2,3-二溴苯酚 | 57383-80-9

• 物质功能分类: 有机原料 - 醇、酚、酚醇类化合物及衍生物 - 酚及其卤化、磺化、硝化或亚硝化衍生物
• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 中文名称: 2,3-二溴苯酚
• 英文名称: 2,3-dibromophenol
• CAS: 57383-80-9
• 化学式: C₆H₄Br₂O
• 分子量: 251.905
• InChiKey: FNAKEOXYWBWIRT-UHFFFAOYSA-N

物化性质

• 熔点：
  68-69 °C
• 沸点：
  252.1±20.0 °C(Predicted)
• 密度：
  2.095±0.06 g/cm3(Predicted)
• 溶解度：
  可溶于氯仿（少许）、甲醇（少许）

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：
  0.0
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

安全信息

• 海关编码：
  2908199090
• 储存条件：
  2-8°C

SDS

Material Safety Data Sheet

---

Section 1. Identification of the substance
Product Name: 2,3-Dibromophenol
Synonyms:

---

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

---

Section 3. Composition/information on ingredients.
Ingredient name: 2,3-Dibromophenol
CAS number: 57383-80-9

---

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: C6H4Br2O
Molecular weight: 251.9

---

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：

  2,3-二溴苯酚 在 盐酸 、 sodium hydroxide 作用下， 以 乙醇 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 5.0h， 生成 2,3-二溴苯甲醚
  参考文献：
  名称：

  2,3-二卤代苯胺的合成方法。4-功能化-1 H-吲哚的有用前体

  摘要：

  已经证明2，3-二卤代苯胺是用于合成4-卤代-1 H-吲哚的有用的起始原料。所制备的卤代吲哚的随后或原位官能化使得能够以良好的总收率获得各种2,4-或2,3,4-区域选择性官能化的吲哚。由于在文献中没有描述制备2，3-二卤代苯胺的有效合成途径，因此现在提出了制备这些1,2,3-官能化的芳族前体的不同方法。最一般的涉及从相应的2，3-二卤代苯酚的Smiles重排，并允许以直接且合成上有用的方式制备2，3-二卤代苯胺。

  DOI：

  10.1021/jo200406f
• 作为产物：
  描述：

  1,2-二溴苯 在 叔丁基过氧化氢 、 copper acetylacetonate 作用下， 以 水 为溶剂， 反应 12.0h， 以95%的产率得到2,3-二溴苯酚
  参考文献：
  名称：

  一种2,3-二溴苯酚或其衍生物的高效合成方法

  摘要：

  本发明涉及一种2,3‑二溴苯酚或其衍生物的高效合成方法，该方法为：将邻二溴苯或邻二溴苯衍生物、过氧叔丁醇加入至水中，并加入铜催化剂，之后在室温下反应6‑12小时，经分离纯化即得到2,3‑二溴苯酚或2,3‑二溴苯酚衍生物。与现有技术相比，本发明合成工艺简单绿色，具有优良的选择性和较高产率，且反应后处理简单，以水为溶剂环保安全。本发明在药物合成、天然产物等的合成中有很大的应用潜力。

  公开号：

  CN110981702B

文献信息

• 一种含氮杂七元环衍生物的化合物、制备方法及其在有机电致发光器件上的应用
  申请人：江苏三月光电科技有限公司

  公开号：CN109574931A

  公开（公告）日：2019-04-05

  本发明公开了一种含氮杂七元环衍生物的化合物、制备方法及其在有机电致发光器件上的应用，属于半导体技术领域。本发明提供的有机化合物的结构如通式(1)所示：本发明还公开了上述化合物的制备方法及其在有机电致发光器件上的应用。本发明提供的本发明化合物具有较高的玻璃化温度和分子热稳定性，合适的HOMO和LUMO能级，较高Eg，通过器件结构优化，可有效提升OLED器件的光电性能以及OLED器件的寿命。
• [EN] HETEROCYCLIC COMPOUNDS WITH AN ROR(GAMMA)T MODULATING ACTIVITY<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES AYANT UNE ACTIVITÉ DE MODULATION DE ROR(GAMMA)T
  申请人：TAKEDA PHARMACEUTICALS CO

  公开号：WO2018030550A1

  公开（公告）日：2018-02-15

  The present invention relates to a compound that may have an ROR(gamma)t modulating activity and can thus be useful in the treatment of cancer.

  本发明涉及一种可能具有ROR(gamma)t调节活性的化合物，因此可用于癌症治疗。
• [EN] TYK-2 INHIBITOR<br/>[FR] INHIBITEUR DE TYK -2
  申请人：BEIGENE LTD

  公开号：WO2021259208A1

  公开（公告）日：2021-12-30

  Disclosed herein is a compound of Formula (I) for inhibiting TYK2 and treating a disease associated with the undesirable tyk-2 activity (tyk-2 related diseases), a method of using the compounds disclosed herein for treating inflammatory or autoimmune disease, and a pharmaceutical composition comprising the same.

  本发明公开了一种式I化合物，用于抑制TYK2并治疗与不良tyk-2活性相关的疾病（tyk-2相关疾病），使用本发明所述化合物治疗炎症或自身免疫疾病的方法，以及包含所述化合物的药物组合物。
• Regioselectivity of Diels–Alder reactions between 6,7-dehydrobenzofuran and 2-substituted furans
  作者：Neil Brown、Keith R. Buszek

  DOI：10.1016/j.tetlet.2012.05.118

  日期：2012.8

  via metal–halogen exchange and elimination, in a manner similar to our previous work with 6,7-indole arynes. This benzofuranyne undergoes highly regioselective Diels–Alder cycloadditions with 2-substituted furans.

  我们描述了通过金属 - 卤素交换和消除从 6,7-二卤代苯并呋喃生成 6,7-脱氢苯并呋喃（6,7-苯并呋喃）的第一份报告，其方式类似于我们之前使用 6,7-吲哚芳烃的工作. 这种苯并呋喃与 2-取代呋喃发生高度区域选择性的 Diels-Alder 环加成反应。
• A New and Efficient Synthesis of 4-Functionalized Benzo[<i>b</i>]furans from 2,3-Dihalophenols
  作者：Roberto Sanz、M. Pilar Castroviejo、Yolanda Fernández、Francisco J. Fañanás

  DOI：10.1021/jo0508402

  日期：2005.8.1

  Tandem Sonogashira coupling/5-endo-dig cyclization reactions on 2,3-dihalophenols suppose a straightforward entry to 4-halobenzo[b]furans, which can be easily transformed into 4-functionalized benzo[b]furans, that are difficult to synthesize by other procedures. On the other hand, the starting 2,3-dihalophenols are efficiently prepared from commercially available 3-halophenols, via their N,N-diethyl

  串联Sonogashira偶联/ 5-内切-挖上-2,3- dihalophenols环化反应假设一个简单的项，以4- halobenzo [ b ]呋喃，其可以容易地转化为4 -官能化苯并[ b ]呋喃，难以合成通过其他程序。另一方面，起始的2,3-二卤代苯酚是由市售的3-卤代苯酚经其N，N-二乙基氨基甲酸酯通过在低位用s -BuLi / TMEDA或LDA处理在2-位选择性锂化而有效制备的。温度和与卤素亲电子试剂的反应。