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5-溴-3-氯-2-氟苯甲醛 | 1280786-80-2

中文名称
5-溴-3-氯-2-氟苯甲醛
中文别名
——
英文名称
5-bromo-3-chloro-2-fluorobenzaldehyde
英文别名
——
5-溴-3-氯-2-氟苯甲醛化学式
CAS
1280786-80-2
化学式
C7H3BrClFO
mdl
——
分子量
237.456
InChiKey
PLYXMAYYYOIEJW-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:
    263.5±35.0 °C(Predicted)
  • 密度:
    1.779±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2913000090
  • 危险性防范说明:
    P280,P305+P351+P338
  • 危险性描述:
    H317,H319
  • 储存条件:
    存于室温下,请密封并保持干燥。

SDS

SDS:513f15162b4ac87861ad1b6712ec0289
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 5-Bromo-3-chloro-2-fluorobenzaldehyde
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 5-Bromo-3-chloro-2-fluorobenzaldehyde
CAS number: 1280786-80-2

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: C7H3BrClFO
Molecular weight: 237.5

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, hydrogen chloride, 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:
    5-溴-3-氯-2-氟苯甲醛甲醇 、 sodium tetrahydroborate 作用下, 反应 2.0h, 以96.6%的产率得到(5-溴-3-氯-2-氟苯基)甲醇
    参考文献:
    名称:
    [EN] THERAPEUTIC INHIBITORY COMPOUNDS
    [FR] COMPOSÉS INHIBITEURS THÉRAPEUTIQUES
    摘要:
    公开号:
    WO2017098328A8
  • 作为产物:
    描述:
    3-氯-4-氟溴苯N,N-二甲基甲酰胺正丁基锂二异丙胺 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 0.75h, 以76%的产率得到5-溴-3-氯-2-氟苯甲醛
    参考文献:
    名称:
    [EN] PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII
    [FR] MACROCYCLES PEPTIDIQUES CONTRE ACINETOBACTER BAUMANNII
    摘要:
    本发明提供了式(I)的化合物,其中X1至X8和R1至R8如本文所述,以及其药学上可接受的盐。此外,本发明涉及制备式(I)的化合物,包括它们的药物组合物以及它们作为治疗由鲍曼不动杆菌引起的疾病和感染的药物的用途。
    公开号:
    WO2017072062A1
点击查看最新优质反应信息

文献信息

  • [EN] PYRIMIDINE DERIVATIVES AS PGE2 RECEPTOR MODULATORS<br/>[FR] DÉRIVÉS DE PYRIMIDINE UTILISÉS EN TANT QUE MODULATEURS DES RÉCEPTEURS DES PGE2
    申请人:IDORSIA PHARMACEUTICALS LTD
    公开号:WO2018210988A1
    公开(公告)日:2018-11-22
    The present invention relates to pyrimidine derivatives of formula (I) wherein (R1)n, R3, R4a, R4b, R5a, R5b and Ar1 are as described in the description and their use in the treatment of cancer by modulating an immune response comprising a reactivation of the immune system in the tumor. The invention further relates to novel benzofurane and benzothiophene derivatives of formula (II) and their use as pharmaceuticals, to their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as modulators of the prostaglandin 2 receptors EP2 and/or EP4.
    本发明涉及式(I)的嘧啶衍生物,其中(R1)n,R3,R4a,R4b,R5a,R5b和Ar1如描述中所述,以及它们通过调节免疫反应,包括肿瘤中免疫系统的再激活,用于治疗癌症。本发明进一步涉及新颖的苯并呋喃和苯并噻吩衍生物式(II),及其作为药物的使用,其制备,药用可接受的盐,及其作为药物的使用,以及包含式(I)中一个或多个化合物的药物组合物,尤其是它们作为前列腺素2受体EP2和/或EP4的调节剂的使用。
  • HETEROCYCLIC COMPOUND, APPLICATION THEREOF AND PHARMACEUTICAL COMPOSITION COMPRISING SAME
    申请人:SUZHOU SINOVENT PHARMACEUTICALS CO., LTD.
    公开号:US20200369676A1
    公开(公告)日:2020-11-26
    Disclosed in the present invention are a heterocyclic compound, an application thereof and a pharmaceutical composition comprising the same. Provided by the present invention are a heterocyclic compound represented by formula I or a pharmaceutically acceptable salt thereof. The compound has a novel structure and a good inhibitory activity against autotaxin (ATX).
    本发明涉及一种杂环化合物及其应用和包含该化合物的药物组合物。本发明提供了一种由式I表示的杂环化合物或其药用可接受盐。该化合物具有新颖的结构,并且对自动税脂酶(ATX)具有良好的抑制活性。
  • [EN] CYCLIC COMPOUNDS AND USES THEREOF<br/>[FR] COMPOSÉS CYCLIQUES ET LEURS UTILISATIONS
    申请人:KARYOPHARM THERAPEUTICS INC
    公开号:WO2016100515A1
    公开(公告)日:2016-06-23
    The invention generally relates to substituted benzothiophenyl, substituted benzothiazolyl, substituted indolyl and substituted benzoimidazolyl compounds and, more particularly, to a compound represented by Structural Formula I: or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of Structural Formula I, or a pharmaceutically acceptable salt or composition thereof, e.g., in the treatment of a disease or disorder selected from cancer (e.g., lymphoma, such as mantle cell lymphoma), a neurodegenerative disease, inflammatory diseases or an autoimmune system disease (e.g., a T-Cell mediated autoimmune disesase).
    该发明通常涉及取代苯并噻吩基、取代苯并噻唑基、取代吲哚基和取代苯并咪唑基化合物,更具体地,涉及一种由结构式I表示的化合物或其药学上可接受的盐,其中变量如本文所定义和描述。该发明还包括合成和使用结构式I的化合物,或其药学上可接受的盐或组合物,例如,在治疗癌症(例如淋巴瘤,如袍细胞淋巴瘤)、神经退行性疾病、炎症性疾病或自身免疫系统疾病(例如T细胞介导的自身免疫疾病)中的应用。
  • [EN] CYCLOPROPYLDERIVATIVES AND THEIR USE AS KINASE INHIBITORS<br/>[FR] DÉRIVÉS DE CYCLOPROPYLE ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE KINASE
    申请人:KARYOPHARM THERAPEUTICS INC
    公开号:WO2017031204A1
    公开(公告)日:2017-02-23
    The invention generally relates to cyclic compounds and, more particularly, to a compound represented by Structural Formula I: or a pharmaceutically acceptable salt thereof and pharmaceutical comopositions comprising the multicyclic compounds. The invention also relates to a method for treating a disease or disorder selected from cancer (e.g., lymphoma, such as mantle cell lymphoma), a neurodegenerative disease, an inflammatory diseases or an immune system disease (e.g., a T-Cell mediated autoimmune disesase) in a subject in need thereof. The method comprises administering to a subject in need thereof a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, or a composition comprising a compound of the invention, or a pharmaceutically acceptable salt thereof.
    该发明通常涉及环状化合物,更具体地涉及由结构式I表示的化合物:或其药学上可接受的盐以及包含多环化合物的药物组合物。该发明还涉及一种治疗癌症(例如,淋巴瘤,如袍细胞淋巴瘤)、神经退行性疾病、炎症性疾病或免疫系统疾病(例如,T细胞介导的自身免疫疾病)的方法,该方法用于治疗需要的受试者。该方法包括向需要的受试者施用该发明的化合物或其药学上可接受的盐的治疗有效量,或者包含该发明的化合物或其药学上可接受的盐的组合物。
  • [EN] MULTICYCLIC COMPOUNDS AND USES THEREOF<br/>[FR] COMPOSÉS MULTICYCLIQUES ET LEURS UTILISATIONS
    申请人:KARYOPHARM THERAPEUTICS INC
    公开号:WO2017117447A1
    公开(公告)日:2017-07-06
    The present invention relates to multicyclic compounds containing a urea or a guanidine moiety, or pharmaceutically acceptable salts or compositions thereof represented by Structural Formula (IA) or a pharmaceutically acceptable salt thereof and pharmaceutical comopositions comprising the multicyclic compounds. The invention also relates to a method for treating a disease or disorder selected from cancer (e.g., lymphoma, such as mantle cell lymphoma), a neurodegenerative disease, an inflammatory diseases or an immune system disease (e.g., a T-Cell mediated autoimmune disesase) in a subject in need thereof. The method comprises administering to a subject in need thereof a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, or a composition comprising a compound of the invention, or a pharmaceutically acceptable salt thereof.
    本发明涉及含有脲基或胍基部分的多环化合物,或其结构式(IA)所代表的药学上可接受的盐或组合物,或其药学上可接受的盐,以及包含这些多环化合物的药物组合物。该发明还涉及一种治疗癌症(如淋巴瘤,如袖珍细胞淋巴瘤)、神经退行性疾病、炎症性疾病或免疫系统疾病(如T细胞介导的自身免疫疾病)的方法,该方法包括向需要的受试者施用本发明化合物的治疗有效量,或其药学上可接受的盐,或包含本发明化合物的组合物,或其药学上可接受的盐。
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