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N-环丙基-3-硼苯磺酰胺 | 913835-28-6

中文名称
N-环丙基-3-硼苯磺酰胺
中文别名
(3-(N-环丙基氨磺酰)苯基)硼酸;3-(环丙基氨磺酰基)苯硼酸
英文名称
(3-(N-cyclopropylsulfamoyl)phenyl)boronic acid
英文别名
[3-(cyclopropylsulfamoyl)phenyl]boronic acid
N-环丙基-3-硼苯磺酰胺化学式
CAS
913835-28-6
化学式
C9H12BNO4S
mdl
MFCD08436035
分子量
241.076
InChiKey
WIZSPBQIRRAOMO-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:
    126-128

计算性质

  • 辛醇/水分配系数(LogP):
    0.92
  • 重原子数:
    16
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    95
  • 氢给体数:
    3
  • 氢受体数:
    5

安全信息

  • 危险品标志:
    Xi
  • 海关编码:
    2935009090
  • 危险性防范说明:
    P261,P264,P271,P280,P304+P340,P302+P352,P305+P351+P338,P312,P362,P403+P233,P501
  • 危险性描述:
    H315,H319,H335

SDS

SDS:5dcc894d8f59ac5926d18dbee39bb75b
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Material Safety Data Sheet

Section 1. Identification of the substance
N-Cyclopropyl 3-boronobenzenesulfonamide
Product Name:
Synonyms: 3-(N-Cyclopropylsulfamoyl)phenylboronic acid

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.
N-Cyclopropyl 3-boronobenzenesulfonamide
Ingredient name:
CAS number: 913835-28-6

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.
Storage: Store in closed vessels.

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: C9H12BNO4S
Molecular weight: 241.1

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, sulfur 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

反应信息

  • 作为反应物:
    描述:
    6-氯-5-甲基-2-吡啶胺N-环丙基-3-硼苯磺酰胺(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloridepotassium carbonate 作用下, 以 乙二醇二甲醚 为溶剂, 以53%的产率得到3-(6-amino-3-methylpyridin-2-yl)-N-cyclopropylbenzene-1-sulfonamide
    参考文献:
    名称:
    SUBSTITUTED TRICYCLICS AND METHOD OF USE
    摘要:
    本发明提供了一种具有以下结构的化合物(I),其中X、Y和R1具有规范中定义的任何值,以及其药学上可接受的盐,这些化合物在治疗由CFTR介导和调节的疾病和症状中是有用的,包括囊性纤维化、Sjögren综合征、胰腺功能不全、慢性阻塞性肺病和慢性阻塞性气道疾病。还提供了由一个或多个具有结构(I)的化合物组成的药物组合物。
    公开号:
    US20170015675A1
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文献信息

  • Modular Synthesis of Di- and Trisubstituted Imidazoles from Ketones and Aldehydes: A Route to Kinase Inhibitors
    作者:Ian de Toledo、Thiago A. Grigolo、James M. Bennett、Jonathan M. Elkins、Ronaldo A. Pilli
    DOI:10.1021/acs.joc.9b01844
    日期:2019.11.1
    A one-pot and modular approach to the synthesis of 2,4(5)-disubstituted imidazoles was developed based on ketone oxidation, employing catalytic HBr and DMSO, followed by imidazole condensation with aldehydes. This methodology afforded twenty-nine disubstituted NH-imidazoles (23%-85% yield). A three-step synthesis of 20 kinase inhibitors was achieved by employing this oxidation-condensation protocol
    基于酮氧化,采用催化HBr和DMSO,然后通过咪唑与醛的缩合反应,开发了一种单罐模块化方法,用于合成2,4(5)-二取代的咪唑。该方法提供了二十九个二取代的NH-咪唑(23%-85%的产率)。通过采用这种氧化-缩合方案,然后在咪唑环中进行溴化和Suzuki偶联,得到三取代的NH-咪唑(23%-69%,三步法),实现了三步合成20种激酶抑制剂的过程。该方法还用于合成已知抑制剂GSK3037619A。
  • COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR
    申请人:Plexxikon Inc.
    公开号:US20170158690A1
    公开(公告)日:2017-06-08
    Disclosed are compounds of Formula I: or a pharmaceutically acceptable salt, a solvate, a tautomer, an isomer or a deuterated analog thereof, wherein Z 2 , Z 3 , and Z 5 are as described herein, compositions thereof, and uses thereof.
    公开了以下Formula I的化合物:或其药用可接受的盐、溶剂合物、互变异构体、同分异构体或其氘代物,其中Z2、Z3和Z5如本文所述,以及其组合物和用途。
  • Organic compounds
    申请人:BRUCE Ian
    公开号:US20090239847A1
    公开(公告)日:2009-09-24
    The present invention concerns a compound of formula (I) or a salt, suitably a pharmaceutically acceptable salt, or solvate thereof, wherein the groups R 1 , R 2 , Ar′, A and Y are defined in the description, to compositions and use of the compounds in the treatment of inflammatory and allergic conditions.
    本发明涉及一种化合物,其化学式为(I)或其盐,适宜为药用可接受的盐,或其溶剂化合物,其中基团R1、R2、Ar′、A和Y在描述中有定义,以及该化合物在治疗炎症和过敏症状中的应用。
  • SUBSTITUTED PHENYLALANINE DERIVATIVES
    申请人:BAYER PHARMA AKTIENGESELLSCHAFT
    公开号:US20160244437A1
    公开(公告)日:2016-08-25
    The invention relates to substituted phenylalanine derivatives and to processes for preparation thereof, and to the use thereof for production of medicaments for the treatment and/or prophylaxis of diseases, especially of cardiovascular disorders and/or severe perioperative blood loss.
    本发明涉及取代苯丙氨酸衍生物及其制备方法,以及将其用于生产用于治疗和/或预防疾病的药物,特别是心血管疾病和/或严重围手术期失血的药物。
  • KINASE INHIBITORS
    申请人:Brown Jason W.
    公开号:US20100120717A1
    公开(公告)日:2010-05-13
    Compounds are provided for use with kinases that comprise a compound selected from the group consisting of formula (I) wherein the variables are as defined herein. Also provided are pharmaceutical compositions, kits and articles of manufacture in comprising such compounds; methods and intermediates useful for making the compounds; and methods of using said compounds.
    提供化合物用于与包括从以下公式(I)中选择的化合物的激酶一起使用,其中变量如本文所定义。还提供了包含这些化合物的制药组合物、工具包和制造物品;有用于制造这些化合物的方法和中间体;以及使用这些化合物的方法。
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