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N-甲基-N-2,2,2-三氟甲基乙胺盐酸盐 | 2730-52-1

中文名称
N-甲基-N-2,2,2-三氟甲基乙胺盐酸盐
中文别名
N-甲基-2,2,2-三氟乙胺盐酸盐
英文名称
2,2,2-trifluoro-N-methylethanamine hydrochloride
英文别名
methyl (2,2,2-trifluoroethyl)amine hydrochloride;2,2,2-trifluoro-N-methylethan-1-amine hydrochloride;N-methyl-N-(2,2,2-trifluoroethyl)amine hydrochloride;Methyl(2,2,2-trifluoroethyl)azanium;chloride;methyl(2,2,2-trifluoroethyl)azanium;chloride
N-甲基-N-2,2,2-三氟甲基乙胺盐酸盐化学式
CAS
2730-52-1
化学式
C3H6F3N*ClH
mdl
MFCD08448126
分子量
149.543
InChiKey
CUOWKFXFKFXJEL-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:
    >200 °C (sublm)(Solv: ethanol (64-17-5))

计算性质

  • 辛醇/水分配系数(LogP):
    0.76
  • 重原子数:
    8
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    12
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2921199090
  • 危险性防范说明:
    P305+P351+P338
  • 危险性描述:
    H302,H319

SDS

SDS:d56222292c67d3c9b29d673b79a4f947
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2,2,2-Trifluoro-N-methylethanamine HCl
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H302: Harmful if swallowed
H319: Causes serious eye irritation
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: 2,2,2-Trifluoro-N-methylethanamine HCl
CAS number: 2730-52-1

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.
Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
Eye contact:
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.
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
Appearance: Not specified
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C3H7ClF3N
Molecular weight: 149.5

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 chloride, hydrogen fluoride.

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:
    参考文献:
    名称:
    Fluorine-Containing Nitrogen Compounds. I. Trifluoroethylamines
    摘要:
    DOI:
    10.1021/jo01091a024
  • 作为产物:
    描述:
    N-甲基-2,2,2-三氟乙酰胺 在 lithium aluminium tetrahydride 、 Glauber's salt盐酸 作用下, 以 乙醚 为溶剂, 以80.7%的产率得到N-甲基-N-2,2,2-三氟甲基乙胺盐酸盐
    参考文献:
    名称:
    [EN] CYCLOBUTENEDIONE DERIVATIVES
    [FR] DÉRIVÉS DE CYCLOBUTÈNE-DIONE
    摘要:
    本发明涉及以下式(I)的化合物:以及其药学上可接受的盐和所述化合物及盐的药学上可接受的溶剂化物,其中取代基在此处定义;含有这种化合物的组合物;以及这种化合物在治疗各种疾病,特别是炎症性疾病中的用途。
    公开号:
    WO2010131145A1
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文献信息

  • POSITIVE ALLOSTERIC MODULATORS OF MUSCARINIC M2 RECEPTOR
    申请人:Bayer Pharma Aktiengesellschaft
    公开号:US20180297994A1
    公开(公告)日:2018-10-18
    The present application relates to positive allosteric modulators of the muscarinic M2 receptor, especially to novel 7-substituted 1-arylnaphthyridine-3-carboxamides, to processes for preparation thereof, to the use thereof, alone or in combinations, for treatment and/or prevention of diseases, and to the use thereof for production of medicaments for treatment and/or prevention of diseases, in particular for treatment and/or prevention of cardiovascular disorders and/or renal disorders.
    本申请涉及肌动蛋白M2受体的阳性变构调节剂,特别是新型的7-取代的1-芳基萘啶-3-羧酰胺,以及其制备方法,单独或组合使用于治疗和/或预防疾病,以及用于生产治疗和/或预防疾病的药物,特别是用于治疗和/或预防心血管疾病和/或肾脏疾病。
  • [EN] 2-METHYL-QUINAZOLINES<br/>[FR] 2-MÉTHYL-QUINAZOLINES
    申请人:BAYER PHARMA AG
    公开号:WO2018172250A1
    公开(公告)日:2018-09-27
    The present invention describes 2-methyl-quinazoline compounds of general formula (I), methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions. The 2-methyl substituted quinazoline compounds of general formula(I) effectively and selectively inhibit the Ras-Sos interaction without significantly targeting the EGFR receptor. They are therefore useful for the treatment or prophylaxis of diseases, in particular of hyperproliferative disorders, such as cancer as a sole agent or in combination with other active ingredients.
    本发明描述了一般式(I)的2-甲基喹唑啉化合物,制备该化合物的方法,用于制备该化合物的中间体化合物,包含该化合物的药物组合物和组合物,以及用于制造药物组合物的该化合物的用途。一般式(I)的2-甲基取代喹唑啉化合物有效且选择性地抑制Ras-Sos相互作用,而不显著靶向EGFR受体。因此,它们对于治疗或预防疾病特别是高增殖性疾病,如癌症作为单一药剂或与其他活性成分组合使用是有用的。
  • [EN] OXADIAZEPINONE DERIVATIVES AND THEIR USE IN THE TREATMENT OF HEPATITIS B INFECTIONS<br/>[FR] DÉRIVÉS D'OXADIAZÉPINONE ET LEUR UTILISATION DANS LE TRAITEMENT D'INFECTIONS PAR L'HÉPATITE B
    申请人:NOVIRA THERAPEUTICS INC
    公开号:WO2018005881A1
    公开(公告)日:2018-01-04
    Provided herein are compounds of formula (IA) and (III) useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.
    本文提供了公式(IA)和(III)的化合物,用于治疗需要治疗HBV感染的受试者,以及其药物组合物和抑制、抑制或预防受试者HBV感染的方法。
  • EIF4A-INHIBITING COMPOUNDS AND METHODS RELATED THERETO
    申请人:eFFECTOR Therapeutics, Inc.
    公开号:US20170145026A1
    公开(公告)日:2017-05-25
    The present invention provides synthesis, pharmaceutically acceptable formulations and uses of compounds in accordance with Formula I, or a stereoisomer, tautomer or pharmaceutically acceptable salt thereof. For Formula I compounds X, Y, R 1 , R 2 , R 3a , R 3b , R 4a , R 4b and R 5 are as defined in the specification. The inventive Formula I compounds are inhibitors of eIF4A and find utility in any number of therapeutic applications, including but not limited to treatment of inflammation and various cancers.
    本发明提供了根据式I合成的化合物、药用可接受的配方和用途,或其立体异构体、互变异构体或药用可接受的盐。对于式I化合物X、Y、R1、R2、R3a、R3b、R4a、R4b和R5如规范中所定义。这些创新的式I化合物是eIF4A的抑制剂,在许多治疗应用中发挥作用,包括但不限于治疗炎症和各种癌症。
  • [EN] PESTICIDALLY-ACTIVE CYANAMIDE HETEROCYCLIC COMPOUNDS<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES DE CYANAMIDE À ACTION PESTICIDE
    申请人:SYNGENTA CROP PROTECTION AG
    公开号:WO2020120697A1
    公开(公告)日:2020-06-18
    A compound of formula (I) wherein the substituents are as defined in claim 1, and the agrochemically acceptable salts, stereoisomers, enantiomers, tautomers and N-oxides of those compounds, can be used as insecticides.
    式(I)的化合物,其中取代基如权利要求1所定义,以及这些化合物的农化可接受盐、立体异构体、对映异构体、互变异构体和N-氧化物,可用作杀虫剂。
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