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5-异丙基吡啶-2-胺 | 603310-75-4

中文名称
5-异丙基吡啶-2-胺
中文别名
5-(1-甲乙基)-2-氨基吡啶
英文名称
5-isopropylpyridin-2-amine
英文别名
2-amino-5-isopropylpyridine;5-propan-2-ylpyridin-2-amine
5-异丙基吡啶-2-胺化学式
CAS
603310-75-4
化学式
C8H12N2
mdl
——
分子量
136.197
InChiKey
GXSWKKZGLOYAPE-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:
    253 ºC
  • 密度:
    1.008
  • 闪点:
    130 ºC

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 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
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

SDS

SDS:83bd96d0a946252c9544040120cc5552
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 5-(1-Methylethyl)-2-pyridinamine
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 5-(1-Methylethyl)-2-pyridinamine
CAS number: 603310-75-4

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: C8H12N2
Molecular weight: 136.2

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

制备方法与用途

用途

5-异丙基吡啶-2-胺可用作医药合成中间体。

危险处理

如吸入5-异丙基吡啶-2-胺,请将患者移至空气新鲜处;如皮肤接触到,应脱去污染衣物,并用肥皂和清彻底清洗皮肤,如有不适,应及时就医;如眼睛接触,需分开眼睑,使用流动清或生理盐冲洗,并立即就医;如误食,应立即漱口,禁止催吐,并尽快就医。

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:
    5-异丙基吡啶-2-胺 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以50%的产率得到3-bromo-5-isopropylpyridin-2-amine
    参考文献:
    名称:
    [EN] COMPOUNDS AND METHODS FOR TREATMENT OF HEDGEHOG PATHWAY ASSOCIATED CONDITIONS
    [FR] COMPOSÉS ET MÉTHODES POUR LE TRAITEMENT D'AFFECTIONS ASSOCIÉES À LA VOIE HEDGEHOG
    摘要:
    本文提供了规范中描述的式(I)、(II)、(III)、(IV)和(V)的新化合物,以及其药学上可接受的盐、溶剂化合物、前药和组合物,以及测量肿瘤细胞中刺猬途径激活、检查肿瘤细胞增殖、分化和凋亡的方法,以及使用所披露的化合物和药物组合物治疗与刺猬信号通路相关的疾病和疾病的方法。
    公开号:
    WO2020003119A1
  • 作为产物:
    描述:
    3-溴-4-甲氧基吡啶四(三苯基膦)钯 、 palladium 10% on activated carbon 、 氢气potassium carbonate 作用下, 以 1,4-二氧六环甲醇 为溶剂, 20.0~100.0 ℃ 、400.01 kPa 条件下, 反应 36.0h, 生成 5-异丙基吡啶-2-胺
    参考文献:
    名称:
    EP3712144
    摘要:
    公开号:
点击查看最新优质反应信息

文献信息

  • [EN] OXADIAZOLE INHIBITORS OF LEUKOTRIENE PRODUCTION<br/>[FR] COMPOSÉS OXADIAZOLE, INHIBITEURS DE LA PRODUCTION DE LEUCOTRIÈNES
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2012027322A1
    公开(公告)日:2012-03-01
    The present invention relates to compound of formula (I) and pharmaceutically acceptable salt thereof, wherein R1-R5 are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.
    本发明涉及式(I)的化合物及其药用可接受盐,其中R1-R5如本文所定义。该发明还涉及包括这些化合物的药物组合物,使用这些化合物治疗各种疾病和疾病的方法,制备这些化合物的过程以及在这些过程中有用的中间体。
  • MASP-2 INHIBITORS AND METHODS OF USE
    申请人:Omeros Corporation
    公开号:US20210171512A1
    公开(公告)日:2021-06-10
    The present disclosure provides, inter alia, compounds with MASP-2 inhibitory activity, compositions of such compounds, and methods of making and using such compounds.
    本公开提供了具有MASP-2抑制活性的化合物,这些化合物的组合物,以及制造和使用这些化合物的方法。
  • BENZOPYRAN AND BENZOXEPIN PI3K INHIBITOR COMPOUNDS AND METHODS OF USE
    申请人:Do Steven
    公开号:US20090247567A1
    公开(公告)日:2009-10-01
    Benzopyran and benzoxepin compounds of Formulas I and II, and including stereoisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting lipid kinases including p110 alpha and other isoforms of PI3K, and for treating disorders such as cancer mediated by lipid kinases. Methods of using compounds of Formulas I and II for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
    Benzopyran和benzoxePIn的化合物I和II的分子式,包括其立体异构体、几何异构体、互变异构体、溶剂合物、代谢物和药学上可接受的盐,可用于抑制脂质激酶,包括p110 alpha和PI3K的其他同系物,并用于治疗由脂质激酶介导的癌症等疾病。公开了使用分子式I和II的化合物在哺乳动物细胞中进行体外、体内和体内诊断、预防或治疗此类疾病或相关病理条件的方法。
  • BENZOXEPIN PI3K INHIBITOR COMPOUNDS AND METHODS OF USE
    申请人:Blaquiere Nicole
    公开号:US20110076291A1
    公开(公告)日:2011-03-31
    Benzoxepin compounds of Formula I, and including stereoisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, wherein: Z 1 is CR 1 or N; Z 2 is CR 2 or N; Z 3 is CR 3 or N; Z 4 is CR 4 or N; and where (i) X 1 is N and X 2 is S, (ii) X 1 is S and X 2 is N, (iii) X 1 is CR 7 and X 2 is S, (iv) X 1 is S and X 2 is CR 7 ; (v) X 1 is NR 8 and X 2 is N, (vi) X 1 is N and X 2 is NR 8 , (vii) X 1 is CR 7 and X 2 is O, (viii) X 1 is O and X 2 is CR 7 , (ix) X 1 is CR 7 and X 2 is C(R 7 ) 2 , (x) X 1 is C(R 7 ) 2 and X 2 is CR 7 ; (xi) X 1 is N and X 2 is O, or (xii) X 1 is O and X 2 is N, are useful for inhibiting lipid kinases including p110 alpha and other isoforms of PI3K, and for treating disorders such as cancer mediated by lipid kinases. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
    Formula I中的苯并氧杂环化合物,包括立体异构体、几何异构体、互变异构体、溶剂化合物、代谢物和其药学上可接受的盐,其中:Z1为CR1或N;Z2为CR2或N;Z3为CR3或N;Z4为CR4或N;其中(i)X1为N且X2为S,(ii)X1为S且X2为N,(iii)X1为CR7且X2为S,(iv)X1为S且X2为CR7;(v)X1为NR8且X2为N,(vi)X1为N且X2为NR8,(vii)X1为CR7且X2为O,(viii)X1为O且X2为CR7,(ix)X1为CR7且X2为C(R7)2,(x)X1为C(R7)2且X2为CR7;(xi)X1为N且X2为O,或(xii)X1为O且X2为N,用于抑制脂质激酶,包括p110α和PI3K的其他同工酶,并用于治疗由脂质激酶介导的癌症等疾病。公开了利用Formula I中的化合物在哺乳动物细胞中进行体外、体内和体内诊断、预防或治疗此类疾病或相关病理状况的方法。
  • HETEROCYCLIC COMPOUNDS AS PI3K-y INHIBITORS
    申请人:Incyte Corporation
    公开号:US20180009816A1
    公开(公告)日:2018-01-11
    This application relates to compounds of Formula (I): or pharmaceutically acceptable salts or stereoisomers thereof, which are inhibitors of PI3K-γ which are useful for the treatment of disorders such as autoimmune diseases, cancer, cardiovascular diseases, and neurodegenerative diseases.
    这种应用涉及到式(I)的化合物: 或其药用可接受的盐或立体异构体,这些化合物是PI3K-γ的抑制剂,对于治疗自身免疫疾病、癌症、心血管疾病和神经退行性疾病等疾病是有用的。
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