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2-氟-5-碘硝基苯 | 364-75-0

中文名称
2-氟-5-碘硝基苯
中文别名
——
英文名称
1-fluoro-4-iodo-2-nitrobenzene
英文别名
2-fluoro-5-iodonitrobenzene
2-氟-5-碘硝基苯化学式
CAS
364-75-0
化学式
C6H3FINO2
mdl
MFCD09800783
分子量
266.998
InChiKey
KUJTZQXHTBKAMO-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:
    289.4±20.0 °C(Predicted)
  • 密度:
    2.093±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    45.8
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2904909090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335
  • 储存条件:
    2-8℃

SDS

SDS:1ed63a65eb58e4dfa7e67416cf9da9e3
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 4-Iodo-2-nitrofluorobenzene
Synonyms: 1-Fluoro-4-iodo-2-nitrobenzene

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

Section 3. Composition/information on ingredients.
Ingredient name: 4-Iodo-2-nitrofluorobenzene
CAS number: 364-75-0

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: C6H3FINO2
Molecular weight: 267.0

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, hydrogen Iodide.

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-氟-5-碘硝基苯 在 potassium fluoride 、 氯化铵 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 反应 5.5h, 生成 N-(3-((2-amino-4-iodophenyl)amino)-5-(1H-pyrrol-1-yl)phenyl)acetamide
    参考文献:
    名称:
    PROTEIN KINASE INHIBITORS
    摘要:
    公式(I)的化合物中,其中R3、R4、G、B、M和Z如权利要求中所定义,并且其药学上可接受的盐已被披露。公式(I)的化合物具有作为FGFR抑制剂的效用,并且在需要FGFR激酶抑制的情况下,如癌症治疗中是有用的。
    公开号:
    US20150011548A1
  • 作为产物:
    描述:
    4-氟-3-硝基苯胺二碘甲烷亚硝酸异戊酯 作用下, 反应 2.0h, 以14%的产率得到2-氟-5-碘硝基苯
    参考文献:
    名称:
    [EN] PYRIDYL DERIVATIVES AND THEIR USE AS MGLU5 RECEPTOR ANTAGONISTS
    [FR] DERIVES DE PYRIDYLE ET LEUR UTILISATION EN TANT QU'ANTAGONISTES DU RECEPTEUR DE MGLU5
    摘要:
    本发明涉及公式(I)的吡啶衍生物作为mGlu5受体拮抗剂。因此,这些化合物可能对通过拮抗mGlu5受体而得到缓解的疾病的治疗或预防有用,其中Ar是苯基或萘基,每种基可能被一个或多个C1-C4烷基,C1-C4烷氧基,C1-C5酰基,卤素,氨基,硝基,氰基,羟基,C1-C5酰胺基,C1-C4烷基磺酰胺基,单-,二-或三氟代的C1-C3烷基,取代基可能相同也可能不同,并且可能带有CONH2,CONHCH3,CON(CH3)2,CO2H,CO2CH3,OCF3,CH2NHCOCH3,CH2NH2,CH2N(CH3)2,CH2CN,CH2OH,CH2NHSO2CH3,CH2N(CH3)(CH2)2CN,CH2N(CH3)CH(CH3)2,CH2NHCH(CH3)2,CH2NH(CH2)2CH3,CH2NHCO2R4,CH2NHCH2CH3,CH2NHCH3 NHCOC(CH3)2或N(S(O)2CH3)2取代基;R1是氢,卤素,R4,CN,C(NOH)R3,C(NO-R4)R3,(CH)2CO2R4,(CH2)nOR3,COR3,CF3,SR4,S(O)R4,S(O)2R4,COCH2CO2R3,NHSO2R4,NHCOR3,C(NOR3)NH2,CH2OCOR3,(CH2)nNH2,CON(CH3)2(CH2)nNHCO2R4,CO2R3,CONH2,CSNH2,C(NH)NHOR3,(CH2)nN(CH3)2或CONHNHCOR3;R2是1,2-乙烯二基或1,2-乙炔二基;R3是氢或C1-C4烷基;R4是C1-C4烷基;n为0,1,2,3或4;或其药学上可接受的盐,或其N-氧化物。
    公开号:
    WO2005094822A1
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文献信息

  • [EN] ALKYNYL ALCOHOLS AS KINASE INHIBITORS<br/>[FR] ALCOOLS D'ALCYNYLE UTILISÉS COMME INHIBITEURS DE KINASES
    申请人:AMGEN INC
    公开号:WO2009158011A1
    公开(公告)日:2009-12-30
    Selected compounds are effective for prophylaxis and treatment of inflammation and inflammatory disorders, such as NIK-mediated disorders. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, inflammation and the like.
    选定的化合物对预防和治疗炎症和炎症性疾病,如NIK介导的疾病,具有有效性。该发明涵盖了新颖的化合物、类似物、前药及其药用可接受的盐,以及用于预防和治疗涉及炎症等疾病和其他疾病或病症的药物组合物和方法。
  • [EN] INHIBITORS OF FIBROBLAST GROWTH FACTOR RECEPTOR KINASES<br/>[FR] INHIBITEURS DES KINASES RÉCEPTRICES DU FACTEUR DE CROISSANCE DES FIBROBLASTES
    申请人:KINNATE BIOPHARMA INC
    公开号:WO2021247969A1
    公开(公告)日:2021-12-09
    Provided herein are heteroaryl inhibitors of fibroblast growth factor receptor kinases, pharmaceutical compositions comprising said compounds, and methods for using said compounds for the treatment of diseases.
    提供了一种杂芳基的成纤维细胞生长因子受体激酶抑制剂,包括所述化合物的药物组合物,以及使用所述化合物治疗疾病的方法。
  • [EN] ACLY INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS D'ACLY ET LEURS UTILISATIONS
    申请人:NIMBUS ARTEMIS INC
    公开号:WO2020097408A1
    公开(公告)日:2020-05-14
    The present invention provides compounds useful as inhibitors of ATP citrate lyase (ACLY), compositions thereof, and methods of using the same.
    本发明提供了作为ATP柠檬酸裂合酶(ACLY)抑制剂的化合物、其组合物以及使用方法。
  • Unsymmetrical Aryl(2,4,6-trimethoxyphenyl)iodonium Salts: One-Pot Synthesis, Scope, Stability, and Synthetic Studies
    作者:Thomas L. Seidl、Sunil K. Sundalam、Brennen McCullough、David R. Stuart
    DOI:10.1021/acs.joc.5b02833
    日期:2016.3.4
    Diaryliodonium salts have recently attracted significant attention as metal-free-arylation reagents in organic synthesis, and efficient access to these salts is critical for advancement of their use in reaction discovery and development. The trimethoxybenzene-derived auxiliary is a promising component of unsymmetrical variants, yet access remains limited. Here, a one-pot synthesis of aryl(2,4,6-tr
    作为有机合成中的无金属芳构化试剂,二芳基碘鎓盐最近引起了广泛的关注,有效地获得这些盐对于促进其在反应发现和开发中的应用至关重要。三甲氧基苯衍生的助剂是不对称变体的有前途的组成部分,但访问仍然受到限制。在这里,一锅法合成的芳基(2,4,6-三甲氧基苯基)碘鎓盐是由芳基碘化物,m -CPBA,p描述了甲苯磺酸和三甲氧基苯。通过多变量分析的方法,可以优化用于一锅合成的反应条件。该反应快速(<1小时),提供高收率的产品(平均> 85%),并具有广泛的底物范围(> 25个实例),包括精制的芳基碘化物。这些试剂的实用性在与C-,N-,O-和S-亲核试剂的中等至高产率的芳基化反应中得到了证明,包括液晶分子的合成。
  • [EN] BENZIMIDAZOLE DERIVATIVES AND THEIR USE FOR MODULATING THE GABAA RECEPTOR COMPLEX<br/>[FR] DERIVES DE BENZIMIDAZOLE ET LEUR UTILISATION DANS LA MODULATION DU COMPLEXE RECEPTEUR GABAA
    申请人:NEUROSEARCH AS
    公开号:WO2004087137A1
    公开(公告)日:2004-10-14
    This invention relates to novel benzimidazole derivatives of formula (I), pharmaceutical compositions containing these compounds, and methods of treatment therewith. The compounds of the invention are useful in the treatment of central nervous system diseases and disorders, which are responsive to modulation of the GABAA receptor complex, and in particular for combating anxiety and related diseases.
    这项发明涉及公式(I)的新型苯并咪唑衍生物,含有这些化合物的药物组合物,以及使用这些化合物进行治疗的方法。该发明的化合物在治疗对GABAA受体复合物调节敏感的中枢神经系统疾病和紊乱方面具有用途,特别是用于对抗焦虑和相关疾病。
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