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4-乙基环己烯-1-基硼酸 | 871329-72-5

中文名称
4-乙基环己烯-1-基硼酸
中文别名
4-乙基环己烯-1-硼酸
英文名称
(4-ethylcyclohex-1-en-1-yl)boronic acid
英文别名
(4-ethylcyclohexen-1-yl)boronic acid
4-乙基环己烯-1-基硼酸化学式
CAS
871329-72-5
化学式
C8H15BO2
mdl
MFCD07783854
分子量
154.017
InChiKey
NCXGOXGWYXCMKH-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:
    280.2±33.0 °C(Predicted)
  • 密度:
    1.00±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.69
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

SDS

SDS:34ea7f2a45beda1fa91ea083ba672d4f
查看
Material Safety Data Sheet

Section 1. Identification of the substance
4-Ethylcyclohexen-1-ylboronic acid
Product Name:
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H315: Causes skin irritation
H319: Causes serious eye irritation
H335: May cause respiratory irritation
P261: Avoid breathing dust/fume/gas/mist/vapours/spray
Wear protective gloves/protective clothing/eye protection/face protection
P280:
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present
and easy to do – continue rinsing
P304+P340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing
P405: Store locked up

Section 3. Composition/information on ingredients.
4-Ethylcyclohexen-1-ylboronic acid
Ingredient name:
CAS number: 871329-72-5

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.
Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.
Ingestion:

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, under −20◦C.
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
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C8H15BO2
Molecular weight: 154.0

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide.

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-氯-6-三氟甲基烟腈4-乙基环己烯-1-基硼酸四(三苯基膦)钯 、 sodium carbonate 作用下, 以 乙醇甲苯 为溶剂, 生成
    参考文献:
    名称:
    2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides 的 2-烷基/烯基取代的吡啶 C 区类似物作为高效的 TRPV1 拮抗剂。
    摘要:
    研究了一系列 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides 的 2-烷基/烯基吡啶 C 区衍生物作为 hTRPV1 拮抗剂。多种化合物显示出优异的立体特异性 TRPV1 拮抗作用,其效力优于先前的铅 2。其中,化合物 15f 在大鼠神经性疼痛模型中表现出强大的镇痛作用,并以剂量​​依赖性方式阻断辣椒素诱导的体温过低。(S)-15f 与我们的 hTRPV1 同源模型的对接分析提供了对其特定结合模式的深入了解。
    DOI:
    10.1016/j.bmcl.2014.05.074
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文献信息

  • IMIDAZOPYRIDINES AND IMIDAZOPYRAZINES AS LSD1 INHIBITORS
    申请人:Incyte Corporation
    公开号:US20160009712A1
    公开(公告)日:2016-01-14
    The present invention is directed to imidazo[1,5-a]pyridine and imidazo[1,5-a]pyrazine derivatives which are LSD1 inhibitors useful in the treatment of diseases such as cancer.
    本发明涉及咪唑并[1,5-a]吡啶和咪唑并[1,5-a]吡嗪衍生物,这些衍生物是LSD1抑制剂,在治疗癌症等疾病中有用。
  • 2-Alkyl/alkenyl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists
    作者:HyungChul Ryu、Sejin Seo、Seong-Hee Cho、Ho Shin Kim、Aeran Jung、Dong Wook Kang、Karam Son、Minghua Cui、Sun-hye Hong、Pankaz Kumar Sharma、Sun Choi、Peter M. Blumberg、Robert Frank-Foltyn、Gregor Bahrenberg、Hannelore Stockhausen、Klaus Schiene、Thomas Christoph、Sven Frormann、Jeewoo Lee
    DOI:10.1016/j.bmcl.2014.05.074
    日期:2014.8
    A series of 2-alkyl/alkenyl pyridine C-region derivatives of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides were investigated as hTRPV1 antagonists. Multiple compounds showed excellent and stereospecific TRPV1 antagonism with better potency than previous lead 2. Among them, compound 15f demonstrated a strong analgesic profile in a rat neuropathic pain model and blocked capsaicin-induced hypothermia
    研究了一系列 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides 的 2-烷基/烯基吡啶 C 区衍生物作为 hTRPV1 拮抗剂。多种化合物显示出优异的立体特异性 TRPV1 拮抗作用,其效力优于先前的铅 2。其中,化合物 15f 在大鼠神经性疼痛模型中表现出强大的镇痛作用,并以剂量​​依赖性方式阻断辣椒素诱导的体温过低。(S)-15f 与我们的 hTRPV1 同源模型的对接分析提供了对其特定结合模式的深入了解。
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