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1-(2-吡啶基)-3-甲基-1-丁胺 | 825647-69-6

中文名称
1-(2-吡啶基)-3-甲基-1-丁胺
中文别名
——
英文名称
3-methyl-1-(pyridin-2-yl)butan-1-amine
英文别名
3-methyl-1-pyridin-2-yl-butylamine;3-methyl-1-pyridin-2-ylbutan-1-amine
1-(2-吡啶基)-3-甲基-1-丁胺化学式
CAS
825647-69-6
化学式
C10H16N2
mdl
MFCD12153903
分子量
164.25
InChiKey
CQQSJHCEEUYAOK-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:
    245.4±15.0 °C(Predicted)
  • 密度:
    0.967±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    38.9
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933399090
  • 储存条件:
    室温且干燥

SDS

SDS:666d9ccc1880469d24bd8aa7ce79ccda
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 3-Methyl-1-(pyridin-2-yl)butan-1-amine
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 3-Methyl-1-(pyridin-2-yl)butan-1-amine
CAS number: 825647-69-6

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.
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: C10H16N2
Molecular weight: 164.3

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

  • 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:
    1-(2-吡啶基)-3-甲基-1-丁胺甲醇 、 sodium hydroxide 作用下, 以 甲醇 为溶剂, 反应 0.08h, 生成 (S)-3-methyl-1-(pyridin-2-yl)butan-1-amine
    参考文献:
    名称:
    [EN] KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME
    [FR] INHIBITEURS DE KINASE ET MÉTHODE DE TRAITEMENT DU CANCER À L'AIDE DE CEUX-CI
    摘要:
    该发明是由结构式(I)表示的化合物或其药学上可接受的盐。这里提供了变量的值。还包括一种含有由结构式(I)表示的化合物和药学上可接受的载体或稀释剂的药物组合物,以及使用结构式(I)的化合物治疗癌症患者的方法。
    公开号:
    WO2014056083A1
  • 作为产物:
    描述:
    2-(3-甲基丁基)吡啶 在 ammonium acetate 、 sodium cyanoborohydride 作用下, 以 甲醇 为溶剂, 反应 3.0h, 以25%的产率得到1-(2-吡啶基)-3-甲基-1-丁胺
    参考文献:
    名称:
    [EN] 2, 4, 6-TRI-SUBSTITUTED 6-MEMBERED HETEROCYCLES AND THEIR USE IN THE TREATMENT OF NEURODEGENERATIVE DISEASES
    [FR] NOUVEAUX HETEROCYCLES 2,4,6-TRISUBSTITUES ET UTILISATIONS DE CEUX-CI
    摘要:
    公开号:
    WO2005003103A3
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文献信息

  • [EN] PYRIDIN- 2 -AMIDES USEFUL AS CB2 AGONISTS<br/>[FR] PYRIDIN-2-AMIDES UTILES COMME AGONISTES DE CB2
    申请人:HOFFMANN LA ROCHE
    公开号:WO2012168350A1
    公开(公告)日:2012-12-13
    The invention relates to a compound of formula (I) wherein R1 to R4 are defined as in the description and in the claims. The compound of formula (I) can be used as a medicament.
    本发明涉及式(I)的化合物,其中R1至R4的定义如描述和权利要求中所述。式(I)的化合物可以用作药物。
  • NOVEL PYRIDINE DERIVATIVES
    申请人:Bissantz Caterina
    公开号:US20120316147A1
    公开(公告)日:2012-12-13
    The invention relates to a compound of formula (I) wherein R 1 to R 4 are defined as in the description and in the claims. The compound of formula (I) can be used as a medicament.
    本发明涉及一种公式(I)的化合物 其中R1至R4定义如描述和权利要求中所述。公式(I)的化合物可作为药物使用。
  • KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME
    申请人:Pauls Heinz W.
    公开号:US20140005167A1
    公开(公告)日:2014-01-02
    The present teachings provide a compound represented by structural formula (I): or a pharmaceutically acceptable salt thereof. Also described are pharmaceutical compositions and methods of use thereof.
    本教学提供了一种由结构式(I)表示的化合物,或其药用可接受的盐。还描述了药物组合物及其使用方法。
  • [EN] INDAZOLE COMPOUNDS AS KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME<br/>[FR] COMPOSÉS INDAZOLE UTILISÉS COMME INHIBITEURS DE KINASE ET MÉTHODE DE TRAITEMENT DU CANCER AVEC LESDITS COMPOSÉS
    申请人:UNIV HEALTH NETWORK
    公开号:WO2013053051A1
    公开(公告)日:2013-04-18
    The present teaching provide indazole compounds represented by Structural Formulae (I) or (I') or a pharmaceutically acceptable salt thereof. Also described are pharmaceutical compositions and methods of use thereof as protein kinase inhibitors, such as TTK protein kinase, polo-like kinase 4 (PLK4) and Aurora kinases having anticancer activity against breast cancer cells, colon cancer cells, and ovarian cancer cells.
    本教学提供了由结构式(I)或(I')表示的吲唑化合物或其药用可接受的盐。还描述了这些药物组合物及其用作蛋白激酶抑制剂的方法,如对乳腺癌细胞、结肠癌细胞和卵巢癌细胞具有抗癌活性的TTK蛋白激酶、极化样激酶4(PLK4)和极化激酶。
  • INDAZOLE COMPOUNDS AS KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME
    申请人:University Health Network
    公开号:US20140371202A1
    公开(公告)日:2014-12-18
    The present teaching provide indazole compounds represented by Structural Formulae (I) or (I′) or a pharmaceutically acceptable salt thereof. Also described are pharmaceutical compositions and methods of use thereof as protein kinase inhibitors, such as TTK protein kinase, polo-like kinase 4 (PLK4) and Aurora kinases having anticancer activity against breast cancer cells, colon cancer cells, and ovarian cancer cells.
    本教学提供由结构式(I)或(I')所代表的吲唑化合物或其药学上可接受的盐。还描述了制备药物组合物和使用方法,作为蛋白激酶抑制剂,例如TTK蛋白激酶,极化样激酶4(PLK4)和极化激酶,对乳腺癌细胞,结肠癌细胞和卵巢癌细胞具有抗癌活性。
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