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2-溴-1,3,4-三氟苯 | 176793-04-7

中文名称
2-溴-1,3,4-三氟苯
中文别名
1,3,4-三氟-2-溴苯;2,3,6-三氟溴苯;1,3,4-三氟苯;1-溴-2,3,6-三氟苯
英文名称
2-bromo-1,3,4-trifluorobenzene
英文别名
1-bromo-2,3,6-trifluorobenzene
2-溴-1,3,4-三氟苯化学式
CAS
176793-04-7
化学式
C6H2BrF3
mdl
——
分子量
210.981
InChiKey
CNAXDCSHYHIOGW-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:
    151℃
  • 密度:
    1.758
  • 闪点:
    45℃
  • 稳定性/保质期:
    避氧化物

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xi
  • 危险类别码:
    R36/37/38
  • 海关编码:
    2903999090
  • 安全说明:
    S26,S36/37/39
  • 危险性防范说明:
    P210,P305+P351+P338,P302+P352,P321,P405,P501
  • 危险性描述:
    H315,H319,H335,H227

SDS

SDS:28288669b49bd7e66c85f668c761a7b1
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Material Safety Data Sheet

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

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H301: Toxic if swallowed
P301+P310: IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician

Section 3. Composition/information on ingredients.
Ingredient name: 2-Bromo-1,3,4-trifluorobenzene
CAS number: 176793-04-7

Section 4. First aid measures
Immediately wash skin with copious amounts of water for at least 15 minutes while removing
Skin contact:
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.
Storage: Store in closed vessels.

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
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C6H2BrF3
Molecular weight: 210.98

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, 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
UN Number: UN2811 Class: 6.1 Packing group: III
Proper shipping name: TOXIC SOLIDS, ORGANIC, N.O.S. (2-Bromo-1,3,4-trifluorobenzene)

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:
    2-溴-1,3,4-三氟苯 在 bis(dibenzylideneacetone)-palladium(0) R-(+)-1,1'-联萘-2,2'-双二苯膦sodium t-butanolate 作用下, 以 甲苯 为溶剂, 反应 7.0h, 生成 2-chloro-N-(4-ethylphenyl)-N-(2',3',6'-trifluorophenyl)acetamide
    参考文献:
    名称:
    新型N-芳基羟吲哚的合成作为药理活性化合物的中间体
    摘要:
    合成了各种新的N-芳基羟吲哚作为制备药理活性的2-(N-芳基氨基)-苯乙酸的中间体。除了布赫瓦尔德-芳基化和Smiles重排以外,还探索了两种新颖的方法来构建二芳基胺和N-芳基羟吲哚核心结构。苯胺与2-氧代-环己叉基-乙酸衍生物的缩合反应以及随后的脱氢反应是制备N-芳基羟吲哚的一种新的可行方法。
    DOI:
    10.1016/j.tet.2004.09.064
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文献信息

  • [EN] SUBSTITUTED PIPERIDINE COMPOUND AND USE THEREOF<br/>[FR] COMPOSÉ DE PIPÉRIDINE SUBSTITUÉE ET SON UTILISATION
    申请人:TAKEDA PHARMACEUTICALS CO
    公开号:WO2017135306A1
    公开(公告)日:2017-08-10
    Provided is a substituted piperidine compound having an orexin type 2 receptor agonist activity. A compound represented by the formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof has an orexin type 2 receptor agonist activity, and is useful as a prophylactic or therapeutic agent for narcolepsy.
    提供的是一种替代哌啶化合物,具有促进俐克脑肽2型受体激动剂活性。公式(I)所代表的化合物:其中每个符号如描述中所述,或其盐具有促进俐克脑肽2型受体激动剂活性,并且可用作嗜睡症的预防或治疗药物。
  • [EN] THIENOPYRIDINE CARBOXAMIDES AS UBIQUITIN-SPECIFIC PROTEASE INHIBITORS<br/>[FR] THIÉNOPYRIDINE CARBOXAMIDES UTILISÉS COMME INHIBITEURS DE PROTÉASE SPÉCIFIQUE DE L'UBIQUITINE
    申请人:FORMA THERAPEUTICS INC
    公开号:WO2017139778A1
    公开(公告)日:2017-08-17
    The disclosure relates to inhibitors of USP28 and/or USP25 useful in the treatment of cancers, inflammation, autoimmune diseases, and infectious diseases, having the Formula (I), where R1, R2, R3, R4, R5, R5', R6, R7, X, m, and n are described herein.
    该披露涉及抑制剂USP28和/或USP25,用于治疗癌症、炎症、自身免疫疾病和传染病,具有式(I),其中R1、R2、R3、R4、R5、R5'、R6、R7、X、m和n如本文所述。
  • [EN] SELECTIVE ESTROGEN RECEPTOR MODULATORS FOR THE TREATMENT OF VASOMOTOR SYMPTOMS<br/>[FR] MODULATEURS SELECTIFS DU RECEPTEUR DES OESTROGENES POUR LE TRAITEMENT DE SYMPTOMES VASOMOTEURS
    申请人:LILLY CO ELI
    公开号:WO2005073204A1
    公开(公告)日:2005-08-11
    The present invention relates to a selective estrogen receptor modulator of formula I or Ia: (I) (Ia); or a pharmaceutical acid addition salt thereof; useful for treating vasomotor symptoms, in particular hot flashes, night sweats and other symptoms that affect women around menopause.
    本发明涉及一种公式I或Ia的选择性雌激素受体调节剂:(I) (Ia);或其药物酸加成盐;用于治疗血管舒缩症状,尤其是热潮红、夜间出汗以及影响绝经前后妇女的其他症状。
  • [EN] N-LINKED HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS<br/>[FR] DÉRIVÉS D'ACIDE HYDROXAMIQUE À LIAISON N, UTILES COMME AGENTS ANTIBACTÉRIENS
    申请人:PFIZER
    公开号:WO2011073845A1
    公开(公告)日:2011-06-23
    The present invention is directed to a new class of hydroxamic acid derivatives, their use as LpxC inhibitors, and more specifically their use to treat bacterial infections. Formula (I).
    本发明涉及一类新的羟肟酸衍生物,它们作为LpxC抑制剂的用途,更具体地用于治疗细菌感染。公式(I)。
  • Mild and General Conditions for Negishi Cross-Coupling Enabled by the Use of Palladacycle Precatalysts
    作者:Yang Yang、Nathan J. Oldenhuis、Stephen L. Buchwald
    DOI:10.1002/anie.201207750
    日期:2013.1.7
    A wide range of biaryls were synthesized by palladium‐catalyzed Negishi cross‐couplings at ambient temperature or with low catalyst loading. This protocol features the use of a recently reported aminobiphenyl palladacycle precatalyst to generate the catalytically active XPhosPd0 species. Significantly, a wide range of challenging heterocyclic and polyfluorinated aromatic substrates can be employed
    在环境温度或低催化剂负载量下,通过钯催化的根岸交叉偶联合成了多种联芳基化合物。该协议的特点是使用最近报道的氨基联苯钯环预催化剂来生成具有催化活性的 XPhosPd 0物质。值得注意的是,可以采用各种具有挑战性的杂环和多氟化芳香族底物来获得高产率的产品。
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