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4-溴-2-氟-5-甲基苯甲腈 | 916792-13-7

中文名称
4-溴-2-氟-5-甲基苯甲腈
中文别名
2-氟-4-溴-5-甲基苯腈
英文名称
4-bromo-2-fluoro-5-methylbenzonitrile
英文别名
——
4-溴-2-氟-5-甲基苯甲腈化学式
CAS
916792-13-7
化学式
C8H5BrFN
mdl
——
分子量
214.037
InChiKey
AVBKISZUVMWQIA-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:
    260.3±35.0℃ (760 Torr)
  • 密度:
    1.59±0.1 g/cm3 (20 ºC 760 Torr)
  • 闪点:
    111.2±25.9℃

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    23.8
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2926909090
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335
  • 储存条件:
    | 室温 |

SDS

SDS:8ae67b3f9480320746d13b7cf36d580f
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 4-Bromo-2-fluoro-5-methylbenzonitrile
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 4-Bromo-2-fluoro-5-methylbenzonitrile
CAS number: 916792-13-7

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.
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: C8H5BrFN
Molecular weight: 214.0

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 bromide.

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

  • 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:
    4-溴-2-氟-5-甲基苯甲腈N-溴代丁二酰亚胺(NBS)偶氮二异丁腈N-甲基吗啉氧化物 作用下, 以 四氢呋喃四氯化碳乙腈 为溶剂, 反应 28.0h, 生成 4-bromo-2-fluoro-5-[(3-fluorophenyl)hydroxymethyl]benzonitrile
    参考文献:
    名称:
    [EN] HETEROCYCLIC DERIVATIVES MODULATING ACTIVITY OF CERTAIN PROTEIN KINASES
    [FR] DÉRIVÉS HÉTÉROCYCLIQUES MODULANT L'ACTIVITÉ DE CERTAINES PROTÉINES KINASES
    摘要:
    本发明涉及具有通式(I)的新型杂环衍生物及其在癌症、炎症、疼痛、自身免疫疾病或阿尔茨海默病、帕金森病等神经退行性疾病的治疗中的应用,这些疾病可以通过调节特定蛋白激酶来治疗。通式(I)的化合物可用于治疗对目前可用药物组成的激酶抑制疗法无反应的患者。
    公开号:
    WO2016096709A1
  • 作为产物:
    描述:
    2-氟-5-甲基苯胺盐酸 、 tetra-N-butylammonium tribromide 、 sodium nitrite 作用下, 以 二氯甲烷 为溶剂, 反应 1.33h, 生成 4-溴-2-氟-5-甲基苯甲腈
    参考文献:
    名称:
    [EN] INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL
    [FR] INHIBITEURS DU CANAL POTASSIQUE MÉDULLAIRE EXTERNE RÉNAL
    摘要:
    本发明提供了式(I)的化合物及其药用盐,这些化合物是ROMK(Kir1.1)通道的抑制剂。这些化合物可用作利尿剂和/或钠利尿剂,并用于治疗和预防包括高血压、心力衰竭和慢性肾脏疾病在内的心血管疾病以及与过多盐分和水潴留有关的疾病。
    公开号:
    WO2016060941A1
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文献信息

  • [EN] COMPOUNDS<br/>[FR] COMPOSÉS
    申请人:CTXT PTY LTD
    公开号:WO2019243491A1
    公开(公告)日:2019-12-26
    A compound of formula (I), or a pharmaceutical salt thereof.
    式(I)的化合物,或其药用盐。
  • [EN] FUSED RING PYRIMIDONE DERIVATIVES FOR USE IN THE TREATMENT OF HBV INFECTION OR OF HBV-INDUCED DISEASES<br/>[FR] DÉRIVÉS DE PYRIMIDONE À CYCLES FUSIONNÉS DESTINÉS À ÊTRE UTILISÉS DANS LE TRAITEMENT D'UNE INFECTION PAR LE VIRUS DE L'HÉPATITE B OU DE MALADIES INDUITES PAR LE VIRUS DE L'HÉPATITE B
    申请人:JANSSEN SCIENCES IRELAND UNLIMITED CO
    公开号:WO2020182990A1
    公开(公告)日:2020-09-17
    The present application relates to compounds according to Formula (I), pharmaceutical compositions comprising at least one of said compounds, their use as a medicament, and their use in treating chronic hepatitis B virus (HBV) infection. The disclosure further pertains to methods for preparing compounds according to Formula (I).
    本申请涉及按照式(I)的化合物,包括至少一种所述化合物的药物组合物,其作为药物的用途,以及其在治疗慢性乙型肝炎病毒(HBV)感染中的用途。该公开还涉及按照式(I)制备化合物的方法。
  • [EN] ANNELATED PYRROLES AND THEIR USE AS CRAC INHIBITORS<br/>[FR] PYRROLES CONDENSÉS ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE CRAC
    申请人:GRUENENTHAL GMBH
    公开号:WO2015022073A1
    公开(公告)日:2015-02-19
    The invention relates to substituted bicyclic pyrroloheterocyclyl compounds of general formula (I), wherein A1 and A2 represent direct bond or C(=O), with the proviso that 0 or 1 of A1 and A2 represents C(=O); m and n independently denote 0, 1, 2 or 3, with the proviso that the sum [n + m] is 1, 2, 3 or 4; R1 denotes H, F, CI, Br, I, CN, CF3, CF2H, CFH2, CO2H, CO2R13, R13, OH. O-R13, NH2, N(H)R13, N(R13)2, R2 represents 0 to 4 substituents, each independently selected from F, CI, Br, CN. CF3, CF2H, CFH2, R13, OH, O-R13, NH2, N(H)R13 and N(R13)2; Ar1 represents phenyl or 5- or 6-membered heteroaryl, in each case unsubstituted or substituted with one, two, three or four substituents, independently selected from F, CI, Br, CN, CF3. CF2H, CFH2, R13 and O- R13; or C3-6-cycloalkyl or 3 to 7 membered heterocycloalkyl, in each case unsubstituted or mono- or polysubstituted; Ar2 represents phenyl or 5- or 6-membered heteroaryl, wherein said phenyl or said heteroaryl may be unsubstituted or mono- or polysubstituted and may be condensed with a 4-, 5-, 6-or 7- membered ring, being carbocyclic or heterocyclic, wherein said condensed ring may be saturated, partially unsaturated or aromatic and may be unsubstituted or mono- or polysubstituted; useful as ICRAC inhibitors, to pharmaceutical compositions containing these compounds and to these compounds for the use in the treatment and/or prophylaxis of diseases and/or disorders, in particular inflammatory diseases and/or inflammatory disorders.
    该发明涉及通式(I)的取代双环吡咯杂环基化合物,其中A1和A2代表直接键或C(=O),但A1和A2中的0或1个代表C(=O);m和n独立地表示0、1、2或3,但要求总和[n + m]为1、2、3或4;R1代表H、F、CI、Br、I、CN、CF3、CF2H、CFH2、CO2H、CO2R13、R13、OH、O-R13、NH2、N(H)R13、N(R13)2;R2表示0到4个取代基,每个独立地选自F、CI、Br、CN、CF3、CF2H、CFH2、R13、OH、O-R13、NH2、N(H)R13和N(R13)2;Ar1表示苯基或5-或6-成员杂芳基,每种情况下未取代或取代为一个、两个、三个或四个取代基,独立地选自F、CI、Br、CN、CF3、CF2H、CFH2、R13和O-R13;或C3-6-环烷基或3到7-成员杂环烷基,每种情况下未取代或单取代或多取代;Ar2表示苯基或5-或6-成员杂芳基,其中所述苯基或所述杂芳基可以未取代或单取代或多取代,并且可以与4-、5-、6-或7-成员环融合,为碳环或杂环,所述融合环可以饱和、部分不饱和或芳香,并且可以未取代或单取代或多取代;用作ICRAC抑制剂,用于含有这些化合物的药物组合物,以及用于治疗和/或预防疾病和/或疾病,特别是炎症性疾病和/或炎症性疾病的这些化合物。
  • [EN] 6-(5-HYDROXY-1H-PYRAZOL-1-YL)NICOTINAMIDE DERIVATIVES AND THEIR USE AS PHD INHIBITORS<br/>[FR] INHIBITEURS 6-(5-HYDROXY-1H-PYRAZOL-1-YL)NICOTINAMIDE DE PHD
    申请人:TAKEDA PHARMACEUTICAL
    公开号:WO2014160810A1
    公开(公告)日:2014-10-02
    The present invention provides compounds of formula (I) which are useful as inhibitors of PHD, pharmaceutical compositions thereof, methods for treatment of conditions associated with HIF, processes for making the compounds and intermediates thereof.
    本发明提供了公式(I)的化合物,这些化合物可用作PHD的抑制剂,以及与HIF相关疾病的治疗方法,制备这些化合物及其中间体的药物组合物。
  • [EN] FUSED BICYCLIC HETEROARYL DERIVATIVES HAVING ACTIVITY AS PHD INHIBITORS<br/>[FR] DÉRIVÉS HÉTÉROARYLES BICYCLIQUES FUSIONNÉS AYANT UNE ACTIVITÉ D'INHIBITEURS DE PHD
    申请人:TAKEDA PHARMACEUTICALS CO
    公开号:WO2016148306A1
    公开(公告)日:2016-09-22
    The present invention provides compounds of formula (I) and pharmaceutically acceptable salts thereof, formula (I) wherein X1 , X2, X 3, Y1 , Y 2, R 1, R2 and R3 are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.
    本发明提供了式(I)的化合物及其药用盐,式(I)中X1,X2,X3,Y1,Y2,R1,R2和R3如规范中所定义,其制备方法,含有它们的药物组合物以及它们在治疗中的用途。
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