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3-溴-2-氯-4-甲基吡啶 | 55404-31-4

中文名称
3-溴-2-氯-4-甲基吡啶
中文别名
2-氯-3-溴-4-甲基吡啶
英文名称
3-bromo-2-chloro-4-methylpyridine
英文别名
3-bromo-2-chloro-4-picoline
3-溴-2-氯-4-甲基吡啶化学式
CAS
55404-31-4
化学式
C6H5BrClN
mdl
MFCD04112511
分子量
206.469
InChiKey
QPFHYDFGKXHWIN-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:
    250.3±35.0 °C(Predicted)
  • 密度:
    1.624±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.166
  • 拓扑面积:
    12.9
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2933399090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

SDS

SDS:4374bdb04ae1d26e7e6007971cbe30a6
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 3-Bromo-2-chloro-4-picoline
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 3-Bromo-2-chloro-4-picoline
CAS number: 55404-31-4

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: C6H5BrClN
Molecular weight: 206.5

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 chloride, 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

  • 上游原料
    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:
    3-溴-2-氯-4-甲基吡啶 在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 反应 1.08h, 生成 2-(4-甲氧基苄氧基)-3-溴-4-甲基吡啶
    参考文献:
    名称:
    WO2008/11109
    摘要:
    公开号:
  • 作为产物:
    描述:
    3-溴-4-甲基吡啶N-氧化物三氯氧磷 作用下, 以38%的产率得到3-溴-2-氯-4-甲基吡啶
    参考文献:
    名称:
    [EN] MACROCYCLIC DERIVATIVES FOR THE TREATMENT OF PROLIFERATIVE DISEASES
    [FR] DÉRIVÉS MACROCYCLIQUES POUR LE TRAITEMENT DE MALADIES PROLIFÉRATIVES
    摘要:
    该发明涉及本文进一步定义的Φ式化合物及其药用盐,包括含有这些化合物和盐的药物组合物,以及它们的用途。本发明的化合物和盐抑制间变性淋巴瘤激酶(ALK)和/或EML4-ALK,并且适用于治疗或改善异常细胞增殖性疾病,如癌症。
    公开号:
    WO2013132376A1
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文献信息

  • Aryl nitrogen-containing bicyclic compounds and methods of use
    申请人:Patel F. Vinod
    公开号:US20070054916A1
    公开(公告)日:2007-03-08
    The present invention comprises a new class of compounds useful for the prophylaxis and treatment of protein kinase mediated diseases, including inflammation, cancer and related conditions. The compounds have a general Formula I wherein A 1 , A 2 , A 3 , B, R 1 , R 2 , R 3 and R 4 are defined herein. Accordingly, the invention also comprises pharmaceutical compositions comprising the compounds of the invention, methods for the prophylaxis and treatment of kinase mediated diseases using the compounds and compositions of the invention, and intermediates and processes useful for the preparation of compounds of the invention.
    这项发明涉及一类新的化合物,用于预防和治疗蛋白激酶介导的疾病,包括炎症、癌症和相关疾病。这些化合物具有一般的化学式I,其中A1、A2、A3、B、R1、R2、R3和R4在此有定义。因此,该发明还涉及包括该发明的化合物的药物组合物,使用该发明的化合物和组合物预防和治疗激酶介导的疾病的方法,以及用于制备该发明的化合物的中间体和方法。
  • KINASE INHIBITORS
    申请人:Allergan, Inc.
    公开号:US20160096832A1
    公开(公告)日:2016-04-07
    The present invention relates to organic molecules capable of modulating tyrosine kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation.
    本发明涉及有机分子,能够调节酪氨酸激酶信号传导,以调节、调控和/或抑制异常细胞增殖。
  • [EN] FLUORINATED QUINOLINE AND QUINOXALINE DERIVATIVES AS DIHYDROOROTATE DEHYDROGENASE (DHODH) INHIBITORS FOR THE TREATMENT OF CANCER, AUTOIMMUNE AND INFLAMMATORY DISEASES<br/>[FR] DÉRIVÉS DE QUINOLÉINE ET DE QUINOXALINE FLUORÉS UTILISÉS EN TANT QU'INHIBITEURS DE DIHYDROOROTATE DÉSHYDROGÉNASE (DHODH) POUR LE TRAITEMENT DU CANCER, DE MALADIES AUTO-IMMUNES ET INFLAMMATOIRES
    申请人:JANSSEN BIOTECH INC
    公开号:WO2021084500A1
    公开(公告)日:2021-05-06
    The present invention discloses compounds formula (I): (I) wherein X is CH; The present compounds of formula (I) are dihydroorotate dehydrogenase (DHODH) inhibitors, and are useful for the treatment of inflammatory disorders, autoimmune disorders and cancer, such as e.g. lymphomas, leukemias, carcinomas, and sarcomas. The present description discloses the synthesis and characterisation of exemplary compounds as well as pharmacological data thereof (e.g. pages 60 to 136; examples 1 to 39; tables 1 and 2). An exemplary compound is e.g. : 4-ethyl-1-(7-fluoro-4-isopropyl-2- (2-methoxyphenyl)quinolin-6-yl)-3-(hydroxymethyl)-1H-1,2,4- triazol-5(4H)-one (example 1): (AA)
    本发明公开了化合物式(I):(I)其中X为CH;本发明的式(I)化合物是二氢乳酸脱氢酶(DHODH)抑制剂,适用于治疗炎症性疾病、自身免疫性疾病和癌症,例如淋巴瘤、白血病、癌瘤和肉瘤等。本说明公开了示例化合物的合成和表征,以及其药理数据(例如第60至136页;示例1至39;表1和表2)。示例化合物例如为:4-乙基-1-(7-氟-4-异丙基-2-(2-甲氧基苯基)喹啉-6-基)-3-(羟甲基)-1H-1,2,4-三唑-5(4H)-酮(示例1):(AA)
  • Chemokine receptor binding compounds
    申请人:Zhou Yuanxi
    公开号:US20050277668A1
    公开(公告)日:2005-12-15
    The present invention relates to chemokine receptor binding compounds, pharmaceutical compositions and their use. More specifically, the present invention relates to modulators of chemokine receptor activity, preferably modulators of CCR5. These compounds demonstrate protective effects against infection of target cells by a human immunodeficiency virus (HIV).
    本发明涉及趋化因子受体结合化合物、药物组合物及其用途。更具体地,本发明涉及趋化因子受体活性的调节剂,优选为CCR5的调节剂。这些化合物表现出对人类免疫缺陷病毒(HIV)感染靶细胞的保护效果。
  • [EN] BENZIMIDAZOLONE AND BENZOTHIAZOLONE COMPOUNDS AND THEIR USE AS AMPA RECEPTOR MODULATORS<br/>[FR] COMPOSÉS DE BENZIMIDAZOLONE ET DE BENZOTHIAZOLONE ET LEUR UTILISATION COMME MODULATEURS DES RÉCEPTEURS AMPA
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2016176449A1
    公开(公告)日:2016-11-03
    Provided herein are compounds of Formula (I), and pharmaceutically acceptable salts, N-oxides, or solvates thereof, Also provided herein are pharmaceutical compositions comprising compounds of Formula (I) and methods of using compounds of Formula (I).
    本文提供了式(I)的化合物,以及其药用盐、N-氧化物或溶剂化合物。本文还提供了包含式(I)化合物的药物组合物以及使用式(I)化合物的方法。
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