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(3-溴-5-甲氧基苯基)甲醇 | 262450-64-6

中文名称
(3-溴-5-甲氧基苯基)甲醇
中文别名
3-溴-5-甲氧基苯甲醇
英文名称
(3-bromo-5-methoxyphenyl)methanol
英文别名
——
(3-溴-5-甲氧基苯基)甲醇化学式
CAS
262450-64-6
化学式
C8H9BrO2
mdl
——
分子量
217.062
InChiKey
PPWBDINRNWYVFZ-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2909499000
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335

SDS

SDS:f68e55e753dc08fc42a6410c732fb03e
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: (3-Bromo-5-methoxyphenyl)methanol
Synonyms: 3-Bromo-5-methoxybenzyl alcohol; 3-bromo-5-hydroxymethylanisole

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

Section 3. Composition/information on ingredients.
Ingredient name: (3-Bromo-5-methoxyphenyl)methanol
CAS number: 262450-64-6

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: C8H9BrO2
Molecular weight: 217.1

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

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:
    (3-溴-5-甲氧基苯基)甲醇戴斯-马丁氧化剂 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 生成 3-溴-5-甲氧基苯甲醛
    参考文献:
    名称:
    NOVEL MACROCYCLIC DERIVATIVES, PROCESS FOR PREPARING SAME AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME
    摘要:
    公式(I)的化合物: 其中A1、A2、Ra、Rb、Rc、Rd、R3、R4、X、Y和G按描述中定义, 以及它们在药品制造中的用途。
    公开号:
    US20200253993A1
  • 作为产物:
    描述:
    3-溴-5-甲氧基苯甲醛 在 sodium tetrahydroborate 、 乙醇 作用下, 以 四氢呋喃 为溶剂, 反应 3.0h, 生成 (3-溴-5-甲氧基苯基)甲醇
    参考文献:
    名称:
    8-Substituted isoquinoline derivative and the use thereof
    摘要:
    本发明涉及一种由以下式(1)表示的化合物: 其中D1,A1,D2,R1,D3和R2分别具有与本说明书中定义的相同含义或其盐。由式(1)表示的化合物或其盐具有IKKβ抑制活性等,对于预防和/或治疗IKKβ相关疾病或症状等方面是有用的。
    公开号:
    US20100261701A1
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文献信息

  • Quinolinone derivaties and uses thereof
    申请人:Roche Palo Alto LLC
    公开号:US20040186092A1
    公开(公告)日:2004-09-23
    The invention provides compounds of the formula: 1 and pharmaceutically acceptable salts or prodrugs thereof, wherein m, p, q, r, A, E, X, Y, R 1 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and are as defined herein. The invention also provides methods for preparing, compositions comprising, and methods for using compounds of formula I.
    本发明提供了以下公式的化合物: 1 以及药用可接受的盐或前药,其中m、p、q、r、A、E、X、Y、R 1 ,R 4 ,R 5 ,R 6 ,R 7 ,R 8 ,R 9 如本文所述。本发明还提供了制备公式I化合物的方法、包含这些化合物的组合物以及使用这些化合物的方法。
  • Development of Inhibitors against <i>Mycobacterium abscessus</i> tRNA (m<sup>1</sup>G37) Methyltransferase (TrmD) Using Fragment-Based Approaches
    作者:Andrew J. Whitehouse、Sherine E. Thomas、Karen P. Brown、Alexander Fanourakis、Daniel S.-H. Chan、M. Daben J. Libardo、Vitor Mendes、Helena I. M. Boshoff、R. Andres Floto、Chris Abell、Tom L. Blundell、Anthony G. Coyne
    DOI:10.1021/acs.jmedchem.9b00809
    日期:2019.8.8
    with improved efficacy. tRNA (m1G37) methyltransferase (TrmD) is a promising target for novel antibiotics. It is essential in Mab and other mycobacteria, improving reading frame maintenance on the ribosome to prevent frameshift errors. In this work, a fragment-based approach was employed with the merging of two fragments bound to the active site, followed by structure-guided elaboration to design potent
    脓肿分枝杆菌 (Mab) 是一种快速增长的多重耐药非结核分枝杆菌,对囊性纤维化和其他已有慢性肺部疾病的患者构成越来越大的威胁。单克隆抗体肺部感染很难治疗,有时甚至不可能治疗,会导致肺功能加速衰退和过早死亡。因此,迫切需要开发具有改善功效的新型抗生素。tRNA (m1G37) 甲基转移酶 (TrmD) 是新型抗生素的一个有前景的靶标。它对于 Mab 和其他分枝杆菌至关重要,可改善核糖体上的读码框维护以防止移码错误。在这项工作中,采用基于片段的方法,合并与活性位点结合的两个片段,然后进行结构引导的精加工,以设计针对 Mab TrmD 的有效纳摩尔抑制剂。其中几种化合物对分枝杆菌物种表现出有希望的活性,除了 Mab 之外,还包括结核分枝杆菌和麻风分枝杆菌,支持使用 TrmD 作为开发抗分枝杆菌化合物的靶点。
  • NOVEL MACROCYCLIC DERIVATIVES, PROCESS FOR PREPARING SAME AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME
    申请人:LES LABORATOIRES SERVIER
    公开号:US20200253993A1
    公开(公告)日:2020-08-13
    Compound of formula (I): wherein A 1 , A 2 , R a , R b , R c , R d , R 3 , R 4 , X, Y and G are as defined in the description, and their use in the manufacture of medicaments.
    公式(I)的化合物: 其中A1、A2、Ra、Rb、Rc、Rd、R3、R4、X、Y和G按描述中定义, 以及它们在药品制造中的用途。
  • [EN] IMIDAZOTHIADIAZOLE AND IMIDAZOPYRIDAZINE DERIVATIVES AS PROTEASE ACTIVATED RECEPTOR 4 (PAR4) INHIBITORS FOR TREATING PLATELET AGGREGATION<br/>[FR] DÉRIVÉS D'IMIDAZOTHIADIAZOLE ET D'IMIDAZOPYRIDAZINE UTILES COMME INHIBITEURS DES RÉCEPTEURS 4 ACTIVÉS PAR LES PROTÉASES (PAR4) POUR TRAITER L'AGRÉGATION PLAQUETTAIRE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2013163241A1
    公开(公告)日:2013-10-31
    The present invention provides imidazothiadiazole compounds of Formula (I); Wherein W,Y, R0, R2, R4, Ra, Rb, X1, X2, X3 and X4 are as defined herein,, or a stereoisomer, tautomer, pharmaceutically acceptable salt, prodrug ester or solvate form thereof, wherein all of the variables are as defined herein. These compounds are inhibitors of platelet aggregation and thus can be used as medicaments for treating or preventing thromboembolic disorders.
    本发明提供了公式(I)的咪唑噻二唑化合物;其中W、Y、R0、R2、R4、Ra、Rb、X1、X2、X3和X4如本文所定义,或其立体异构体、互变异构体、药用可接受的盐、前药酯或溶剂化合物形式,其中所有变量如本文所定义。这些化合物是血小板聚集抑制剂,因此可用作治疗或预防血栓栓塞性疾病的药物。
  • Substituted Diphenylethers, -Amines, -Sulfides and -Methanes for the Treatment of Respiratory Disease
    申请人:Bonnert Roger Victor
    公开号:US20080293775A1
    公开(公告)日:2008-11-27
    The invention relates to substituted diphenylethers, -amines, -sulfides, and -methanes as useful pharmaceutical compounds for treating respiratory-disorders, pharmaceutical compositions containing them, and processes for their preparation.
    这项发明涉及替代二苯醚、-胺、-硫化物和-甲烷作为治疗呼吸系统疾病的有用药物化合物,包含它们的药物组合物,以及它们的制备方法。
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