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[4-(1-吡咯烷基)苯基]甲胺 | 114365-04-7

中文名称
[4-(1-吡咯烷基)苯基]甲胺
中文别名
4-(1-吡咯烷)苄胺;4-(1-吡咯烷基)苯基甲胺
英文名称
(4-(pyrrolidin-1-yl)phenyl)methanamine
英文别名
(4-pyrrolidin-1-ylphenyl)methanamine;4-(pyrrolidin-1-yl)-phenylmethylamine;4-(1-pyrrolidinyl)benzylamine;4-(1-pyrrolidino)benzylamine
[4-(1-吡咯烷基)苯基]甲胺化学式
CAS
114365-04-7
化学式
C11H16N2
mdl
——
分子量
176.261
InChiKey
OCVQUKOCFUOCBM-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:
    327.0±25.0 °C(Predicted)
  • 密度:
    1.075±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    29.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi,C
  • 海关编码:
    2933990090
  • 包装等级:
    III
  • 危险类别:
    8
  • 危险性防范说明:
    P280,P305+P351+P338,P310
  • 危险品运输编号:
    3259
  • 危险性描述:
    H314

SDS

SDS:3756fd48b69be7c033538bce57b693d6
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: [4-(1-Pyrrolidinyl)phenyl]methanamine
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

Section 3. Composition/information on ingredients.
Ingredient name: [4-(1-Pyrrolidinyl)phenyl]methanamine
CAS number: 114365-04-7

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, refrigerated.
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
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C11H16N2
Molecular weight: 176.3

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

  • 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:
    [4-(1-吡咯烷基)苯基]甲胺 生成 ethyl 5-(4-fluorophenyl)-2-(4-(1-pyrrolidinyl)phenyl)imidazole-4-carboxylate
    参考文献:
    名称:
    Imidazole derivatives
    摘要:
    本发明涉及以下式(I)的咪唑衍生物 其中R1是氢,可选择地取代的烷基等,R2是氢,可选择地取代的烷基等,R3是可选择地取代的杂芳基,R4是可选择地取代的环烷基,可选择地取代的苯基等,但当R1是氢,且R2和R4相同或不同,且每个是苯基或被卤原子、较低烷基或较低烷氧基取代的苯基时,R3是苯并噻唑基或被苯基取代的噻唑基,以下式(XII)的咪唑衍生物 其中R6是可选择地取代的苯基或可选择地取代的杂芳基,R7是被取代的苯基,以及其药学上可接受的盐。本发明的式(I)和(XII)的化合物及其药学上可接受的盐通过抑制Th2细胞产生IL-4和IL-5,在预防和治疗特应性皮炎、支气管哮喘、过敏性鼻炎等过敏性疾病方面具有有效性。
    公开号:
    US06288061B1
  • 作为产物:
    描述:
    4-(1-吡咯啉基)苯甲醛盐酸羟胺sodium acetate 、 lithium aluminium tetrahydride 作用下, 以 乙醇四氢呋喃 为溶剂, 反应 25.0h, 生成 [4-(1-吡咯烷基)苯基]甲胺
    参考文献:
    名称:
    NOVEL BRONCHODILATING DIAZAHETEROARYLS
    摘要:
    这项发明涉及具有通式(I)的新化合物,这些化合物可用于治疗由支气管痉挛引起的疾病或疾病,例如慢性阻塞性肺疾病(COPD)和哮喘。
    公开号:
    US20120040942A1
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文献信息

  • Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor
    申请人:——
    公开号:US20040157849A1
    公开(公告)日:2004-08-12
    Compounds of formula (I) 1 are novel VR1 antagonists that are useful in treating pain, inflammatory thermal hyperalgesia, urinary incontinence and bladder overactivity.
    式(I)的化合物是新颖的VR1拮抗剂,可用于治疗疼痛、炎症性热性过敏、尿失禁和膀胱过度活动。
  • Biphenylcarboxylic acid amides, the preparation thereof and the use thereof as medicaments
    申请人:——
    公开号:US20020032238A1
    公开(公告)日:2002-03-14
    The present invention relates to substituted piperazine derivatives of general formula 1 wherein R 1 to R 7 are defined herein, the isomers and salts thereof, particularly the physiologically acceptable salts thereof, which are valuable inhibitors of the microsomal triglyceride-transfer protein (MTP), medicaments containing these compounds and their use, as well as the preparation thereof.
    本发明涉及一般式1的取代哌嗪衍生物,其中R1至R7在此处定义,其异构体和盐,特别是其生理上可接受的盐,这些盐是微粒体三酰甘油转移蛋白(MTP)的有价值的抑制剂,含有这些化合物的药物以及它们的用途,以及其制备。
  • SUBSTITUTED PTERIDINES FOR THE TREATMENT AND PREVENTION OF VIRAL INFECTIONS
    申请人:Herdewijn Piet André Maurits Maria
    公开号:US20090318456A1
    公开(公告)日:2009-12-24
    Tri-substituted pteridines and tetra-substituted pteridines exhibit a significant and selective activity against certain types of viral infections, in particular they selectively inhibit the replication of the hepatitis C virus, and are useful for the prevention and treatment of such infections.
    三取代喹啉和四取代喹啉对某些类型的病毒感染表现出显著和选择性的活性,特别是它们选择性地抑制丙型肝炎病毒的复制,并可用于预防和治疗此类感染。
  • [EN] "TRPV1 VANILLOID RECEPTOR ANTAGONISTS WITH A BICYCLIC PORTION"<br/>[FR] ANTAGONISTES DU RÉCEPTEUR VANILLOÏDE TRPV1 AYANT UNE PARTIE BICYCLIQUE
    申请人:PHARMESTE SRL
    公开号:WO2011120604A1
    公开(公告)日:2011-10-06
    The invention discloses compounds of formula I wherein Y is a group of formula A, B, C, D, or E: and W, Q, n, R1, R2, R3, U1-U5, J and K have the meanings given in the description. The compounds of formula I are TRPV1 antagonists and are useful as active ingredients of pharmaceutical compositions for the treatment of pain and other conditions ameliorated by the inhibition of the vanilloid receptor TRPV1.
    该发明揭示了公式I的化合物,其中Y是公式A、B、C、D或E的一个基团;W、Q、n、R1、R2、R3、U1-U5、J和K具有描述中给出的含义。公式I的化合物是TRPV1拮抗剂,可用作药物组合物的活性成分,用于治疗通过抑制辣椒素受体TRPV1而改善的疼痛和其他病症。
  • TRPV1 vanilloid receptor antagonists with a bicyclic portion
    申请人:Pharmeste S.r.l.
    公开号:EP2377850A1
    公开(公告)日:2011-10-19
    The invention discloses compounds of formula I wherein Y s selected from a group of formula and W, Q, n, R1, R2, R3, U1-U5 have the meanings given in the description. The compounds of formula I are TRPV1 antagonists and are useful as active ingredients of pharmaceutical compositions for the treatment of pain and other conditions ameliorated by the inhibition of the vanilloid receptor TRPV1. 1.
    该发明揭示了以下式的化合物: 其中Y选自以下式的一组 而W、Q、n、R1、R2、R3、U1-U5的含义如描述中所给出。 该式化合物是TRPV1拮抗剂,可用作药物组合物的活性成分,用于治疗疼痛和其他通过抑制辣椒素受体TRPV1而改善的症状。
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