5-溴-2-(二甲基氨基)苯甲醛 | 171881-36-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 5-溴-2-(二甲基氨基)苯甲醛
• 英文名称: 5-bromo-2-(dimethylamino)benzaldehyde
• CAS: 171881-36-0
• 化学式: C₉H₁₀BrNO
• 分子量: 228.088
• InChiKey: KELBDTNCLYIYKB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  20.3
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 海关编码：
  2922399090
• 危险性防范说明：
  P280,P305+P351+P338
• 危险性描述：
  H302

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 5-Bromo-2-(dimethylamino)benzaldehyde
Synonyms:

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

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Section 3. Composition/information on ingredients.
Ingredient name: 5-Bromo-2-(dimethylamino)benzaldehyde
CAS number: 171881-36-0

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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.

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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.

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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.

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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, refrigerated.
Storage:

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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.

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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: C9H10BrNO
Molecular weight: 228.1

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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 bromide.

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Section 11. Toxicological information
No data.

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Section 12. Ecological information
No data.

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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.

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Section 14. Transportation information
Non-harzardous for air and ground transportation.

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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.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  5-溴-2-(二甲基氨基)苯甲醛 在 三乙基硅烷 、 正丁基锂 、 三氟乙酸 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 生成 (3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-[(benzyloxy)methyl]-2-(3-{bicyclo[4.2.0]octa-1(6),2,4-trien-3-ylmethyl}-4-(dimethylamino)phenyl)oxan-2-ol
  参考文献：
  名称：

  苯并环丁烷-C-糖苷作为强效和口服活性SGLT1 / SGLT2双重抑制剂的合成和生物学评估

  摘要：

  描述了作为有效和口服活性的SGLT1 / SGLT2双重抑制剂的苯并环丁烷-C-糖苷的合成和生物学评估。化合物19在SGLT1（IC 50  = 45 nM）上显示出高抑制效能，在SGLT2（IC 50  = 1 nM）上显示出优异的效能。它还在小鼠，大鼠，狗和猴子中表现出出色的PK分布（F  = 78–107％）。在SD大鼠中，化合物19的治疗以剂量依赖性方式显着降低了血糖水平。在ZDF大鼠中，化合物19最多显示24小时的降血糖作用。因此，化合物19可以用作有价值的药理学工具，并且可以潜在地用作代谢综合征的治疗方法。

  DOI：

  10.1016/j.bmcl.2018.02.057
• 作为产物：
  描述：

  2,4-二溴-N-甲基苯胺 在 正丁基锂 、 甲酸 作用下， 以 水 为溶剂， 反应 24.33h， 生成 5-溴-2-(二甲基氨基)苯甲醛
  参考文献：
  名称：

  Stanetty, Peter; Krumpak, Barbara; Rodler, Inge K., Journal of Chemical Research, Miniprint, 1995, # 9, p. 2111 - 2122

  摘要：

  DOI：

文献信息

• [EN] BENZOCYCLOBUTANE DERIVATIVES USEFUL AS DUAL SGLT1/SGLT2 MODULATORS<br/>[FR] DÉRIVÉS DE BENZOCYCLOBUTANE UTILES EN TANT QUE MODULATEURS DOUBLES DE SGLT1/SGLT2
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2018089449A1

  公开（公告）日：2018-05-17

  The present invention is directed to benzocyclobutane derivatives, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions modulated by SGLT activity, more particularly dual SGLT1/2 activity. More particularly, the compounds of the present invention are useful in the treatment of for example, Type II diabetes mellitus, Syndrome X, and complications and symptoms associated with said disorders.

  本发明涉及苯并环丁烷衍生物，含有它们的药物组合物以及它们在治疗由SGLT活性调节的疾病和症状中的应用，更具体地说是双重SGLT1/2活性。更具体地说，本发明的化合物在治疗例如II型糖尿病、X综合征以及与这些疾病相关的并发症和症状中是有用的。
• Redox-Triggered Switchable Synthesis of 3,4-Dihydroquinolin-2(1<i>H</i>)-one Derivatives via Hydride Transfer/<i>N</i>-Dealkylation/<i>N</i>-Acylation
  作者：Xiaoyu Yang、Liang Wang、Fangzhi Hu、Lubin Xu、Sanming Li、Shuai-Shuai Li

  DOI：10.1021/acs.orglett.0c03863

  日期：2021.1.15

  The switchable synthesis of 3-non, 3-mono, 3,3′-disubstituted 3,4-dihydroquinolin-2(1H)-ones was developed through a redox-neutral hydride-transfer/N-dealkylation/N-acylation strategy from o-aminobenzaldehyde with 4-hydroxycoumarin, and Meldrum’s acid, respectively. The unprecedented strategy for the synthesis of 3,3′-highly functionalized 3,4-dihydroquinolin-2(1H)-one has been realized with the in

  通过氧化还原-中性氢化物转移/ N-脱烷基/ N-酰化策略发展了3-非，3-单，3,3'-二取代的3,4-二氢喹啉-2（1 H）-ones的可转换合成分别由邻氨基苯甲醛与4-羟基香豆素和Meldrum酸组成。合成3,3'-高度官能化的3,4-二氢喹啉-2（1 H）-1的空前策略已实现，其中通过迈克尔加成通过o -QM原位利用释放的HCHO 。此外，通过简明合成CYP11B2抑制剂已很好地说明了该方案的合成效用。
• BF₃·OEt₂-Promoted Propargyl Alcohol Rearrangement/[1,5]-Hydride Transfer/Cyclization Cascade Affording Tetrahydroquinolines
  作者：Shuang Zhao、Xiaoyang Wang、Pengfei Wang、Guangwei Wang、Wentao Zhao、Xiangyang Tang、Minjie Guo

  DOI：10.1021/acs.orglett.9b01153

  日期：2019.6.7

  An efficient BF3·OEt2-mediated propargyl alcohol rearrangement/[1,5]-hydride transfer/cyclization cascade for the synthesis of tetrahydroquinoline derivatives has been described. The substituents adjacent to triple bonds play an important role in the formation of ketones (via [1,3]-hydroxyl shift) or alkenyl fluorides which are products of formal trans-carbofluorination of internal alkynes. This method

  已经描述了用于合成四氢喹啉衍生物的有效的BF 3 ·OEt 2介导的炔丙醇重排/ [1,5]-氢化物转移/环化级联反应。与三键相邻的取代基在酮（通过[1,3]-羟基转移）或链烯基氟化物的形成中起着重要作用，它们是内部炔烃的正式反式-碳氟化作用的产物。该方法可以以中等到极好的收率快速访问各种杂环。
• Chiral amino alcohols derived from natural amino acids as chiral solvating agents for carboxylic acids
  作者：Wenge Wang、Xiumin Shen、Fengnian Ma、Zijing Li、Cong Zhang

  DOI：10.1016/j.tetasy.2008.04.030

  日期：2008.5

  Several chiral amino alcohols have been synthesized conveniently and effectively. 1H NMR was utilized to investigate their enantiodiscriminating abilities. Chiral amino alcohols 2 and 4 were discovered as efficient CSAs for the determination of the enantiomeric compositions of chiral carboxylic acids. In particular, for the Ts-derivatives of amino acids studied herein, 4 could be used for the assignment

  方便有效地合成了几种手性氨基醇。1 H NMR用于研究其对映体分辨能力。发现手性氨基醇2和4是测定手性羧酸对映体组成的有效CSAs。特别地，对于本文研究的氨基酸的Ts衍生物，可以使用4通过其NH（Ts ）具有一定信心的质子。
• NOVEL CURCUMIN DERIVATIVE
  申请人：Takahashi Takashi

  公开号：US20100048901A1

  公开（公告）日：2010-02-25

  The present invention provides a novel compound that is structurally similar to curcumin and has a suppressive effect on Aβ aggregation, a degradative effect on Aβ aggregates, an inhibitory effect on β-secretase, and a protective effect on neurons. The novel compound is a compound represented by the following general formula (Ia) or a salt thereof: wherein R 1 represents a 4-hydroxy-3-methoxyphenyl group or the like, and R 2 represents a 1H-indol-6-yl group or the like.

  本发明提供了一种新型化合物，其结构类似于姜黄素，并具有抑制Aβ聚集、降解Aβ聚集体、抑制β-分泌酶以及保护神经元的作用。该新型化合物是由以下通式(Ia)或其盐所表示的化合物：其中，R1表示4-羟基-3-甲氧基苯基或类似基团，R2表示1H-吲哚-6-基基或类似基团。