S-Benzylthiolisobutyrat | 61915-58-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: S-Benzylthiolisobutyrat
• 英文别名: Thio-isobuttersaeure-S-benzylester；S-benzyl thiol-2-methyl-propionate；S-benzyl 2-methylpropanethioate
• CAS: 61915-58-0
• 化学式: C₁₁H₁₄OS
• 分子量: 194.298
• InChiKey: KYJFJIMIPKSVRV-UHFFFAOYSA-N

物化性质

• 沸点：
  274.7±19.0 °C(Predicted)
• 密度：
  1.060±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  13
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  42.4
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  生成 S-Benzylthiolisobutyrat
  参考文献：
  名称：

  Bestmann,H.J.; Saalbaum,H., Bulletin des Societes Chimiques Belges, 1979, vol. 88, p. 951 - 956

  摘要：

  DOI：

文献信息

• Processes for forming amide bonds and compositions related thereto
  申请人：Liebeskind Lanny S.

  公开号：US08921599B2

  公开（公告）日：2014-12-30

  The disclosure relates to methods for producing amide bonds and reagents related thereto. In some embodiments, the disclosure relates to methods of producing an amide comprising mixing an O-silylated thionoester and an amine under conditions such that an amide is formed. In another embodiment, the disclosure relates to mixing a thiolacid, a silylating agent, and an amine under conditions such that an amide is formed.

  该公开涉及生产酰胺键的方法及相关试剂。在某些实施例中，该公开涉及通过混合O-硅烷基硫酸酯和胺在条件下生产酰胺的方法。在另一实施例中，该公开涉及混合硫酸酯、硅基化剂和胺在条件下形成酰胺。
• A novel approach for the direct conversion of alkylsulfonyl derivatives into alkylcarbonyl derivatives via tin-free radical carbonylation
  作者：Sangmo Kim、Kyoung-Chan Lim、Sunggak Kim

  DOI：10.1039/b710939c

  日期：——

  A novel radical approach for the direct conversion of RSO(2)X into RCOX in a single step is devised; the present approach is very simple, highly efficient, and minimizes formation of by-product.

  设计了一种新颖的激进方法，可将RSO（2）X直接转化为RCOX。本方法非常简单，高效并且使副产物的形成最小化。
• Compound embodiments that release H2S by reaction with a reactive compound and methods of making and using the same
  申请人：University of Oregon

  公开号：US11078157B1

  公开（公告）日：2021-08-03

  Disclosed herein are embodiments of a donor compound that releases H2S by reacting with a reactive compound. The donor compound embodiments described herein can be used to deliver H2S to a subject or a sample and further can be used to administer therapeutic agents. The donor compound embodiments also can facilitate bioconjugation. Methods of making and using the donor compound embodiments also are disclosed.

  本文揭示了一种供体化合物的实施例，通过与反应性化合物发生反应释放H2S。本文描述的供体化合物实施例可用于向受试者或样品释放H2S，并且进一步可用于给药治疗剂。供体化合物实施例还可以促进生物共轭。还公开了制备和使用供体化合物实施例的方法。
• Chemical Modification of Proteins
  申请人：Bernardes Goncalo

  公开号：US20110144304A1

  公开（公告）日：2011-06-16

  The invention relates to methods for selectively converting a cysteine residue in a peptide or protein to the dehydroalanine (Dha) residue. The method also works on selenocysteine and substituted cysteine and selenocysteine residues, resulting in the Dha residue which may be converted to any natural or unnatural amino acid residue desired without the alteration of the remainder of the peptide or protein. The invention also allows ligation of a desired peptide at any point rather than at a point where there should be a naturally occurring cysteine, thereby allowing native chemical ligation to be used in the synthesis of peptides that do not contain cysteine. The methodology allows for the synthesis of very large peptides.

  本发明涉及一种将肽或蛋白质中的半胱氨酸残基选择性转化为去氢丙氨酸（Dha）残基的方法。该方法也适用于硒半胱氨酸和取代的半胱氨酸和硒半胱氨酸残基，从而产生Dha残基，该残基可以转化为所需的任何天然或非天然氨基酸残基，而不改变肽或蛋白质的其余部分。本发明还允许在任何点上连接所需的肽，而不是在应该存在天然半胱氨酸的点上进行连接，从而允许在合成不含半胱氨酸的肽时使用天然化学连接。该方法允许合成非常大的肽。
• BESTMANN H. J.; SAALBAUM H., BULL. SOC. CHIM. BELG., 1959, 88, NO 11, 951-956
  作者：BESTMANN H. J.、 SAALBAUM H.

  DOI：——

  日期：——