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2-propyl 2-propanesulfonate ester | 27907-12-6

中文名称
——
中文别名
——
英文名称
2-propyl 2-propanesulfonate ester
英文别名
2-Propyl-2-Propansulfonat;isopropyl isopropanesulfonate;Propan-2-yl propane-2-sulfonate
2-propyl 2-propanesulfonate ester化学式
CAS
27907-12-6
化学式
C6H14O3S
mdl
——
分子量
166.241
InChiKey
BKQKVXFDAZBBFX-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):
    1.2
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    51.8
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-propyl 2-propanesulfonate ester三正丁基氢锡 作用下, 以 various solvent(s) 为溶剂, 生成 Isopropylsulfonyl-Radikal
    参考文献:
    名称:
    Generation of sulphonyl radicals from sulphonate esters
    摘要:
    DOI:
    10.1016/s0040-4039(00)97388-x
  • 作为产物:
    描述:
    2-propanesulfonyl-1-d chloride 、 异丙醇三乙胺 作用下, 以 二氯甲烷 为溶剂, 生成 2-propyl 2-propanesulfonate ester
    参考文献:
    名称:
    Organic sulfur mechanisms. 36. Cyclopropanesulfonyl chloride: its mechanisms of hydrolysis and reactions with tertiary amines in organic media
    摘要:
    Cyclopropanesulfonyl chloride (1) has been synthesized and its reactions examined to see if the three-membered ring leads to unusual reactions in either 1 or the corresponding sulfene, cyclopropanethione S,S-dioxide (2). pH-rate profiles, primary kinetic isotope effects (KIE's), and pH-product ratio experiments are in full agreement with mechanisms of hydrolysis of 1 like those of a simple alkanesulfonyl chlorides (J. Am. Chem. Soc. 1992,114,1743-1749), specifically, (a) below pH 7.2 by S(N)2-S reaction with water and (b) above pH 7.3, elimination by hydroxide to form the sulfene (2) which is trapped by (i) water below pH 12.0 and (ii) hydroxide above pH 12.0. The products of the reaction of cyclopropanesulfonyl-1-d chloride (9) with triethylamine and 2-propanol in dichloromethane indicate that most of the reaction goes via 2; the analogous reaction with trimethylamine apparently proceeds by a direct formation of the sulfonylammonium chloride (14) which then yields the alpha-deuterated N,N-dimethyl sulfonamide (12, R = Me). The evident sulfene formation processes in the reaction of triethylamine with ethanesulfonyl, 2-propanesulfonyl, and cyclopropanesulfonyl chlorides show very low primary KIE's (<1.5), pointing to highly product-like transition states. Reaction of 1 with an enamine (1-pyrrolidino-2-methylpropene, 20) in the presence of a base in either water or dichloromethane gave cyclopropanesulfonpyrrolidide (23) and an aldehyde adduct (24), but no four-membered cycloadduct (21).
    DOI:
    10.1021/jo00057a027
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文献信息

  • Surfactant-Enabled Transition Metal-Catalyzed Chemistry
    申请人:Berl Volker
    公开号:US20110130562A1
    公开(公告)日:2011-06-02
    In one embodiment, the present application discloses mixtures comprising (a) water in an amount of at least 1% wt/wt of the mixture; (b) a transition metal catalyst; and (c) one or more solubilizing agents; and methods for using such mixtures for performing transition metal mediated bond formation reactions.
    本申请公开了一种组合物,包括(a)至少占组合物总重量1%的水;(b)过渡金属催化剂;以及(c)一种或多种增溶剂;以及使用该组合物进行过渡金属介导的键形成反应的方法。
  • Vitamin-Receptor Binding Drug Delivery Conjugates
    申请人:Endocyte, Inc.
    公开号:US20160220694A1
    公开(公告)日:2016-08-04
    The invention describes a vitamin receptor binding drug delivery conjugate, and preparations therefor. The drug delivery conjugate consists of a vitamin receptor binding moiety, a bivalent linker (L), and a drug. The vitamin receptor binding moiety includes vitamins, and vitamin receptor binding analogs and derivatives thereof, and the drug includes analogs and derivatives thereof. The vitamin receptor binding moiety is covalently linked to the bivalent linker, and the drug, or the analog or the derivative thereof, is covalently linked to the bivalent linker, wherein the bivalent linker (L) includes components such as spacer linkers, releasable linkers, and heteroatom linkers, and combinations thereof. Methods and pharmaceutical compositions for eliminating pathogenic cell populations using the drug delivery conjugate are also described.
    该发明描述了一种维生素受体结合药物传递共轭物及其制备方法。药物传递共轭物由维生素受体结合基团、双价连接剂(L)和药物组成。维生素受体结合基团包括维生素、维生素受体结合类似物及其衍生物,药物包括类似物及其衍生物。维生素受体结合基团与双价连接剂共价连接,药物或其类似物或衍生物与双价连接剂共价连接,其中双价连接剂(L)包括间隔连接剂、可释放连接剂和杂原子连接剂以及其组合。还描述了利用该药物传递共轭物消除病原细胞群的方法和药物组合物。
  • COMPOUNDS HAVING MUSCARINIC RECEPTOR ANTAGONIST AND BETA2 ADRENERGIC RECEPTOR AGONIST ACTIVITY
    申请人:Rancati Fabio
    公开号:US20130045169A1
    公开(公告)日:2013-02-21
    Compounds of formula (I) act both as muscarinic receptor antagonists and beta2 adrenergic receptor agonists and are useful for the prevention and/or treatment of broncho-obstructive and inflammatory diseases.
    式(I)的化合物既作为肌动蛋白受体拮抗剂,又作为β2肾上腺素受体激动剂,可用于预防和/或治疗支气管阻塞性和炎症性疾病。
  • .alpha.-Alkylation of alkyl alkanesulfonates
    作者:William E. Truce、D. J. Vrencur
    DOI:10.1021/jo00829a097
    日期:1970.4
  • CULSHAW, PETER N.;WALTON, JOHN C., TETRAHEDRON LETT., 31,(1990) N7, C. 2457-2460
    作者:CULSHAW, PETER N.、WALTON, JOHN C.
    DOI:——
    日期:——
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