摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(Z)-甲基苯基二氮烯 | 34000-44-7

中文名称
(Z)-甲基苯基二氮烯
中文别名
——
英文名称
(Z)-Methylphenyldiazen
英文别名
cis-Phenylazomethan;syn-Methylphenyldiimid
(Z)-甲基苯基二氮烯化学式
CAS
34000-44-7
化学式
C7H8N2
mdl
——
分子量
120.154
InChiKey
SHHIUWFOBYRJAM-HJWRWDBZSA-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:
    156.6±9.0 °C(Predicted)
  • 密度:
    0.96±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    9.0
  • 可旋转键数:
    1.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    24.72
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为产物:
    描述:
    1-acetyl-1-methyl-2-phenylhydrazine 在 phosphate buffer 、 potassium hexacyanoferrate(III) 作用下, 以 为溶剂, 反应 2.0h, 以35.5%的产率得到(Z)-甲基苯基二氮烯
    参考文献:
    名称:
    Bresser; Weber, Pharmazie, 1996, vol. 51, # 7, p. 470 - 476
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • [EN] FUNCTIONALIZED AND MULTIVARIATE BTB-BASED METAL ORGANIC FRAMEWORKS<br/>[FR] STRUCTURES DE SQUELETTES ORGANOMÉTALLIQUES À BASE DE BTB À PLUSIEURS VARIABLES ET FONCTIONNALISÉS
    申请人:UNIV CALIFORNIA
    公开号:WO2015157239A1
    公开(公告)日:2015-10-15
    The disclosure provides for metal organic frameworks (MOFs) which comprise a plurality of SBUs linked together by functionalized or multivariate BTB-based linking ligands. The disclosure further provides for the use of these MOFs in variety of applications, including for gas separation, gas storage, catalysis, and separation of compounds or bioproducts.
    该披露提供了一种属有机框架(MOFs),其包括通过功能化或多元BTB基连接配体连接在一起的多个SBUs。该披露进一步提供了这些MOFs在各种应用中的使用,包括用于气体分离、气体储存、催化和化合物或生物产品的分离。
  • Detecting targets using mass tags and mass spectrometry
    申请人:Ventana Medical Systems, Inc.
    公开号:US10883999B2
    公开(公告)日:2021-01-05
    Particular disclosed embodiments disclosed herein concern using a one or more various mass tags, which can be specifically deposited at targets through direct or indirect enzymatic-catalyzed transformation, to provide a method for identifying targets in tissue samples. The mass tags may be labeled with stable isotopes to produce mass tags having the same chemical structure but different masses. Mass codes produced by ionizing the mass tags are detected and/or quantified using mass spectrometry. The method can be used for multiplexed detection of multiple targets in a particular sample. In some embodiments, a map divided into sections representing sections of the tissue sample may be prepared, with the map sections including data corresponding to quantification data wherein the size of a mass peak is determined and correlated with the amount of a target for the corresponding tissue sample section.
    本文所公开的具体实施方案涉及使用一种或多种不同的质量标记,通过直接或间接的酶催化转化特异性地沉积在靶标上,从而提供一种识别组织样本中靶标的方法。质量标签可以用稳定同位素标记,以产生化学结构相同但质量不同的质量标签。通过电离质量标签产生的质量代码可使用质谱法进行检测和/或定量。该方法可用于特定样品中多个目标的多重检测。在某些实施方案中,可制备代表组织样本切片的图谱,图谱切片包括与定量数据相对应的数据,其中质量峰的大小被确定并与相应组织样本切片的靶标量相关联。
  • Reactive navy to black dye composition and dye product thereof
    申请人:Zhejiang Keyong Chemical Co., Ltd.
    公开号:US10954392B2
    公开(公告)日:2021-03-23
    A reactive navy to black dye composition comprises component A and component B, wherein component A is selected from one or more compounds of formula (I), component B is selected from one or more compounds of formula (II); D1 and D2 are each independently a group represented by the following formula (a) or (b) or (c); R1-R12 are each independently selected from the group consisting of H, linear or branched C1˜C4 alkyl, C1˜C4 alkoxy and sulfo; m, n=0-3, and every R3 is each independently selected from the group consisting of amino, sulfo, ureido, C1˜C4 alkanoylamino, C1˜C4 alkoxy and C1˜C4 alkyl, every R6 is each independently selected from the group consisting of amino, hydroxyl and sulfo; X1-X3 are each independently selected from the group consisting of H, C1˜C4 alkyl, C1˜C4 alkoxy, —SO2Y1, —NHCO(CH2)pSO2Y2 and —CONH(CH2)qSO2Y3, and at least one of D1 and D2 contains a fiber-reactive group, p, q=1-3, and Y1˜Y5 are each independently selected from the group consisting of —CH═CH2, —C2H4OSO3H and —CH2CH2Cl. A reactive navy to black dye product comprising the dye composition, has the properties of good washing fastness, high degree of fixation and dye-uptake, good build-up, clear remanent dyeing liquor, and the like.
    一种活性海军蓝至黑色染料组合物包括组分A和组分B,其中组分A选自式(I)的一种或多种化合物,组分B选自式(II)的一种或多种化合物;D1和D2各自独立地为下式(a)或(b)或(c)所代表的基团;R1-R12各自独立地选自H、线性或支链C1˜C4烷基、C1˜C4烷氧基和磺基组成的组;m、n=0-3 和每个 R3 各自独立地选自由基、磺基、基、C1˜C4 烷酰基、C1˜C4 烷氧基和 C1˜C4 烷基组成的组,每个 R6 各自独立地选自由基、羟基和磺基组成的组;X1-X3 各自独立地选自由 H、C1˜C4 烷基、C1˜C4 烷氧基、-SO2Y1、-NHCO(CH2)pSO2Y2 和-CONH( )qSO2Y3 组成的组,且 D1 和 D2 中至少有一个含有纤维活性基团,p、q=1-3,以及 Y1˜Y5 各自独立地选自由 -CH═ 、-C2H4OSO3H 和 - Cl 组成的组。包含该染料组合物的活性海军蓝至黑色染料产品具有良好的耐洗牢度、高固着度和上染性、良好的上染性、清澈的残留染液等特性。
  • Reactive dye compound and preparation method and application thereof
    申请人:Zhejiang Keyong Chemical Co., Ltd.
    公开号:US11370921B2
    公开(公告)日:2022-06-28
    A reactive dye compound and preparation method and application for printing and dyeing of cellulosic fibers, polyamide fibers and fabrics thereof. Formula (I) is the dye compound structure where D1 and D2 are each independently the group of the following formula (a) or (b) or (c), and D1 and D2 are not simultaneously selected from the following formula (a). R1, R2, R4, R5, R7 and R8 are each independently H, linear or branched C1˜C4 alkyl, C1˜C4 alkoxy or sulfo; m=0-3. Each R3 is independently selected from amino, sulfo, ureido, C1˜C4 alkyl, C1˜C4 alkanoylamino or C1˜C4 alkoxy, n=0-3, and each R6 is independently selected from hydroxyl, amino and sulfo. X1, X2 and X3 are each independently H, C1˜C4 alkyl, C1˜C4 alkoxy, —SO2Y1, —NHCO(CH2)pSO2Y2 or —CONH(CH2)qSO2Y3, and at least one of D1 and D2 contains a fiber-reactive group. Y1˜Y3 are each independently —CH═CH2, —C2H4OSO3H or —CH2CH2Cl, p=1-3, and q=1-3.
    一种活性染料化合物及其制备方法和应用,用于纤维素纤维、聚酰胺纤维及其织物的印染。式(I)为染料化合物结构,其中 D1 和 D2 各自独立地为下式(a)或(b)或(c)的基团,且 D1 和 D2 不同时选自下式(a)。R1、R2、R4、R5、R7 和 R8 各自独立地为 H、直链或支链 C1˜C4烷基、C1˜C4 烷氧基或磺基;m=0-3。每个 R3 独立地选自基、磺基、基、C1˜C4 烷基、C1˜C4 烷酰基或 C1˜C4 烷氧基,n=0-3,每个 R6 独立地选自羟基、基和磺基。X1、X2 和 X3 各自独立地为 H、C1˜C4 烷基、C1˜C4 烷氧基、-SO2Y1、-NHCO(CH2)pSO2Y2 或 -CONH( )qSO2Y3,且 D1 和 D2 中至少有一个含有纤维反应基团。Y1˜Y3各自独立地为-CH═ 、-C2H4OSO3H或- Cl,p=1-3和q=1-3。
  • DETECTING TARGETS USING MASS TAGS AND MASS SPECTROMETRY
    申请人:Hong Rui
    公开号:US20130122516A1
    公开(公告)日:2013-05-16
    Particular disclosed embodiments disclosed herein concern using a one or more various mass tags, which can be specifically deposited at targets through direct or indirect enzymatic-catalyzed transformation, to provide a method for identifying targets in tissue samples. The mass tags may be labeled with stable isotopes to produce mass tags having the same chemical structure but different masses. Mass codes produced by ionizing the mass tags are detected and/or quantified using mass spectrometry. The method can be used for multiplexed detection of multiple targets in a particular sample. In some embodiments, a map divided into sections representing sections of the tissue sample may be prepared, with the map sections including data corresponding to quantification data wherein the size of a mass peak is determined and correlated with the amount of a target for the corresponding tissue sample section.
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫