1-(2-tert-butylsulfanyl-1-chloroethyl)-4-methoxybenzene | 628298-08-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 1-(2-tert-butylsulfanyl-1-chloroethyl)-4-methoxybenzene
• CAS: 628298-08-8
• 化学式: C₁₃H₁₉ClOS
• 分子量: 258.812
• InChiKey: VYIJPEDJMDYGPQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  16
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  34.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-(2-tert-butylsulfanyl-1-chloroethyl)-4-methoxybenzene 在 sodium hydroxide 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 为溶剂， 反应 10.0h， 生成 [2-tert-butylsulfanyl-1-(4-methoxyphenyl)ethylamino]acetic acid hydrochloride
  参考文献：
  名称：

  Derivatized Amino Acids Relevant to Native Peptide Synthesis by Chemical Ligation and Acyl Transfer

  摘要：

  Three amino acids were converted into the derivatives 5.2 (from glycine), 6.4a and 6.4b (from alanine), and 8.3a and 8.3b (from O-benzyl serine). These N-alkylated amino acids, which can be deprotected after conversion of the carboxyl into an amide, correspond to the general structure 2.1, a compound class of use in the study of peptide segment coupling by the ligation-acyl transfer method.

  DOI：

  10.1021/jo030192r
• 作为产物：
  描述：

  2-tert-butylsulfanyl-1-(4-methoxyphenyl)ethanone 在 sodium tetrahydroborate 、 氯化亚砜 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 2.0h， 生成 1-(2-tert-butylsulfanyl-1-chloroethyl)-4-methoxybenzene
  参考文献：
  名称：

  Derivatized Amino Acids Relevant to Native Peptide Synthesis by Chemical Ligation and Acyl Transfer

  摘要：

  Three amino acids were converted into the derivatives 5.2 (from glycine), 6.4a and 6.4b (from alanine), and 8.3a and 8.3b (from O-benzyl serine). These N-alkylated amino acids, which can be deprotected after conversion of the carboxyl into an amide, correspond to the general structure 2.1, a compound class of use in the study of peptide segment coupling by the ligation-acyl transfer method.

  DOI：

  10.1021/jo030192r

文献信息

• Derivatized Amino Acids Relevant to Native Peptide Synthesis by Chemical Ligation and Acyl Transfer
  作者：Derrick L. J. Clive、Soleiman Hisaindee、Don M. Coltart

  DOI：10.1021/jo030192r

  日期：2003.11.1

  Three amino acids were converted into the derivatives 5.2 (from glycine), 6.4a and 6.4b (from alanine), and 8.3a and 8.3b (from O-benzyl serine). These N-alkylated amino acids, which can be deprotected after conversion of the carboxyl into an amide, correspond to the general structure 2.1, a compound class of use in the study of peptide segment coupling by the ligation-acyl transfer method.