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aerugine | 118491-87-5

中文名称
——
中文别名
——
英文名称
aerugine
英文别名
2-[4-(Hydroxymethyl)-4,5-dihydro-1,3-thiazol-2-yl]phenol;2-[4-(hydroxymethyl)-4,5-dihydro-1,3-thiazol-2-yl]phenol
aerugine化学式
CAS
118491-87-5
化学式
C10H11NO2S
mdl
——
分子量
209.269
InChiKey
CQCVSXXDUMTFCR-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
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    78.1
  • 氢给体数:
    2
  • 氢受体数:
    4

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:
    aerugine草酰氯二甲基亚砜三乙胺 作用下, 生成 2-(2-Hydroxyphenyl)thiazole-4-carboxaldehyde
    参考文献:
    名称:
    Stereochemical Assignment of the Pyochelins
    摘要:
    The synthesis of pyochelin has been much improved but gives four stereoisomers. The stereochemistry of the two naturally occurring pyochelins I and II has been assigned, based on (1) the similarity of the NMR spectra of pyochelin I methyl ester to those for 4-methylpyochelin I methyl ester, whose X-ray structure has been determined and relative stereochemistry assigned; (2) comparison of the rotation of the natural material to that of pyochelin I methyl ester synthesized from N-methyl-L-cysteine methyl ester, which is not expected to epimerize during the synthesis and thus assigns pyochelin I methyl ester as 4'R,2 '' R,4 '' R; and (3) the known facile epimerization at C-2 '' of 2 ''-substituted thiazolidine-4-carboxylic acids, which assigns the other (unfavored) naturally occurring isomer, pyochelin II, as 4'R,2 '' S,4 '' R. The remaining two synthetic products, neopyochelin I methyl ester and neopyochelin II methyl ester, were assigned the stereochemistry 4'S,2 '' S,4 '' R and 4'S,2 '' R,4 '' R, respectively, based on (1) the use of N-methyl-L-cysteine methyl ester in their synthesis, which establishes C-4 '' as R; (2) the known instability at C-2 '', which favors neopyochelin II (2 '' R) over neopyochelin I (2 '' S); and (3) the requirement of nonidentity with pyochelins I and II, which requires the S configuration at C-4'.
    DOI:
    10.1021/jo00114a029
  • 作为产物:
    描述:
    邻羟基苯甲腈 在 sodium tetrahydroborate 、 lithium aluminium tetrahydride 、 potassium carbonate盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺N,N-二异丙基乙胺 作用下, 以 甲醇 、 aq. phosphate buffer 、 乙醚二氯甲烷 为溶剂, 反应 25.17h, 生成 aerugine
    参考文献:
    名称:
    聚合的古铁青霉素为Ga 3+配合物的全合成
    摘要:
    含铁细胞piscibactin是参与致病细菌的铁摄取的主要毒力因子发光菌damselae亚种。piscicida和Anguillarum弧菌分别负责鱼类细菌光致细菌(巴氏杆菌病)和弧菌病。描述了使用l- / d-半胱氨酸作为手性试剂和梅德鲁姆酸的Ga 3+络合物的收敛全合成。酸敏感的β-羟基-2,4-二取代的噻唑啉部分和方便的保护基团的合成中的Staudinger还原/ Aza-Wittig工艺是该合成的关键步骤。
    DOI:
    10.1021/acs.orglett.0c03850
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文献信息

  • Thiazoline‐Iridium (III) Complexes and Immobilized Nanomaterials as Selective Catalysts in <i>N</i> ‐Alkylation of Amines with Alcohols
    作者:Serpil Denizaltı、Serkan Dayan、Salih Günnaz、Ertan Şahin
    DOI:10.1002/aoc.5970
    日期:2020.12
    thiazoline‐iridium (III) complexes (4–7) derived from cysteine were prepared and fully characterized by conventional methods. The molecular structure of complex 5 was also determined by single‐crystal X‐ray diffraction. These complexes were evaluated as catalysts for hydrogen‐borrowing reactions of amines with alcohols. In particular, complex 5 showed the best activity as catalyst. Various amines have
    在这项研究中,一个新的系列噻唑啉的铱(III)配合物(4 - 7)来自半胱氨酸制备并通过常规方法充分表征。配合物5的分子结构也通过单晶X射线衍射确定。这些络合物被评估为胺与醇的氢借位反应的催化剂。特别地,配合物5显示出作为催化剂的最佳活性。各种胺已被醇烷基化,可提供中等至良好的收率(33–99%)。此外,采用最佳催化剂5进行超声处理,制备了固定化的纳米材料(M 1,2)。分别使用多壁碳纳米管(MWCNT)和氧化石墨烯(GO),并通过X射线衍射(XRD),傅里叶变换红外(FT-IR)光谱,场发射扫描电子显微镜(FE-SEM)进行表征,能量色散X射线(EDX)光谱和电感耦合等离子体质谱(ICP-MS)。的中号1,2纳米材料也进行了测试,如用于模型催化反应的催化剂Ñ烷基化。的中号1的纳米材料显示出比显著更高的活性中号2纳米材料。的中号1催化剂通过过滤回收并用于与高转化率4个催化循环(99%,97%,96%,和86%)再利用。
  • METHODS AND COMPOSITIONS RELATED TO NEUROACTIVE THIAZOLINE COMPOUNDS
    申请人:Schmidt Eric W.
    公开号:US20140018400A1
    公开(公告)日:2014-01-16
    In one aspect, the invention relates to compounds having a general structure: and methods of using same to modulate calcium release. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    在某个方面,本发明涉及具有一般结构的化合物:以及使用同样的方法来调节钙释放。本摘要旨在作为扫描工具,用于在特定技术领域进行搜索,不旨在限制本发明。
  • Structure of aerugine from Pseudomonas aeruginosa
    作者:A. Zunnundzhanov、I. A. Bessonova、N. D. Abdullaev、D. K. Ogai
    DOI:10.1007/bf00597805
    日期:1987.7
  • Identification of the bacterial metabolite aerugine as potential trigger of human dopaminergic neurodegeneration
    作者:Anna-Katharina Ückert、Sina Rütschlin、Simon Gutbier、Nathalie Christine Wörz、Mahfuzur R. Miah、Airton C. Martins、Isa Hauer、Anna-Katharina Holzer、Birthe Meyburg、Ann-Kathrin Mix、Christof Hauck、Michael Aschner、Thomas Böttcher、Marcel Leist
    DOI:10.1016/j.envint.2023.108229
    日期:2023.10
  • US9751847B2
    申请人:——
    公开号:US9751847B2
    公开(公告)日:2017-09-05
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