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N-acetylbenzothiazoline-2-thione | 660390-61-4

中文名称
——
中文别名
——
英文名称
N-acetylbenzothiazoline-2-thione
英文别名
3-acetyl-3H-benzothiazole-2-thione;1-(2-Sulfanylidene-1,3-benzothiazol-3-yl)ethanone
N-acetylbenzothiazoline-2-thione化学式
CAS
660390-61-4
化学式
C9H7NOS2
mdl
——
分子量
209.293
InChiKey
XEJIXGQBELKQTG-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:
    350.0±25.0 °C(Predicted)
  • 密度:
    1.46±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    77.7
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:9cc8901066f25c999bba06eb4dc7031e
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上下游信息

  • 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:
    N-acetylbenzothiazoline-2-thione三乙胺 作用下, 以 氘代氯仿二氯甲烷 为溶剂, 反应 6.0h, 生成 N-(iso-butyryl)benzothiazoline-2-thione
    参考文献:
    名称:
    Acylation and Alkoxycarbony-lation of Benzoxazoline-2-thione and Benzothiazoline-2-thione
    摘要:
    Acylation of benzoxazoline-2-thione (1) and benzothiazoline-2-thione (2) with acetic anhydride (3) and acyl chlorides (4) gave N-acyl (5, 6) and/or S-acyl (7, 8) derivatives depending on the nature of acylating agents and bases used. Alkoxycarbonylation of 1 with aralkyl chlorocarbonates (9) gave N-alkoxycarbonyl derivatives (10) mainly, while that of 2 with aralkyl chloroccarbonates (9) gave S-alkoxycarbonyl derivatives (12) exclusively. Photolysis of N-acyl derivatives (5 or 6) in the presence of alcohols afforded 1 or 2, respectively, together with esters (16).
    DOI:
    10.3987/com-03-s(p)10
  • 作为产物:
    参考文献:
    名称:
    Michael and Mannich reactions with benzothiazole-2-thiol
    摘要:
    DOI:
    10.1021/jo00804a006
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文献信息

  • Eight-arm polyethylene glycol derivative, production method therefor, and modified bio-related substance thereof
    申请人:XIAMEN SINOPEG BIOTECH CO., LTD.
    公开号:US10434182B2
    公开(公告)日:2019-10-08
    Disclosed are an eight-arm polyethylene glycol (PEG) derivative (formula I), production method therefor and modified bio-related substance thereby. Wherein, one tetravalent group U together with four trivalent groups Ec form a highly symmetrical octavalent group CORE0; Lc connects the octavalent group to eight PEG chains having polydispersity or monodispersity and having n1 to n8 as the degree of polymerization thereof; the terminal of one PEG chain is connected to at least one functional group F (k≥1); said PEG chain and F therebetween can be directly connected (g=0) or be indirectly connected via a linking group L0 to a terminal end-branching group G (g=1); the latter provides more reactive sites for binding more drug molecules and increases the drug loading. The eight-arm polyethylene glycol derivative has a centrosymmetric or approximately centrosymmetric structure, and leads to more precise control of the molecular weight in large-scale production and much narrower distribution of molecular weight for products. The modified bio-related substance thereby has a more uniform and controllable performance.
    本发明公开了一种八臂聚乙二醇(PEG)衍生物(式 I)、其生产方法及其改性生物相关物质。其中,一个四价基团 U 与四个三价基团 Ec 形成一个高度对称的八价基团 CORE0;Lc 将八价基团连接到八条具有多分散性或单分散性且聚合度为 n1 至 n8 的 PEG 链上;一条 PEG 链的末端与至少一个官能团 F 连接(k≥1);所述 PEG 链和 F 之间可以直接连接(g=0),也可以通过连接基团 L0 与末端支化基团 G 间接连接(g=1);后者提供了更多的反应位点,可以结合更多的药物分子,增加药物负载量。八臂聚乙二醇衍生物具有中心对称或近似中心对称结构,因此在大规模生产中可以更精确地控制分子量,产品的分子量分布也更窄。因此,改性生物相关物质的性能更均匀、更可控。
  • Multifunctionalized polyethylene glycol derivative and preparation method therefor
    申请人:XIAMEN SINOPEG BIOTECH CO., LTD.
    公开号:US11324827B2
    公开(公告)日:2022-05-10
    Disclosed are a multifunctionalized polyethylene glycol derivative and a preparation method therefor. The derivative has an H-shaped structure as represented by formula (1) and comprises one linear core LPEG and four PEG branch chains, where n1, n2, n3, and n4 respectively are the degrees of polymerization of the branch chains, U1 and U2 are trivalent branching groups connecting the core LPEG to two of the PEG branch chains, F1 and F2 contain a functional group or a protected form R01 thereof and may or may not contain a branched group G, correspondingly, the number of R01 is one or more, F1 and F2 are either identical or different, any one linking group in the molecule or any linking group formed with an adjacent heteroatom group can either remain stable or be degraded, and any one PEG segment in the molecule is discretely polydispersed or monodispersed. The multifunctional polyethylene glycol is flexible and diverse in terms of branch structures and the lengths of branching arms, has various parameters and performance indicators that are adjustable and easy to control, and has a broad applicability.
    本发明公开了一种多功能聚乙二醇衍生物及其制备方法。该衍生物具有由式(1)表示的 H 型结构,包括一个线性核心 LPEG 和四个 PEG 支链,其中 n1、n2、n3 和 n4 分别为支链的聚合度,U1 和 U2 为连接核心 LPEG 和两个 PEG 支链的三价支化基团、F1 和 F2 含有一个官能团或其保护形式 R01,可以含有或不含有支链基团 G,相应地,R01 的数目为一个或多个,F1 和 F2 要么相同要么不同,分子中的任何一个连接基团或与相邻杂原子基团形成的任何连接基团要么保持稳定,要么降解,分子中的任何一个 PEG 段离散多分散或单分散。多功能聚乙二醇的支链结构和支臂长度灵活多样,各种参数和性能指标可调且易于控制,具有广泛的适用性。
  • MULTIFUNCTIONALIZED POLYETHYLENE GLYCOL DERIVATIVE AND PREPARATION METHOD THEREFOR
    申请人:XIAMEN SINOPEG BIOTECH CO., LTD.
    公开号:US20170312363A1
    公开(公告)日:2017-11-02
    Disclosed are a multifunctionalized polyethylene glycol derivative and a preparation method therefor. The derivative has an H-shaped structure as represented by formula (1) and comprises one linear core LPEG and four PEG branch chains, where n 1 , n 2 , n 3 , and n 4 respectively are the degrees of polymerization of the branch chains, U 1 and U 2 are trivalent branching groups connecting the core LPEG to two of the PEG branch chains, F 1 and F 2 contain a functional group or a protected form R 01 thereof and may or may not contain a branched group G, correspondingly, the number of R 01 is one or more, F 1 and F 2 are either identical or different, any one linking group in the molecule or any linking group formed with an adjacent heteroatom group can either remain stable or be degraded, and any one PEG segment in the molecule is discretely polydispersed or monodispersed. The multifunctional polyethylene glycol is flexible and diverse in terms of branch structures and the lengths of branching arms, has various parameters and performance indicators that are adjustable and easy to control, and has a broad applicability.
  • EIGHT-ARM POLYETHYLENE GLYCOL DERIVATIVE, PRODUCTION METHOD THEREFOR, AND MODIFIEDBIO-RELATEDSUBSTANCETHEREOF
    申请人:XIAMEN SINOPEG BIOTECH CO., LTD
    公开号:US20180214561A1
    公开(公告)日:2018-08-02
    Disclosed are an eight-arm polyethylene glycol (PEG) derivative (formula I), production method therefor and modified bio-related substance thereby. Wherein, one tetravalent group U together with four trivalent groups E c form a highly symmetrical octavalent group CORE 0 ; L c connects the octavalent group to eight PEG chains having polydispersity or monodispersity and having n 1 to n 8 as the degree of polymerization thereof; the terminal of one PEG chain is connected to at least one functional group F (k≥1); said PEG chain and F therebetween can be directly connected (g=0) or be indirectly connected via a linking group L 0 to a terminal end-branching group G (g=1); the latter provides more reactive sites for binding more drug molecules and increases the drug loading. The eight-arm polyethylene glycol derivative has a centrosymmetric or approximately centrosymmetric structure, and leads to more precise control of the molecular weight in large-scale production and much narrower distribution of molecular weight for products. The modified bio-related substance thereby has a more uniform and controllable performance.
  • Acylation and Alkoxycarbony-lation of Benzoxazoline-2-thione and Benzothiazoline-2-thione
    作者:Takehiko Nishio、Kiyoko Shiwa
    DOI:10.3987/com-03-s(p)10
    日期:——
    Acylation of benzoxazoline-2-thione (1) and benzothiazoline-2-thione (2) with acetic anhydride (3) and acyl chlorides (4) gave N-acyl (5, 6) and/or S-acyl (7, 8) derivatives depending on the nature of acylating agents and bases used. Alkoxycarbonylation of 1 with aralkyl chlorocarbonates (9) gave N-alkoxycarbonyl derivatives (10) mainly, while that of 2 with aralkyl chloroccarbonates (9) gave S-alkoxycarbonyl derivatives (12) exclusively. Photolysis of N-acyl derivatives (5 or 6) in the presence of alcohols afforded 1 or 2, respectively, together with esters (16).
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