimethyl-7,8-dihydro-6H-isochromene-6,8-dione sclerketide B (+)-sclerotiorin 2-formyl-1,2-dihydro-6,7,8-trimethoxyisoquinoline Mitorubrinic acid, (S)- (E)-7-hydroxy-7-methyl-3-(prop-1-en-1-yl)-6H-isochromene-6,8(7H)-dione lunatoic acid A (3-Butyl-7-methyl-6,8-dioxoisochromen-7-yl) 6-chloropyridine-3-carboxylate (3-Cyclopropyl-7-methyl-6,8-dioxoisochromen-7-yl) 6-chloropyridine-3-carboxylate [3-(4-Cyanophenyl)-7-methyl-6,8-dioxoisochromen-7-yl] 6-chloropyridine-3-carboxylate (5-Acetyloxy-3-butyl-7-methyl-6,8-dioxoisochromen-7-yl) 6-chloropyridine-3-carboxylate 6-Chloronicotinic acid [6,8-diketo-7-methyl-3-(3-thienyl)isochromen-7-yl] ester Methyl 4-(7-methyl-6,8-dioxo-7-propanoyloxyisochromen-3-yl)butanoate [3-(4-Methoxy-4-oxidanylidene-butyl)-7-methyl-6,8-bis(oxidanylidene)isochromen-7-yl] 6-chloranylpyridine-3-carboxylate [3-(4-Methoxy-4-oxobutyl)-7-methyl-6,8-dioxoisochromen-7-yl] furan-2-carboxylate 4-(7-Hydrocinnamoyloxy-6,8-diketo-7-methyl-isochromen-3-yl)butyric acid methyl ester 4-O-[3-(4-cyanophenyl)-7-methyl-6,8-dioxoisochromen-7-yl] 1-O-methyl butanedioate 1-O-methyl 4-O-(7-methyl-6,8-dioxo-3-thiophen-3-ylisochromen-7-yl) butanedioate 4-O-(5-acetyloxy-3-butyl-7-methyl-6,8-dioxoisochromen-7-yl) 1-O-methyl butanedioate O4-[3-butyl-7-methyl-6,8-bis(oxidanylidene)isochromen-7-yl] O1-methyl butanedioate tert-butyl N-[4-(7-hydroxy-7-methyl-6,8-dioxoisochromen-3-yl)butyl]carbamate 3-(2-(4-fluorophenyl)-6,8-dimethoxy-1-phenyl-1,2-dihydroisoquinolin-3-yl)oxazolidin-2-one 3-(2-(4-chlorophenyl)-6,8-dimethoxy-1-phenyl-1,2-dihydroisoquinolin-3-yl)oxazolidin-2-one 4-Benzyloxy-2-methoxy-6-methyl-benzoic acid (R)-3-((E)-3-hydroxy-propenyl)-7-methyl-6,8-dioxo-7,8-dihydro-6H-isochromen-7-yl ester (-)-mitorubrinic acid 4-Benzyloxy-2-methoxy-6-methyl-benzoic acid (R)-3-((E)-2-tert-butoxycarbonyl-vinyl)-7-methyl-6,8-dioxo-7,8-dihydro-6H-isochromen-7-yl ester 4-Benzyloxy-2-methoxy-6-methyl-benzoic acid (R)-7-methyl-6,8-dioxo-3-((E)-3-oxo-propenyl)-7,8-dihydro-6H-isochromen-7-yl ester 4-Benzyloxy-2-methoxy-6-methyl-benzoic acid (R)-7-methyl-6,8-dioxo-3-((E)-propenyl)-7,8-dihydro-6H-isochromen-7-yl ester (R)-2-(tert-butoxycarbonyl)-6,8-dimethoxy-1,3-dimethyl-1,2-dihydroisoquinoline (R)-6,8-dimethoxy-2-(methoxycarbonyl)-1,3-dimethyl-1,2-dihydroisoquinoline (R,E)-7-hydroxy-7-methyl-3-(prop-1-en-1-yl)-6H-isochromene-6,8(7H)-dione preasperpyranone 7-butyryloxy-5-chloro-3-(3-hydroxypropyl)-7-methyl-6H-isochromene-6,8-dione Isochromophilone VII Isochromophilone III sclerotiorin 7-epi-sclerotiorin 7-episclerotiorin Sclerotiorin