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2-甲基吡啶-4-硼酸频哪酯 | 660867-80-1

中文名称
2-甲基吡啶-4-硼酸频哪酯
中文别名
2-甲基-4-吡啶硼酸频那醇酯;2-甲基吡啶-4-硼酸频哪酯,95%;2-甲基-4-吡啶硼酸频呐醇酯;2-甲基吡啶-4-硼酸频哪醇酯
英文名称
2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
英文别名
2-methylpyridine-4-boronic acid pinacol ester;2-methyl-4-pyridine boronic acid pinacol ester
2-甲基吡啶-4-硼酸频哪酯化学式
CAS
660867-80-1
化学式
C12H18BNO2
mdl
——
分子量
219.091
InChiKey
MBTULFIFECUURA-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

  • 熔点:
    66-71°C
  • 沸点:
    315.9±30.0 °C(Predicted)
  • 密度:
    1.02
  • 溶解度:
    溶于甲醇
  • 稳定性/保质期:
    按规定使用和贮存的不会分解,避免与氧化物接触。

计算性质

  • 辛醇/水分配系数(LogP):
    1.69
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    31.4
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xi
  • 安全说明:
    S26,S39
  • 危险类别码:
    R37/38,R41
  • 海关编码:
    2934999090
  • 危险性防范说明:
    P280,P305+P351+P338,P310
  • 危险性描述:
    H302,H315,H319,H332,H335

SDS

SDS:c604abcf6da4a1af2bf24b2f1bb00599
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2-Methylpyridine-4-boronic acid pinacol ester
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H315: Causes skin irritation
H318: Causes serious eye damage
H335: May cause respiratory irritation
P261: Avoid breathing dust/fume/gas/mist/vapours/spray
P280: Wear protective gloves/protective clothing/eye protection/face protection
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present
and easy to do – continue rinsing

Section 3. Composition/information on ingredients.
Ingredient name: 2-Methylpyridine-4-boronic acid pinacol ester
CAS number: 660867-80-1

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, 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
Appearance: Not specified
No data
Boiling point:
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C12H18BNO2
Molecular weight: 219.1

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.

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

上下游信息

  • 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:
    2-甲基吡啶-4-硼酸频哪酯sodium periodate 、 ammonium acetate 作用下, 以 丙酮 为溶剂, 反应 12.0h, 生成 2-甲基-4-吡啶硼酸
    参考文献:
    名称:
    [EN] DERIVATIVES OF 2-TRIFLUORMETHYL-6-AMINOPURINE AS PHOSPHODIESTERASE 4 INHIBITORS
    [FR] INHIBITEURS DE LA PHOSPHODIESTERASE 4
    摘要:
    公开号:
    WO2004014913A3
  • 作为产物:
    描述:
    碳酸甲丙酯联硼酸频那醇酯 在 (1,5-cyclooctadiene)(methoxy)iridium(I) dimer 、 4,4'-二叔丁基-2,2'-二吡啶 、 C32H49AlBr2O2 作用下, 以 正己烷 为溶剂, 反应 6.5h, 以65%的产率得到2-甲基吡啶-4-硼酸频哪酯
    参考文献:
    名称:
    铱/铝协同催化对(杂)烯进行对映选择性C-H硼化
    摘要:
    苯甲酰胺和吡啶的对位C-H硼化已通过铱/铝协同催化实现。芳烃CH硼化中常用的铱催化剂和庞大的铝基路易斯酸催化剂的结合提供了一种空前的策略,可控制CH硼化的区域选择性,从而得到各种取代的(杂)芳基硼酸酯,它们是复杂的多用途合成中间体多取代的芳族化合物。
    DOI:
    10.1002/anie.201701238
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文献信息

  • [EN] NOVEL COMPOUNDS<br/>[FR] NOUVEAUX COMPOSÉS
    申请人:INFLAZOME LTD
    公开号:WO2019211463A1
    公开(公告)日:2019-11-07
    The present invention relates to substituted 5-membered nitrogen containing heteroaryl compounds, such as sulfonyl triazoles, where the heteroaryl ring is further substituted, optionally via a linking group such as -NH-, with a cyclic group which in turn is substituted at the α-position. The present invention further relates to associated salts, solvates, prodrugs and pharmaceutical compositions, and to the use of such compounds in the treatment and prevention of medical disorders and diseases, most especially by NLRP3 inhibition.
    本发明涉及取代的含氮杂环化合物,例如磺酰基三唑,其中杂环环进一步取代,可选地通过类似-NH-的连接基团,与环状基团相连,该环状基团在α-位置进一步取代。本发明还涉及相关的盐、溶剂合物、前药和药物组合物,以及这些化合物在治疗和预防医学疾病和疾病中的使用,尤其是通过NLRP3抑制。
  • 具有Wnt信号通路抑制活性的杂环化合物
    申请人:苏州云轩医药科技有限公司
    公开号:CN104557862B
    公开(公告)日:2017-05-17
    本发明涉及一种具有Wnt信号通路抑制活性的杂环化合物,包括该化合物及其药学上可接受的盐、各种同位素、各种异构体或各种晶型结构,具有通式I所示的结构:本发明所涉及的化合物及其联合应用组合物可以有效抑制Wnt信号通路,能够用于治疗或预防与Wnt信号通路相关的病症。
  • [EN] AMINO PYRAZINE DERIVATIVES AS PHOSPHATIDYLINOSITOL 3-KINASE INHIBITORS<br/>[FR] DÉRIVÉS AMINÉS DE PYRAZINE UTILISABLES EN TANT QU'INHIBITEURS DE LA PHOSPHATIDYLINOSITOL 3-KINASE
    申请人:NOVARTIS AG
    公开号:WO2015162459A1
    公开(公告)日:2015-10-29
    The present invention provides compounds of formula (I) which inhibit the activity of PI 3-kinase gamma isoform, which are useful for the treatment of diseases mediated by the activation of PI 3-kinase gamma isoform.
    本发明提供了一种公式(I)的化合物,该化合物抑制PI 3-激酶γ同工酶的活性,对于治疗由PI 3-激酶γ同工酶激活介导的疾病是有用的。
  • [EN] NEW ARYL-QUINOLINE DERIVATIVES<br/>[FR] NOUVEAUX DÉRIVÉS D'ARYLQUINOLÉINE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2013064465A1
    公开(公告)日:2013-05-10
    The invention provides novel compounds having the general formula (I), wherein R1, R2, R3, R4 R5, R6 and n are as described herein, compositions including the compounds and methods of using the compounds.
    本发明提供了具有通用公式(I)的新颖化合物,其中R1、R2、R3、R4、R5、R6和n如本文所述,包括这些化合物的组合物以及使用这些化合物的方法。
  • NOVEL SUBSTITUTED TRIAZOLE DERIVATIVES AS GAMMA SECRETASE MODULATORS
    申请人:Van Brandt Sven Franciscus Anna
    公开号:US20120295891A1
    公开(公告)日:2012-11-22
    The present invention is concerned with novel substituted triazole derivatives of Formula (I) wherein Het 1 , R 1 , R 2 , A 1 , A 2 , A 3 , A 4 , L 1 , and L 2 have the meaning defined in the claims. The compounds according to the present invention are useful as gamma secretase modulators. The invention further relates to processes for preparing such novel compounds, pharmaceutical compositions comprising said compounds as an active ingredient as well as the use of said compounds as a medicament.
    本发明涉及具有以下式(I)的新型取代三唑衍生物,其中Het1,R1,R2,A1,A2,A3,A4,L1和L2的含义如权利要求中所定义。根据本发明的化合物可用作γ-分泌酶调节剂。本发明还涉及制备这种新型化合物的方法,包括将所述化合物作为活性成分的药物组合物以及将所述化合物用作药物的用途。
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