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1-溴-3-叔丁基-5-甲基苯 | 193905-94-1

中文名称
1-溴-3-叔丁基-5-甲基苯
中文别名
——
英文名称
3-bromo-5-(tert-butyl)toluene
英文别名
1-bromo-3-tert-butyl-5-methyl-benzene;1-Brom-3-tert-butyl-5-methyl-benzol;1-Bromo-3-tert-butyl-5-methylbenzene
1-溴-3-叔丁基-5-甲基苯化学式
CAS
193905-94-1
化学式
C11H15Br
mdl
——
分子量
227.144
InChiKey
VHUIMCRJBRTILQ-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:
    231.5±9.0 °C(Predicted)
  • 密度:
    1.204±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.6
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

安全信息

  • 危险品标志:
    Xi

SDS

SDS:1fb6629b0ddc0a6df7815de372e4c728
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 1-Bromo-3-tert-butyl-5-methylbenzene
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 1-Bromo-3-tert-butyl-5-methylbenzene
CAS number: 193905-94-1

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: C11H15Br
Molecular weight: 227.1

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

反应信息

  • 作为反应物:
    描述:
    4-乙氧羰基苯硼酸1-溴-3-叔丁基-5-甲基苯四(三苯基膦)钯sodium carbonate 作用下, 以 1,4-二氧六环 为溶剂, 反应 24.0h, 以71%的产率得到ethyl 3'‐tert‐butyl‐5'‐methyl‐(1,1'‐biphenyl)‐4‐carboxylate
    参考文献:
    名称:
    A Novel Biphenyl-based Chemotype of Retinoid X Receptor Ligands Enables Subtype and Heterodimer Preferences
    摘要:
    The nuclear retinoid X receptors (RXRs) are key ligand sensing transcription factors that serve as universal nuclear receptor heterodimer partners and are thus involved in numerous physiological processes. Therapeutic targeting of RXRs holds high potential but available RXR activators suffer from limited safety. Selectivity for RXR subtypes or for certain RXR heterodimers are promising strategies for safer RXR modulation. Here, we report systematic structure activity relationship studies on biphenyl carboxylates as new RXR ligand chemotype. We discovered specific structural modifications that enhance potency on RXRs, govern subtype preference, and vary modulation of different RXR heterodimers. Fusion of these structural motifs enabled specific tuning of subtype preferential profiles with markedly improved potency. Our results provide further evidence that RXR subtype selective ligands can be designed and present a novel chemotype of RXR modulators that can be tuned for subtype and heterodimer preferences.
    DOI:
    10.1021/acsmedchemlett.9b00306
  • 作为产物:
    描述:
    氯代异丁烷 、 alkaline earth salt of/the/ methylsulfuric acid 在 三氯化铝 作用下, 生成 1-溴-3-叔丁基-5-甲基苯
    参考文献:
    名称:
    DE86447
    摘要:
    公开号:
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文献信息

  • [EN] CYCLOBUTANE- AND AZETIDINE-CONTAINING MONO AND SPIROCYCLIC COMPOUNDS AS ALPHA V INTEGRIN INHIBITORS<br/>[FR] COMPOSÉS MONO ET SPIROCYCLIQUES CONTENANT DU CYCLOBUTANE ET DE L'AZÉTIDINE EN TANT QU'INHIBITEURS DE L'INTÉGRINE ALPHA V
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2018089355A1
    公开(公告)日:2018-05-17
    The present invention provides compounds of Formula (I): or stereoisomers, tautomers, or pharmaceutically acceptable salts or solvates thereof, wherein all the variables are as defined herein. These compounds are antagonists to αv- containing integrins. This invention also relates to pharmaceutical compositions comprising these compounds and methods of treating a disease, disorder, or condition associated with dysregulation of av-containing integrins, such as pathological fibrosis, transplant rejection, cancer, osteoporosis, and inflammatory disorders, by using the compounds and pharmaceutical compositions.
    本发明提供了式(I)的化合物:或其立体异构体、互变异构体或药学上可接受的盐或溶剂,其中所有变量如本文所定义。这些化合物是αv-含有整合素的拮抗剂。本发明还涉及包括这些化合物的药物组合物以及利用这些化合物和药物组合物治疗与αv-含有整合素失调相关的疾病、紊乱或病况的方法,如病理性纤维化、移植排斥、癌症、骨质疏松症和炎症性疾病。
  • [EN] AZOLE AMIDES AND AMINES AS ALPHA V INTEGRIN INHIBITORS<br/>[FR] AMIDES D'AZOLE ET AMINES EN TANT QU'INHIBITEURS D'INTÉGRINE ALPHA V
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2018089358A1
    公开(公告)日:2018-05-17
    The present invention provides compounds of Formula (I): (Formula (I)), or stereoisomers, tautomers, or pharmaceutically acceptable salts or solvates thereof, wherein all the variables are as defined herein. These compounds are inhibitors to αv-containing integrins. This invention also relates to pharmaceutical compositions comprising these compounds and methods of treating a disease, disorder, or condition associated with dysregulation of αv-containing integrins, such as pathological fibrosis, transplant rejection, cancer, osteoporosis, and inflammatory disorders, by using the compounds and pharmaceutical compositions.
    本发明提供了Formula (I)的化合物:(Formula (I)),或其立体异构体、互变异构体、或其药学上可接受的盐或溶剂化合物,其中所有变量如本文所定义。这些化合物是αv-含有整合素的抑制剂。本发明还涉及包括这些化合物的药物组合物以及利用这些化合物和药物组合物治疗与αv-含有整合素失调相关的疾病、紊乱或症状,如病理纤维化、移植排斥、癌症、骨质疏松症和炎症性疾病的方法。
  • [EN] PYRROLE AMIDES AS ALPHA V INTEGRIN INHIBITORS<br/>[FR] AMIDES DE PYRROLE EN TANT QU'INHIBITEURS D'INTÉGRINE ALPHA V
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2018089360A1
    公开(公告)日:2018-05-17
    The present invention provides compounds of Formula (I) or stereoisomers, tautomers, or pharmaceutically acceptable salts or solvates thereof, wherein all the variables are as defined herein. These compounds are inhibitors to αv-containing integrins. This invention also relates to pharmaceutical compositions comprising these compounds and methods of treating a disease, disorder, or condition associated with dysregulation of αv-containing integrins, such as pathological fibrosis, transplant rejection, cancer, osteoporosis, and inflammatory disorders, by using the compounds and pharmaceutical compositions.
    本发明提供了具有式(I)的化合物或其立体异构体、互变异构体、或其药用可接受的盐或溶剂,其中所有变量均如本文所定义。这些化合物是αv-含有整合素的抑制剂。本发明还涉及包含这些化合物的药物组合物以及利用这些化合物和药物组合物治疗与αv-含有整合素失调相关的疾病、紊乱或病况的方法,例如病理纤维化、移植排斥、癌症、骨质疏松症和炎症性疾病。
  • HETEROCYCLIC ANTIVIRAL COMPOUNDS
    申请人:Steiner Sandra
    公开号:US20100158860A1
    公开(公告)日:2010-06-24
    Compounds having the formula I wherein A, R 1 , R 2 , R 3 , R 4a , R 4b , R 4c , R 5 , R 6 , R 7a , R 7b , Ar 1 , R c , R d , R e , R f , X, n and p are as defined herein are Hepatitis C virus NS5b polymerase inhibitors. Also disclosed are compositions and methods for treating an HCV infection and inhibiting HCV replication.
    具有以下公式I的化合物,在该公式中A、R1、R2、R3、R4a、R4b、R4c、R5、R6、R7a、R7b、Ar1、Rc、Rd、Re、Rf、X、n和p的定义如本文所述,是丙型肝炎病毒NS5b聚合酶抑制剂。还公开了用于治疗HCV感染和抑制HCV复制的组合物和方法。
  • [EN] 3-SUBSTITUTED PROPIONIC ACIDS AS ALPHA V INTEGRIN INHIBITORS<br/>[FR] ACIDES PROPIONIQUES À SUBSTITUTION EN POSITION 3 EN TANT QU'INHIBITEURS D'INTÉGRINE ALPHA V
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2018089353A1
    公开(公告)日:2018-05-17
    The present invention provides compounds of Formula (I): or stereoisomers, tautomers, or pharmaceutically acceptable salts or solvates thereof, wherein all the variables are as defined herein. These compounds are antagonists to αν- containing integrins. This invention also relates to pharmaceutical compositions comprising these compounds and methods of treating a disease, disorder, or condition associated with dysregulation of ay- containing integrins, such as pathological fibrosis, transplant rejection, cancer, osteoporosis, and inflammatory disorders, by using the compounds and pharmaceutical compositions.
    本发明提供了化合物的公式(I):或其立体异构体、互变异构体或药学上可接受的盐或溶剂,其中所有变量如本文所定义。这些化合物是αν-含有整合素的拮抗剂。本发明还涉及包含这些化合物的药物组合物和使用这些化合物和药物组合物来治疗与ay-含有整合素失调相关的疾病、疾病或症状的方法,例如病理纤维化、移植排斥、癌症、骨质疏松症和炎症性疾病。
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