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2-tert-butyl-1,3-oxathiolane | 17643-69-5

中文名称
——
中文别名
——
英文名称
2-tert-butyl-1,3-oxathiolane
英文别名
2-tert.-Butyl-1,3-oxathiolan;1,3-Oxathiolane, 2-(1,1-dimethylethyl)-
2-tert-butyl-1,3-oxathiolane化学式
CAS
17643-69-5
化学式
C7H14OS
mdl
——
分子量
146.254
InChiKey
MWSYUUWTKSTCAI-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:
    197.0±33.0 °C(Predicted)
  • 密度:
    1.005±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    34.5
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:e5ab94b96da7f0b80774eae61ef4ae08
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反应信息

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文献信息

  • A ring expansion reaction of 1,3-oxathiolanes
    作者:Maria Ioannou、Michael J. Porter、Fabienne Saez
    DOI:10.1039/b110754b
    日期:2002.2.12
    1,3-Oxathiolanes are efficiently converted, via sulfur ylide intermediates, to 1,4-oxathianes by ring expansion with a silylated diazoacetate in the presence of a copper catalyst.
    在铜催化剂的作用下,1,3-氧硫杂环戊烷通过硫酰亚胺中间体与硅烷化重氮乙酸酯发生扩环反应,从而高效地转化为 1,4-氧硫杂环戊烷。
  • Conversion of 1,3-oxathiolanes to 1,4-oxathianes using a silylated diazoester
    作者:Maria Ioannou、Michael J. Porter、Fabienne Saez
    DOI:10.1016/j.tet.2004.10.063
    日期:2005.1
    Treatment of substituted 1,3-oxathiolanes with ethyl (triethylsilyl)diazoacetate in the presence of a copper catalyst effects one-carbon ring expansion to the corresponding 3-triethylsilyl-1,4-oxathiane-3-carboxylates. Subsequent desilylation can be brought about by treatment with tetrabutyl ammonium fluoride. (C) 2004 Elsevier Ltd. All rights reserved.
  • Topical Compositions Comprising Non-Proteogenic Amino Acids and Methods of Treating Skin
    申请人:Ptchelintsev Dmitri S.
    公开号:US20100261769A1
    公开(公告)日:2010-10-14
    Cosmetic compositions comprising non-natural, non-proteogenic amino acids and methods of using such compositions to impart antiaging benefits to the skin are disclosed. The non-natural, non-proteogenic amino acids are believed to have modulatory activity against one or more biochemical pathways implicated in skin aging, and in particular, are enhancers of LOXL-1.
  • Paxillin Stimulating Compositions and Cosmetic Uses Thereof
    申请人:ZHENG Qian
    公开号:US20110151029A1
    公开(公告)日:2011-06-23
    Cosmetic compositions comprising one or more paxillin stimulators and methods of using such compositions to impart anti-aging benefits to the skin are disclosed. The paxillin stimulators and combinations thereof are believed to have modulatory activity against at least one biochemical pathway implicated in skin aging.
  • TYROSINASE INHIBITORS
    申请人:AVON PRODUCTS, INC.
    公开号:US20150164758A1
    公开(公告)日:2015-06-18
    The compositions and methods of described herein comprise novel ingredients effective to reduce unwanted pigmentation, such as skin discoloration, freckles, age spots, liver spots, sun damage, tans, pigmented acne marks, scars, pigmented birthmarks, hyperpigmentation, post-inflammatory hyperpigmentation, post-injury hyperpigmentation, melasma, cholasma, after-burn scar, nail stain, yellowing of skin, dark circles under eyes, and the like. The composition may include additional ingredients accordingly for a colored cosmetic, moisturizer, cleanser, toner, and the like.
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同类化合物

顺式-1,3-氧硫杂环戊烷-4-酮O-((甲基氨基)羰基)肟 甲基1,3-恶噻戊环-2-羧酸酯 反-2-顺式-4,5-三甲基-1,3-恶噻戊环 三甲基-[[(2S,5S)-2-甲基-3-氧代-1,3-氧硫杂环戊烷-5-基]甲基]铵碘化物 三甲基-[(2-甲基-1,3-氧硫杂环戊烷-5-基)甲基]铵 beta-磺基丙酸酐 5-羟基-1,3-噁硫杂烷-2-羧酸 5-甲基恶噻戊环2,2-二氧化物 5-(氯甲基)-1,3-恶噻戊环-2-硫酮 5-(异丁烯酰氧基)甲基-1,3-氧硫杂环戊烷-2-硫酮 4-甲基-1,2-噁噻戊环2,2-二氧化 4-溴-[1,2]噁硫烷2,2-二氧化物 4,5-二甲基-2-[2-(甲硫基)乙基]-1,3-恶噻戊环 3-苄基-1,2-氧硫杂环戊烷2,2-二氧化物 3-氟-1,3-丙烷磺酸内酯 3-十三烷基-1,3-丙烷磺内酯 2-甲基-5-三甲基铵甲基-1,3-恶噻戊环 2-甲基-1,3-恶噻戊环 2-异丙基-1,3-恶噻戊环 2-亚氨基-1,3-恶噻戊环-4-羧酸 2-(2,6-二甲基-1,5-庚二烯-1-基)-1,3-恶噻戊环 2,4-丁磺内酯 2,4,4,5,5-五氟-2-(三氟甲基)-1,3-恶噻戊环3,3-二氧化物 1-巯基十四烷-3-醇 1-[(2Z)-1,3-氧硫杂环戊烷-2-亚基]脲 1-(1,3-氧硫杂环戊烷-2-基)乙酮 1,3-氧硫杂环戊烷-5-酮 1,3-氧硫杂环戊烷-2-酮 1,3-恶噻戊环 1,3-丙烷磺内酯 (Z)-5-丙基-1,3-氧硫杂环戊烷-4-酮O-((甲基氨基)羰基)肟 3,4-dimethyl-1,2-oxathiolane-5-one-2,2-dioxide 5,5-dimethyl-1,3-oxathiolan-2-one 2-(5-methyl-furan-2-yl)-[1,3]oxathiolane 5,5-dimethyl-4-(2-yne butylidene)-2-thione-1,3-oxathiolane N-(1-adamantyl)-1,3-oxathiolan-2-imine 5-ethyl-1,3-oxathiolane-2-thione 2,2,4,4,5,5-hexafluoro[1,3]oxathiolane-3,3-dioxide 4,4,5,5-tetramethyl-1,3-oxathiolane-2-thione 3-phenyl-3a,6a-dihydro-6H-[1,2]oxathiolo[3,4-d]isoxazole 4,4-dioxide 2-[1-methylbutenyl]-1,3-oxathiolane 2-trifluoromethyl-1,3-oxathiolan-5-one 2-butylidene-5-methyl-1,3-oxathiolane N-(tert-butyl)-5-methyl-1,3-oxathiolan-2-imine 5-(allyloxymethyl)-1,3-oxathiolane hexahydrobenzo[d][1,3]oxathiole 5-ethyl-1,3-oxathiolane (+/-)-5,6-dimethyl-3a,4,7,7a-tetrahydro-2,1-oxathiaindene 1,1-dioxide 2-(thiophen-2-yl)-1,3-oxathiolane 2-Undecyl-1,3-oxathiolane