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2-(2-氟苯氧基)乙酰肼 | 380426-61-9

中文名称
2-(2-氟苯氧基)乙酰肼
中文别名
2-(2-氟苯氧基)乙烷肼
英文名称
2-fluorophenoxyacetic acid hydrazide
英文别名
2-(2-fluorophenoxy)acetohydrazide
2-(2-氟苯氧基)乙酰肼化学式
CAS
380426-61-9
化学式
C8H9FN2O2
mdl
MFCD02295759
分子量
184.17
InChiKey
XTXWVVVBLMYXNP-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):
    0.4
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.125
  • 拓扑面积:
    64.4
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2928000090

SDS

SDS:e34d0db2736269f486a8a6497d9acb98
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2-(2-Fluorophenoxy)acetohydrazide
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

Section 3. Composition/information on ingredients.
Ingredient name: 2-(2-Fluorophenoxy)acetohydrazide
CAS number: 380426-61-9

Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels, refrigerated.
Storage:

Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

Section 9. Physical and chemical properties
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C8H9FN2O2
Molecular weight: 184.2

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides, hydrogen fluoride.

Section 11. Toxicological information
No data.

Section 12. Ecological information
No data.

Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

Section 14. Transportation information
Non-harzardous for air and ground transportation.

Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.


SECTION 16 - ADDITIONAL INFORMATION
N/A

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:
    2-(2-氟苯氧基)乙酰肼吡啶2,6-二甲基吡啶三氟甲磺酸酐 作用下, 以 二氯甲烷 为溶剂, 反应 15.5h, 生成 3-[5-(2-fluorophenoxy)methyl-1,3,4-oxadiazol-2-yl]-2H-chromen-2-one
    参考文献:
    名称:
    新香豆素附加恶二唑的合成、结构分析、DFT 计算和能量框架,通过靶向 VEGF 介导的血管生成来逆转腹水恶性肿瘤
    摘要:
    腹水恶性肿瘤是发病率的常见原因,并且在许多癌症中存在严重的管理问题。血管生成通过血管内皮生长因子 (VEGF) 在腹水肿瘤的预后中起主要作用。抑制VEGF是腹水肿瘤消退的关键策略之一。该研究的目的是合成一类新型 VEGF 抑制剂,用于治疗腹水肿瘤恶性肿瘤。作为一种方法,在多步骤过程中合成了一系列新的 1, 3, 4-恶二唑衍生物,其中包含香豆素-3-取代的芳基和杂芳基部分 ( 7a-l )。这些化合物的结构通过 IR、1 H、13C、核磁共振、质谱和元素分析。新合成的分子通过 MTT 和台盼蓝试验针对 ACHN、A375、SIHA、Skov3 和 EAC 等多种细胞系进行细胞筛选,鉴定出IC 50 -9 µM 的化合物 ( 7k )为铅生物活性分子。此外,VEGF 诱导的非致瘤性 CAM 和 RAT 角膜试验揭示了化合物 ( 7k ) 的血管预防功效。在体外研究中证明了VEGF的表达和相对
    DOI:
    10.1016/j.molstruc.2021.132173
  • 作为产物:
    描述:
    2-氟苯酚potassium carbonate一水合肼 作用下, 以 乙醇丙酮 为溶剂, 生成 2-(2-氟苯氧基)乙酰肼
    参考文献:
    名称:
    新香豆素附加恶二唑的合成、结构分析、DFT 计算和能量框架,通过靶向 VEGF 介导的血管生成来逆转腹水恶性肿瘤
    摘要:
    腹水恶性肿瘤是发病率的常见原因,并且在许多癌症中存在严重的管理问题。血管生成通过血管内皮生长因子 (VEGF) 在腹水肿瘤的预后中起主要作用。抑制VEGF是腹水肿瘤消退的关键策略之一。该研究的目的是合成一类新型 VEGF 抑制剂,用于治疗腹水肿瘤恶性肿瘤。作为一种方法,在多步骤过程中合成了一系列新的 1, 3, 4-恶二唑衍生物,其中包含香豆素-3-取代的芳基和杂芳基部分 ( 7a-l )。这些化合物的结构通过 IR、1 H、13C、核磁共振、质谱和元素分析。新合成的分子通过 MTT 和台盼蓝试验针对 ACHN、A375、SIHA、Skov3 和 EAC 等多种细胞系进行细胞筛选,鉴定出IC 50 -9 µM 的化合物 ( 7k )为铅生物活性分子。此外,VEGF 诱导的非致瘤性 CAM 和 RAT 角膜试验揭示了化合物 ( 7k ) 的血管预防功效。在体外研究中证明了VEGF的表达和相对
    DOI:
    10.1016/j.molstruc.2021.132173
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文献信息

  • [EN] BENZODIAZEPINE DERIVATIVES, COMPOSITIONS, AND METHODS FOR TREATING COGNITIVE IMPAIRMENT<br/>[FR] DÉRIVÉS DE BENZODIAZÉPINE, COMPOSITIONS ET MÉTHODES DE TRAITEMENT DE LA DÉFICIENCE COGNITIVE
    申请人:MEKONNEN BELEW
    公开号:WO2016205739A1
    公开(公告)日:2016-12-22
    This invention relates to benzodiazepine derivatives, compositions comprising therapeutically effective amounts of those benzodiazepine derivatives and methods of using those derivatives or compositions in treating cognitive impairment associated with central nervous system (CNS) disorders. In particular, it relates to the use of a α5- containing GABAA receptor agonist (e.g., a α5-containing GABAA receptor positive allosteric modulator) as described herein in treating cognitive impairment associated with central nervous system (CNS) disorders in a subject in need or at risk thereof, including, without limitation, subjects having or at risk for age-related cognitive impairment, Mild Cognitive Impairment (MCI), amnestic MCI (aMCI), Age- Associated Memory Impairment (AAMI), Age Related Cognitive Decline (ARCD), dementia, Alzheimer' s Disease(AD), prodromal AD, post traumatic stress disorder (PTSD), schizophrenia, bipolar disorder, amyotrophic lateral sclerosis (ALS), cancer-therapy-related cognitive impairment, mental retardation, Parkinson' s disease (PD), autism spectrum disorders, fragile X disorder, Rett syndrome, compulsive behavior, and substance addiction.
    这项发明涉及苯二氮卓啉衍生物,包括含有这些苯二氮卓啉衍生物的治疗有效量的组合物,以及使用这些衍生物或组合物治疗与中枢神经系统(CNS)疾病相关的认知障碍的方法。具体而言,它涉及在需要或有风险的受试者中治疗与中枢神经系统(CNS)疾病相关的认知障碍,包括但不限于具有或有风险患上与年龄相关的认知障碍、轻度认知障碍(MCI)、遗忘性MCI(aMCI)、年龄相关记忆障碍(AAMI)、年龄相关认知衰退(ARCD)、痴呆症、阿尔茨海默病(AD)、前驱期AD、创伤后应激障碍(PTSD)、精神分裂症、躁郁症、肌萎缩侧索硬化(ALS)、癌症治疗相关认知障碍、智力障碍、帕金森病(PD)、自闭症谱系障碍、脆性X综合症、雷特综合症、强迫行为和物质成瘾。
  • BENZODIAZEPINE DERIVATIVES, COMPOSITIONS, AND METHODS FOR TREATING COGNITIVE IMPAIRMENT
    申请人:AgeneBio, Inc.
    公开号:US20180170941A1
    公开(公告)日:2018-06-21
    This invention relates to benzodiazepine derivatives, compositions comprising therapeutically effective amounts of those benzodiazepine derivatives and methods of using those derivatives or compositions in treating cognitive impairment associated with central nervous system (CNS) disorders. In particular, it relates to the use of a α5-containing GABA A receptor agonist (e.g., a α5-containing GABA A receptor positive allosteric modulator) as described herein in treating cognitive impairment associated with central nervous system (CNS) disorders in a subject in need or at risk thereof, including, without limitation, subjects having or at risk for age-related cognitive impairment, Mild Cognitive Impairment (MCI), amnestic MCI (aMCI), Age-Associated Memory Impairment (AAMI), Age Related Cognitive Decline (ARCD), dementia, Alzheimer's Disease(AD), prodromal AD, post traumatic stress disorder (PTSD), schizophrenia, bipolar disorder, amyotrophic lateral sclerosis (ALS), cancer-therapy-related cognitive impairment, mental retardation, Parkinson's disease (PD), autism spectrum disorders, fragile X disorder, Rett syndrome, compulsive behavior, and substance addiction. It also relates to the use of a α5-containing GABA A receptor agonist (e.g., a α5-containing GABA A receptor positive allosteric modulator) as described herein in treating brain cancers (including brain tumors, e.g., medulloblastomas), and cognitive impairment associated therewith.
    这项发明涉及苯二氮卓啉衍生物,包括含有这些苯二氮卓啉衍生物的治疗有效量的组合物,以及使用这些衍生物或组合物治疗与中枢神经系统(CNS)疾病相关的认知障碍的方法。具体而言,它涉及在需要或有风险的受试者中治疗与中枢神经系统(CNS)疾病相关的认知障碍,包括但不限于患有或有风险患有与年龄相关的认知障碍、轻度认知障碍(MCI)、遗忘性MCI(aMCI)、年龄相关记忆障碍(AAMI)、年龄相关认知衰退(ARCD)、痴呆症、阿尔茨海默病(AD)、前驱期AD、创伤后应激障碍(PTSD)、精神分裂症、躁郁症、肌萎缩侧索硬化(ALS)、癌症治疗相关认知障碍、智力障碍、帕金森病(PD)、自闭症谱系障碍、脆性X综合症、瑞特综合症、强迫行为和物质成瘾。它还涉及在治疗与之相关的脑癌(包括脑肿瘤,例如髓母细胞瘤)和认知障碍的情况下,如本文所述使用α5含有的GABAA受体激动剂(例如,α5含有的GABAA受体正向变构调节剂)。
  • Synthesis and xanthine oxidase inhibitory activity of 7-methyl-2-(phenoxymethyl)-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-one derivatives
    作者:K.R. Sathisha、Shaukath A. Khanum、J.N. Narendra Sharath Chandra、F. Ayisha、S. Balaji、Gopal K. Marathe、Shubha Gopal、K.S. Rangappa
    DOI:10.1016/j.bmc.2010.11.034
    日期:2011.1
    gastrointestinal upset, skin rashes and hypersensitivity reactions. Moreover, an elevated level of uric acid is considered as an independent risk factor for cardiovascular diseases. Therefore use of allopurinol-like drugs with minimum side effects is the ideal drug of choice against gout. In this study, we report the synthesis of a series of pyrimidin-5-one analogues as effective and a new class of xanthine oxidase
    血尿酸水平升高(高尿酸血症)是痛风的根本原因。黄嘌呤氧化酶是催化次黄嘌呤氧化为黄嘌呤然后变为尿酸的关键酶。别嘌醇是一种广泛使用的黄嘌呤氧化酶抑制剂,是治疗痛风的最常用药物。但是,一小部分人却遭受别嘌醇的不良影响,包括胃肠道不适,皮疹和超敏反应。此外,尿酸水平升高被认为是心血管疾病的独立危险因素。因此,使用副作用最小的类别嘌呤醇类药物是对抗痛风的理想药物选择。在这项研究中,我们报告了一系列有效的嘧啶5一类似物和一类新的黄嘌呤氧化酶抑制剂的合成。所有合成的嘧啶-5-酮类似物均通过光谱技术和元素分析进行​​表征。四(在该类别的20个合成分子中,图6a,6b,6d和6f)显示出对三种不同的黄嘌呤氧化酶的良好抑制作用,基于它们各自的IC 50值,它们比别嘌呤醇更有效。分子建模和对接研究表明,分子6a与黄嘌呤氧化酶的关键成分钼-氧-硫(MOS)复合物具有很好的相互作用。这些结果突出了鉴定出一种新型的黄
  • 2,5-取代基-1,3,4-噁(噻)二唑硫醚类衍生物、其制备方法及应用
    申请人:贵州大学
    公开号:CN106432125A
    公开(公告)日:2017-02-22
    本发明公开了一种2,5‑取代基‑1,3,4‑噁(噻)二唑硫醚类衍生物、其制备方法及应用,其通式如下:(I)其中:R1为4‑氯苯基、4‑氟苯基、4‑甲基苯基、4‑甲氧基苯基、4‑硝基苯基、4‑氰基‑3,5‑二氟苯基、4‑三氟甲基苯基、4‑三氟甲氧基苯基、4‑叔丁基苯基、2‑氟苯基等取代基;R2为甲基、乙基、4‑氯苄基、2,4‑二氯苄基、4‑三氟甲氧基、苄基、4‑氟苄基、4‑氯苄基等取代基;X为O或S。本发明的化合物可用作杀农作物线虫和抑制作物细菌性病的药物。
  • [EN] BENZODIAZEPINE DERIVATIVES, COMPOSITIONS, AND METHODS FOR TREATING COGNITIVE IMPAIRMENT<br/>[FR] DÉRIVÉS DE BENZODIAZÉPINE, COMPOSITIONS ET PROCÉDÉS DE TRAITEMENT DE LA DÉFICIENCE COGNITIVE
    申请人:AGENEBIO INC
    公开号:WO2015095783A1
    公开(公告)日:2015-06-25
    This invention relates to benzodiazepine derivatives, compositions comprising therapeutically effective amounts of those benzodiazepine derivatives and methods of using those derivatives or compositions in treating cognitive impairment associated with central nervous system (CNS) disorders. In particular, it relates to the use of a a5- containing GABAA receptor agonist (e.g., a α5 -containing GABAA receptor positive allosteric modulator) as described herein in treating cognitive impairment associated with central nervous system (CNS) disorders in a subject in need or at risk thereof, including, without limitation, subjects having or at risk for age-related cognitive impairment, Mild Cognitive Impairment (MCI), amnestic MCI (aMCI), Age-Associated Memory Impairment (AAMI), Age Related Cognitive Decline (ARCD), dementia, Alzheimer's Disease(AD), prodromal AD, post traumatic stress disorder (PTSD), schizophrenia, bipolar disorder, amyotrophic lateral sclerosis (ALS), cancer-therapy-related cognitive impairment, mental retardation, Parkinson's disease (PD), autism spectrum disorders, fragile X disorder, Rett syndrome, compulsive behavior, and substance addiction.
    这项发明涉及苯二氮卓啉衍生物,包括含有这些苯二氮卓啉衍生物的治疗有效量的组合物,以及使用这些衍生物或组合物治疗与中枢神经系统(CNS)疾病相关的认知障碍的方法。具体而言,它涉及在需要或有风险的受试者中治疗与中枢神经系统(CNS)疾病相关的认知障碍,包括但不限于患有或有风险患有与年龄相关的认知障碍、轻度认知障碍(MCI)、遗忘性MCI(aMCI)、年龄相关记忆障碍(AAMI)、年龄相关认知衰退(ARCD)、痴呆、阿尔茨海默病(AD)、前驱期AD、创伤后应激障碍(PTSD)、精神分裂症、躁郁症、肌萎缩侧索硬化(ALS)、癌症治疗相关认知障碍、智力障碍、帕金森病(PD)、自闭症谱系障碍、脆性X综合症、瑞特综合症、强迫行为和物质成瘾中所述的α5-含GABAA受体激动剂(例如,α5-含GABAA受体正向变构调节剂)的使用。
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