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5-溴-2-氯-3-甲醛吡啶 | 228251-24-9

中文名称
5-溴-2-氯-3-甲醛吡啶
中文别名
5-溴-2-氯-3-甲酰吡啶;2-氯-5-溴-3-吡啶甲醛;2-氯-5-溴-烟醛;5-溴-2-氯烟醛
英文名称
5-bromo-2-chloronicotinaldehyde
英文别名
5-bromo-2-chloropyridine-3-carbaldehyde
5-溴-2-氯-3-甲醛吡啶化学式
CAS
228251-24-9
化学式
C6H3BrClNO
mdl
——
分子量
220.453
InChiKey
YGPYNLZCNDPHTQ-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:
    278.0±35.0 °C(Predicted)
  • 密度:
    1.800±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    30
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi
  • 海关编码:
    2933399090
  • WGK Germany:
    3
  • 危险标志:
    GHS06
  • 危险性描述:
    H301
  • 危险性防范说明:
    P301 + P310
  • 储存条件:
    温度:2-8°C,保持在惰性气体氛围中。

SDS

SDS:cc42c42fefdc4c6cda962aed1b2afb4d
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SECTION 1: Identification of the substance/mixture and of the company/undertaking
Product identifiers
Product name : 5-Bromo-2-Chloro-Pyridine-3-Carbaldehyde
REACH No. : A registration number is not available for this substance as the substance
or its uses are exempted from registration, the annual tonnage does not
require a registration or the registration is envisaged for a later
registration deadline.
Relevant identified uses of the substance or mixture and uses advised against
Identified uses : Laboratory chemicals, Manufacture of substances



SECTION 2: Hazards identification
Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008
Acute toxicity, Oral (Category 3), H301
For the full text of the H-Statements mentioned in this Section, see Section 16.
Classification according to EU Directives 67/548/EEC or 1999/45/EC
T Toxic R25
For the full text of the R-phrases mentioned in this Section, see Section 16.
Label elements
Labelling according Regulation (EC) No 1272/2008
Pictogram
Signal word Danger
Hazard statement(s)
H301 Toxic if swallowed.
Precautionary statement(s)
P301 + P310 IF SWALLOWED: Immediately call a POISON CENTER or doctor/
physician.
Supplemental Hazard none
Statements
Other hazards
This substance/mixture contains no components considered to be either persistent, bioaccumulative and
toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher.

SECTION 3: Composition/information on ingredients
Substances
Molecular weight : 220,45 g/mol
Hazardous ingredients according to Regulation (EC) No 1272/2008
Component Classification Concentration
5-Bromo-2-Chloro-Pyridine-3-Carbaldehyde
Acute Tox. 3; H301 <= 100 %
Hazardous ingredients according to Directive 1999/45/EC
Component Classification Concentration
5-Bromo-2-Chloro-Pyridine-3-Carbaldehyde
T, R25 <= 100 %
For the full text of the H-Statements and R-Phrases mentioned in this Section, see Section 16

SECTION 4: First aid measures
Description of first aid measures
General advice
Consult a physician. Show this safety data sheet to the doctor in attendance.
If inhaled
If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician.
In case of skin contact
Wash off with soap and plenty of water. Take victim immediately to hospital. Consult a physician.
In case of eye contact
Flush eyes with water as a precaution.
If swallowed
Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.
Most important symptoms and effects, both acute and delayed
The most important known symptoms and effects are described in the labelling (see section 2.2) and/or in
section 11
Indication of any immediate medical attention and special treatment needed
No data available

SECTION 5: Firefighting measures
Extinguishing media
Suitable extinguishing media
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Nature of decomposition products not known.
Advice for firefighters
Wear self-contained breathing apparatus for firefighting if necessary.
Further information
No data available

SECTION 6: Accidental release measures
Personal precautions, protective equipment and emergency procedures
Wear respiratory protection. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure
adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust.
For personal protection see section 8.
Environmental precautions
Prevent further leakage or spillage if safe to do so. Do not let product enter drains.
Methods and materials for containment and cleaning up
Pick up and arrange disposal without creating dust. Sweep up and shovel. Keep in suitable, closed
containers for disposal.
Reference to other sections
For disposal see section 13.

SECTION 7: Handling and storage
Precautions for safe handling
Avoid contact with skin and eyes. Avoid formation of dust and aerosols.
Provide appropriate exhaust ventilation at places where dust is formed.
For precautions see section 2.2.
Conditions for safe storage, including any incompatibilities
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
Storage class (TRGS 510): Non-combustible, acute toxic Cat.3 / toxic hazardous materials or hazardous
materials causing chronic effects
Specific end use(s)
Apart from the uses mentioned in section 1.2 no other specific uses are stipulated

SECTION 8: Exposure controls/personal protection
Control parameters
Components with workplace control parameters
Exposure controls
Appropriate engineering controls
Avoid contact with skin, eyes and clothing. Wash hands before breaks and immediately after handling
the product.
Personal protective equipment
Eye/face protection
Face shield and safety glasses Use equipment for eye protection tested and approved under
appropriate government standards such as NIOSH (US) or EN 166(EU).
Skin protection
Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique
(without touching glove's outer surface) to avoid skin contact with this product. Dispose of
contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.
The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and
the standard EN 374 derived from it.
Body Protection
Complete suit protecting against chemicals, The type of protective equipment must be selected
according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection
Where risk assessment shows air-purifying respirators are appropriate use a full-face particle
respirator type N99 (US) or type P2 (EN 143) respirator cartridges as a backup to engineering
controls. If the respirator is the sole means of protection, use a full-face supplied air respirator. Use
respirators and components tested and approved under appropriate government standards such
as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so. Do not let product enter drains.

SECTION 9: Physical and chemical properties
Information on basic physical and chemical properties
a) Appearance Form: solid
b) Odour No data available
c) Odour Threshold No data available
d) pH No data available
e) Melting point/freezing No data available
point
f) Initial boiling point and No data available
boiling range
g) Flash point No data available
h) Evaporation rate No data available
i) Flammability (solid, gas) No data available
j) Upper/lower No data available
flammability or
explosive limits
k) Vapour pressure No data available
l) Vapour density No data available
m) Relative density No data available
n) Water solubility No data available
o) Partition coefficient: n- No data available
octanol/water
p) Auto-ignition No data available
temperature
q) Decomposition No data available
temperature
r) Viscosity No data available
s) Explosive properties No data available
t) Oxidizing properties No data available
Other safety information
No data available

SECTION 10: Stability and reactivity
Reactivity
No data available
Chemical stability
Stable under recommended storage conditions.
Possibility of hazardous reactions
No data available
Conditions to avoid
No data available
Incompatible materials
Strong oxidizing agents
Hazardous decomposition products
In the event of fire: see section 5

SECTION 11: Toxicological information
Information on toxicological effects
Acute toxicity
No data available
Skin corrosion/irritation
No data available
Serious eye damage/eye irritation
No data available
Respiratory or skin sensitisation
No data available
Germ cell mutagenicity
No data available
Carcinogenicity
IARC: No component of this product present at levels greater than or equal to 0.1% is identified as
probable, possible or confirmed human carcinogen by IARC.
Reproductive toxicity
No data available
Specific target organ toxicity - single exposure
No data available
Specific target organ toxicity - repeated exposure
No data available
Aspiration hazard
No data available
Additional Information
RTECS: Not available
To the best of our knowledge, the chemical, physical, and toxicological properties have not been
thoroughly investigated.

SECTION 12: Ecological information
Toxicity
No data available
Persistence and degradability
No data available
Bioaccumulative potential
No data available
Mobility in soil
No data available
Results of PBT and vPvB assessment
This substance/mixture contains no components considered to be either persistent, bioaccumulative and
toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher.
Other adverse effects
No data available

SECTION 13: Disposal considerations
Waste treatment methods
Product
Offer surplus and non-recyclable solutions to a licensed disposal company. Dissolve or mix the material
with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber.
Contaminated packaging
Dispose of as unused product.

SECTION 14: Transport information
UN number
ADR/RID: - IMDG: - IATA: -
UN proper shipping name
ADR/RID: Not dangerous goods
IMDG: Not dangerous goods
IATA: Not dangerous goods
Transport hazard class(es)
ADR/RID: - IMDG: - IATA: -
Packaging group
ADR/RID: - IMDG: - IATA: -
Environmental hazards
ADR/RID: no IMDG Marine pollutant: no IATA: no
Special precautions for user
No data available

SECTION 15: Regulatory information
This safety datasheet complies with the requirements of Regulation (EC) No. 1907/2006.
Safety, health and environmental regulations/legislation specific for the substance or mixture
No data available
Chemical Safety Assessment
For this product a chemical safety assessment was not carried out

SECTION 16: Other information
Full text of H-Statements referred to under sections 2 and 3.
Acute Tox. Acute toxicity
H301 Toxic if swallowed.
Full text of R-phrases referred to under sections 2 and 3
T Toxic
R25 Toxic if swallowed.
Further information
Copyright 2014 Co. LLC. License granted to make unlimited paper copies for internal use
only.
The above information is believed to be correct but does not purport to be all inclusive and shall be
used only as a guide. The information in this document is based on the present state of our knowledge
and is applicable to the product with regard to appropriate safety precautions. It does not represent any
guarantee of the properties of the product. Corporation and its Affiliates shall not be held
liable for any damage resulting from handling or from contact with the above product. See
and/or the reverse side of invoice or packing slip for additional terms and conditions of sale.

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:
    5-溴-2-氯-3-甲醛吡啶1,2,3,4,5,6,7,8-八硫杂环辛烷硫酸氢铵potassium phosphate 作用下, 以 二甲基亚砜 为溶剂, 反应 15.0h, 以58%的产率得到5-bromoisothiazolo[5,4-b]pyridine
    参考文献:
    名称:
    一种苯并异噻唑类化合物及其制备方法
    摘要:
    本发明公开一种苯并异噻唑类化合物及其制备方法,苯并异噻唑类化合物的制备方法是在碱存在、反应温度为80~150℃下,芳香醛类化合物与硫粉、无机铵盐一步反应生成苯并异噻唑类化合物。本发明在较为温和条件下实现了苯并异噻唑环的一步合成,反应对空气及水兼容,具有步骤简单、成本低,操作简单等优点,具有很好的应用前景。
    公开号:
    CN113214182B
  • 作为产物:
    描述:
    5-溴-2-氯烟酸 在 lithium aluminium tetrahydride 、 氯化亚砜 作用下, 以 四氢呋喃 为溶剂, 反应 21.0h, 生成 5-溴-2-氯-3-甲醛吡啶
    参考文献:
    名称:
    [EN] HPK1 ANTAGONISTS AND USES THEREOF
    [FR] ANTAGONISTES DE HPK1 ET LEURS UTILISATIONS
    摘要:
    本发明提供了化合物,其组成物以及使用它们来抑制HPK1和治疗HPK1介导的疾病的方法。
    公开号:
    WO2022187856A1
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文献信息

  • [EN] SULFONAMIDE COMPOUNDS HAVING TNAP INHIBITORY ACTIVITY<br/>[FR] COMPOSÉS DE SULFONAMIDE AYANT UNE ACTIVITÉ INHIBITRICE DE TNAP
    申请人:DAIICHI SANKYO CO LTD
    公开号:WO2018119444A1
    公开(公告)日:2018-06-28
    The present invention relates to a compound or a pharmacologically acceptable salt thereof having excellent tissue non-specific alkaline phosphatase inhibitory activity. The present invention provides a compound represented by the formula (I) or a pharmacologically acceptable salt thereof.
    本发明涉及一种具有优异的组织非特异性碱性磷酸酶抑制活性的化合物或其药理学上可接受的盐。本发明提供一种由式(I)表示的化合物或其药理学上可接受的盐。
  • [EN] PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII<br/>[FR] MACROCYCLES PEPTIDIQUES CONTRE ACINETOBACTER BAUMANNII
    申请人:HOFFMANN LA ROCHE
    公开号:WO2017072062A1
    公开(公告)日:2017-05-04
    The present invention provides compounds of formula (I) wherein X1 to X8 and R1 to R8 are as described herein, as well as pharmaceutically acceptable salts thereof. Further the present invention is concerned with the manufacture of the compounds of formula (I), pharmaceutical compositions comprising them and their use as medicaments for the treatment of diseases and infections caused by Acinetobacter baumannii.
    本发明提供了式(I)的化合物,其中X1至X8和R1至R8如本文所述,以及其药学上可接受的盐。此外,本发明涉及制备式(I)的化合物,包括它们的药物组合物以及它们作为治疗由鲍曼不动杆菌引起的疾病和感染的药物的用途。
  • HPK1 ANTAGONISTS AND USES THEREOF
    申请人:Nimbus Saturn, Inc.
    公开号:US20210078996A1
    公开(公告)日:2021-03-18
    The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of HPK1, and the treatment of HPK1-mediated disorders.
    本发明提供了化合物、其组合物以及使用这些化合物用于抑制HPK1和治疗HPK1介导的疾病的方法。
  • Bicyclic sulfonamide compounds as sodium channel inhibitors
    申请人:AMGEN INC.
    公开号:US09212182B2
    公开(公告)日:2015-12-15
    The present invention provides compounds of Formula I, and pharmaceutically acceptable salts thereof, that are inhibitors of voltage-gated sodium channels, in particular Nav1.7. The compounds are useful for the treatment of diseases associated with the activity of sodium channels such as pain disorders and itch. Also provided are pharmaceutical compositions containing compounds of the present invention.
    本发明提供了式I的化合物及其药学上可接受的盐,这些化合物是钠通道的抑制剂,特别是Nav1.7。这些化合物对于治疗与钠通道活性相关的疾病,如疼痛障碍和瘙痒,是有用的。还提供了含有本发明化合物的药物组合物。
  • Sulfonamides as Selective Na<sub>V</sub>1.7 Inhibitors: Optimizing Potency, Pharmacokinetics, and Metabolic Properties to Obtain Atropisomeric Quinolinone (AM-0466) that Affords Robust in Vivo Activity
    作者:Russell F. Graceffa、Alessandro A. Boezio、Jessica Able、Steven Altmann、Loren M. Berry、Christiane Boezio、John R. Butler、Margaret Chu-Moyer、Melanie Cooke、Erin F. DiMauro、Thomas A. Dineen、Elma Feric Bojic、Robert S. Foti、Robert T. Fremeau、Angel Guzman-Perez、Hua Gao、Hakan Gunaydin、Hongbing Huang、Liyue Huang、Christopher Ilch、Michael Jarosh、Thomas Kornecook、Charles R. Kreiman、Daniel S. La、Joseph Ligutti、Benjamin C. Milgram、Min-Hwa Jasmine Lin、Isaac E. Marx、Hanh N. Nguyen、Emily A. Peterson、Gwen Rescourio、John Roberts、Laurie Schenkel、Roman Shimanovich、Brian A. Sparling、John Stellwagen、Kristin Taborn、Karina R. Vaida、Jean Wang、John Yeoman、Violeta Yu、Dawn Zhu、Bryan D. Moyer、Matthew M. Weiss
    DOI:10.1021/acs.jmedchem.6b01850
    日期:2017.7.27
    genetic validation, NaV1.7 has attracted significant interest as a target for the treatment of pain. We have previously reported on a number of structurally distinct bicyclic heteroarylsulfonamides as NaV1.7 inhibitors that demonstrate high levels of selectivity over other NaV isoforms. Herein, we report the discovery and optimization of a series of atropisomeric quinolinone sulfonamide inhibitors [Bicyclic
    由于其强大的遗传学验证,Na V 1.7作为治疗疼痛的靶标引起了人们的极大兴趣。我们以前曾报道过许多结构上不同的双环杂芳基磺酰胺盐,它们是Na V 1.7抑制剂,与其他Na V同工型相比,具有较高的选择性。在此,我们报告了一系列阻转异构的喹啉酮磺酰胺抑制剂[双环磺酰胺化合物作为钠通道抑制剂]的发现和优化及其制备方法。WO 2014201206, 2014]的Na V 1.7,这表明的Na纳摩尔抑制V 1.7和比其他钠通道亚型表现出高水平的选择性。在优化了包括PXR活化,CYP2C9抑制和CYP3A4 TDI在内的代谢和药代动力学特性后,将几种化合物推入了体内靶标参与和功效模型。在小鼠中进行测试时,化合物39(AM-0466)在组胺诱导的瘙痒性Na V 1.7依赖性模型(瘙痒)中以及在辣椒素诱导的痛觉伤害模型中均表现出强大的药效学活性,而在开腹中没有任何混淆作用现场活动。
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