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丙基烯丙基三硫醚 | 33922-73-5

中文名称
丙基烯丙基三硫醚
中文别名
2-烯丙基丙基三硫化物;2-丙烯基三硫丙酯
英文名称
1-allyl-3-propyltrisulfane
英文别名
allyl propyl trisulfide;1-(prop-2-enyltrisulfanyl)propane
丙基烯丙基三硫醚化学式
CAS
33922-73-5
化学式
C6H12S3
mdl
MFCD00085182
分子量
180.359
InChiKey
IXJMGVJLUBBAQW-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

  • LogP:
    3.666 (est)
  • 保留指数:
    1290;1297;1290

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    9
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.666
  • 拓扑面积:
    75.9
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    Acetyl-aethyldisulfidallyl thiotosylatesodium methylate 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 0.18h, 以95%的产率得到丙基烯丙基三硫醚
    参考文献:
    名称:
    Unsymmetrical Organotrisulfide Formation via Low-Temperature Disulfanyl Anion Transfer to an Organothiosulfonate
    摘要:
    New methodology is presented for the formation of unsymmetrical organotrisulfides in a high yield and purity, relatively free of polysulfide byproducts. The highlight of the method is the low-temperature (-78 degrees C) deprotection of a disulfanyl acetate with sodium methoxide in THF to form a disulfanyl anion, which reacts rapidly in situ with an organothiosulfonate (S-aryl or S-alkyl) within 30 seconds followed by quenching. The discovery of these new reaction conditions together with the relative greenness of the chemistry overall makes for an efficient protocol, from which a range of organotrisulfides covering aliphatic, aromatic, as well as cysteine and sugar groups can be accessed in a high yield and purity.
    DOI:
    10.1021/acs.joc.8b03262
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文献信息

  • COMPOSITIONS COMPRISING COENZYME Q-10 AND GARLIC OIL FOR AN INCREASED COENZYME Q-10 BIOAVAILABILITY
    申请人:Cpc (Tianjin) Fine Chemicals Co., Ltd.
    公开号:EP2227229A2
    公开(公告)日:2010-09-15
  • USE OF GARLIC OIL TO INCREASE BIOAVAILABILITY OF COENZYME Q-10
    申请人:Shi Jingang
    公开号:US20090143484A1
    公开(公告)日:2009-06-04
    The invention describes compositions that include a sulfide containing molecule, such a garlic oil, and a coenzyme Q molecule. The sulfide containing molecule solvates the coenzyme Q molecule, thus enhancing the bioavailability of the coenzyme Q molecule in a subject in need thereof, relative to administration of coenzyme Q devoid of the presence of a sulfide containing molecule.
  • [EN] USE OF GARLIC OIL TO INCREASE BIOAVAILABILITY OF COENZYME Q-10<br/>[FR] UTILISATION D'ESSENCE D'AIL POUR AUGMENTER LA BIODISPONIBILITÉ DE LA COENZYME Q-10
    申请人:CPC TIANJIN FINE CHEMICALS CO
    公开号:WO2009073661A2
    公开(公告)日:2009-06-11
    The invention describes compositions that include a sulfide containing molecule, such a garlic oil, and a coenzyme Q molecule. The sulfide containing molecule solvates the coenzyme Q molecule, thus enhancing the bioavailability of the coenzyme Q molecule in a subject in need thereof, relative to administration of coenzyme Q devoid of the presence of a sulfide containing molecule.
  • [EN] COMPOSITIONS COMPRISING COENZYME Q-10 AND GARLIC OIL FOR AN INCREASED COENZYME Q-10 BIOAVAILABILITY<br/>[FR] COMPOSITIONS COMPRENANT LA COENZYME Q-10 ET DE L'ESSENCE D'AIL POUR UNE BIODISPONIBILITÉ ACCRUE DE LA COENZYME Q-10
    申请人:CPC TIANJIN FINE CHEMICALS CO
    公开号:WO2009073659A1
    公开(公告)日:2009-06-11
    The invention describes compositions that include a sulfide containing molecule, such a garlic oil, and a coenzyme Q molecule. The sulfide containing molecule solvates the coenzyme Q molecule, thus enhancing the bioavailability of the coenzyme Q molecule in a subject in need thereof, relative to administration of coenzyme Q devoid of the presence of a sulfide containing molecule.
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同类化合物

香菇素 甲基烯丙基三硫醚 甲基乙基三硫醚 甲基丙基三硫醚 甲基(1-甲基乙基)三硫醚 大蒜粉 双十二烷基三硫醚 二甲基三硫 二甲基-d6三硫醚 二异丙基三硫醚 二叔十二烷基三硫化物 二乙基三硫醚 二丙基三硫醚 二-叔-丁基三硫化物 二(异丙氧基硫代羰基)三硫醚 二(二甲硫基氨基甲酰)三硫醚 二(乙氧基硫代羰基)三硫醚 二(三氯甲基)三硫醚 二(3-羟基丙基)三硫醚 二(2-羟基乙基)三硫醚 二(2-氯乙基)三硫醚 乙基丙基三硫醚 丙基烯丙基三硫醚 三氟-(三氟甲基硫基二硫基)甲烷 N(1),N(3)-二甲基-1,3-三硫烷二硫代甲酰胺 6-肼基-N,N-二(丙-2-烯-1-基)哒嗪-3-胺二盐酸 3,3'-三硫代二丙酰胺 1,1'-三硫代二[N,N-二丁基-硫代甲酰胺] 2-<(1-methyl-2-oxopropyl)trithio>-3-pentanone 3-<(1-methyl-2-oxopropyl)trithio>-2-pentanone 3-<(1-methyl-2-oxobutyl)trithio>-2-pentanone diethyl 4,4'-trithiobis(butanesulfinate) 7-methyl-4,5,6,9,10-pentathiatrideca-1,12-diene 8-methyl-4,5,6,9,10-pentathiatrideca-1,12-diene bis(1-ethyl-2-oxopropyl) trisulfide 1,4,5,6-Oxatrithiocane 2-(2,3,3,4,5,5-Hexamethylhexan-2-yltrisulfanyl)-2,3,3,4,5,5-hexamethylhexane Di-tert-nonyl polysulfide 3,3'-(Ethane-1,2-diyl)bis(N,N-dimethyltrisulfane-1-carbothioamide) O-Ethyl tert-butyltrisulfane-1-carbothioate O-Ethyl butyltrisulfane-1-carbothioate N(1),N(3)-Dibutyl-1,3-trisulfanedicarbothioamide 1,3-Trisulfanedicarbothioamide, N,N'-dicyclohexyl- 1,1'-Trithiobis(N,N-dicyclohexylmethanethioamide di-tert-pentyl trisulfide Dipentylxanthogentrisulfid 4,4,7,7-tetramethyl-1,2,3,5,6-pentathiepane 1-Butanesulfinic acid, 4,4'-trithiobis-, disodium salt 1,2,3,5,6-Pentathiepane, 4,7-dimethyl- Methyl tert-butyltrisulfane-1-carboxylate

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