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5,7-二氯-4-硝基苯并[c][1,2,5]噁二唑 | 15944-78-2

中文名称
5,7-二氯-4-硝基苯并[c][1,2,5]噁二唑
中文别名
——
英文名称
5,7-dichloro-4-nitro-2,1,3-benzoxadiazole
英文别名
4,6-dichloro-7-nitrobenzofurazan;4,6-Dichlor-7-nitro-benzofurazan;5,7-dichloro-4-nitro-benzo[1,2,5]oxadiazole
5,7-二氯-4-硝基苯并[c][1,2,5]噁二唑化学式
CAS
15944-78-2
化学式
C6HCl2N3O3
mdl
MFCD00460659
分子量
233.998
InChiKey
SCVFVTLATGCDGT-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):
    2.3
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    84.7
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    5,7-二氯-4-硝基苯并[c][1,2,5]噁二唑氢氧化钾 作用下, 生成 4,6-dihydroxy-7-nitrobenzofurazan
    参考文献:
    名称:
    Tsentovskii, V. M.; Evgen'ev, M. I.; Petukhova, L. V., Journal of general chemistry of the USSR, 1986, vol. 56, p. 1020 - 1023
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Agent and method for dyeing keratin fibers
    申请人:——
    公开号:US20030070239A1
    公开(公告)日:2003-04-17
    The present invention relates to a fiber-dyeing agent (A) prepared by mixing two components (A1) and (A2), said agent being characterized in that component (A1) contains at least one compound of formula (I) 1 wherein X denotes a halogen atom, a methoxy group or an ethoxy group; Y denotes an oxygen atom, a sulfur atom or a selenium atom; R1 and R2 are equal or different and independently of each other denote hydrogen, a halogen atom, a (C 1 -C 4 )-alkyl group, a halogen-substituted (C 1 -C 4 )-alkyl group, a (C 1 -C 4 )-alkoxy group, a nitro group, an acetamido group or an NR a R b group, wherein the R a and R b groups are equal or different and independently of each other denote hydrogen, a (C 1 -C 4 )-alkyl group, an optionally substituted aromatic carbon ring or a (C 1 -C 4 )-alkanecarbonyl group, or R a and R b together with the nitrogen atom form a heterocyclic (C 3 -C 6 ) group, and component (A2) contains at least one compound from the group consisting of amines, aminonitrobenzenes and phenols; to a method for dyeing hair by use of said agent, and to a multicomponent kit.
    本发明涉及一种纤维染料剂(A),其由混合两个组分(A1)和(A2)制备而成,其中该剂特征在于组分(A1)包含至少一个式(I)1的化合物,其中X表示卤素原子、甲基或乙基;Y表示原子、原子或原子;R1和R2相等或不同且独立地表示、卤素原子、(C1-C4)烷基、卤素取代的(C1-C4)烷基、(C1-C4)烷基、硝基、乙酰胺基或NRaRb基,其中Ra和Rb基相等或不同且独立地表示、(C1-C4)烷基、可选取代的芳环环或(C1-C4)烷基羰基基团,或Ra和Rb与原子一起形成杂环(C3-C6)基团,而组分(A2)包含至少一种来自胺、硝基苯的化合物组成的群体中的化合物;以及一种使用该剂染发的方法和多组分套装。
  • Method for producing optically active compound
    申请人:——
    公开号:US20020006645A1
    公开(公告)日:2002-01-17
    The present invention provides a method for industrially advantageously producing (S)-4-hydroxy-2-ketoglutaric acid and for producing compounds which are formed by biosynthesis from the precursor (S)-4-hydroxy-2-ketoglutaric acid, for example, for producing the compounds (2S,4S)-4-hydroxy-L-glutamic acid and (2S,4S)-4-hydroxy-L-proline, using a recombinant microorganism carrying a recombinant DNA harboring the DNA fragment encoding 4(S)-4-hydroxy-2-ketoglutaric acid aldolase gene.
    本发明提供了一种工业上优势生产(S)-4-羟基-2-戊二酸的方法,并利用携带重组DNA的重组生物生产由前体(S)-4-羟基-2-戊二酸生物合成的化合物,例如,用于生产化合物(2S,4S)-4-羟基-L-谷氨酸和(2S,4S)-4-羟基-L-脯氨酸,所述重组DNA携带编码4(S)-4-羟基-2-戊二酸醛缩酶基因的DNA片段。
  • Process for producing cis-3-hydroxy-L-proline
    申请人:KYOWA HAKKO KOGYO CO., LTD.
    公开号:EP0645457A2
    公开(公告)日:1995-03-29
    Provided is a process for industrially producing cis-3-hydroxy-L-proline useful as a raw material for medicines or as an additive to foods. L-proline is converted into cis-3-hydroxy-L-proline in the presence of an enzyme source which is derived from a microorganism belonging to the genus Streptomyces or Bacillus and which catalyzes hydroxylation of L-proline into cis-3-hydroxy-L-proline, a divalent iron ion and 2-ketoglutaric acid, in an aqueous medium, and the produced cis-3-hydroxy-L-proline is recovered from the aqueous medium. Also provided is a novel enzyme L-proline-3-hydroxylase, which is useful for the process.
    本发明提供了一种工业化生产可用作药物原料或食品添加剂顺式-3-羟基-L-脯氨酸的工艺。在一种酶源的存在下,L-脯氨酸被转化成顺式-3-羟基-L-脯氨酸,该酶源来自一种属于链霉菌属或芽孢杆菌属的微生物,它在介质中催化 L-脯氨酸羟化成顺式-3-羟基-L-脯氨酸、二价离子和 2-戊二酸,并从介质中回收生成的顺式-3-羟基-L-脯氨酸。此外,还提供了一种新型 L-脯氨酸-3-羟化酶,可用于该工艺。
  • ——
    作者:F. S. Levinson、S. I. Efimov、B. I. Buzykin、A. T. Gubaidullin、D. B. Krivolapov、I. A. Litvinov
    DOI:10.1023/a:1015017931597
    日期:——
    The molecular and crystal structures of 5,7-dichloro-4-nitro-2,1,3-benzoxadiazole and products of its reactions with hexamethyleneimine and dimethylamine were established by X-ray diffraction analysis. The molecular structures and the systems of hydrogen bonds in the crystals of these compounds are discussed.
  • L-proline-3-hydroxylase and process for producing cis-3-hydroxy-L-proline
    申请人:KYOWA HAKKO KOGYO CO., LTD.
    公开号:EP0645457B1
    公开(公告)日:1998-04-01
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重氮二硝基苯酚 达罗地平 苯并芙咱-5-硼酸频那醇酯 苯并氧化呋咱-5-羧酸 苯并呋扎-5-甲腈 苯并呋喃-5-磺酰氯 苯并呋喃-5-甲酸乙酯 苯并呋喃 苯并呋咱-5-羧酸乙酯 苯并呋咱-5-羧酸 苯并呋咱-5-碳酰氯 苯并呋咱 苯并二唑-4-甲醛 苯呋咱-5-三氟硼酸钾 硝基氨基吡咯烷苯并恶嗪 哌嗪酮,6-甲基-5-硫代-,(R)-(9CI) 去甲基伊拉地平 伊拉地平内酯 伊拉地平EP杂质A 伊拉地平 乙酮,1-[5-(丁基氨基)-2-羟基苯基]- NBD-双十六胺 N-[12-[((7-硝基-2-1,3-苯并恶二唑-4-基)氨基]十二烷酰基]-D-赤型-鞘氨醇 N-7-(4-硝基苯并-2-氧代-1,3-二氮唑)-omega-氨基己酸beta-(N-三甲基铵)乙酯 N-(7-硝基苯并-2-氧杂-1,3-二氮唑-4-基)磷脂酰乙醇胺 N-(3-氯-5-氟苯基)-4-硝基-2,1,3-苯并恶二唑-5-胺 N-(2-吗啉基乙基)-7-硝基-2,1,3-苯并恶二唑-4-胺 N,N-二甲基-7-硝基苯并呋咱-4-胺 N,N-二丁基-7-硝基-4-苯并呋咱胺 N'-[5-[[4-[5-(乙酰基-羟基氨基)戊基氨基]-4-氧代丁酰基]-羟基氨基]戊基]-N-羟基-N-[5-[(4-硝基-2,1,3-苯并恶二唑-7-基)氨基]戊基]丁二酰胺 EAM-1试剂 8-异米索前列醇 7-肼-N,N-二-4-苯并呋咱磺 7-硝基-N-[2-(2-吡啶基二硫代)乙基]-2,1,3-苯并恶二唑-4-胺 7-硝基-1-氧代-2,1,3-苯并恶二唑-1-鎓 7-甲氧基-2,1,3-苯并恶二唑-4-磺酰氯 7-氯苯并[c][1,2,5]噁二唑-4-胺 7-氯-N,N-二乙基-4-硝基-2,1,3-苯并恶二唑-5-胺 7-氯-4-硝基-5-哌啶基-2,1,3-苯并噁二唑 7-氯-4-硝基-2,1,3-苯并噁二唑1-氧化 7-氯-2,1,3-苯并噁二唑-4-磺酸 7-氟苯呋咱-4-磺酰胺 7-氟苯呋咱-4-硫氨 7-氟-2,1,3-苯并恶二唑-4-磺酰氯 7-哌啶-1-基-2,1,3-苯并恶二唑-4-胺 7-吗啉-4-基苯并[1,2,5]恶二唑-4-基胺 6-溴苯并[c][1,2,5]噁二唑1-氧化物 6-氟-2,1,3-苯并恶二唑-5-胺 6-[[7-(N,N-二甲氨基磺酰)-2,1,3-苯并恶二唑-4-基]氨基]己酸琥珀酰亚胺酯 6-[(7-硝基-2,1,3-苯并恶二唑-4-基)氨基]己酸