摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

环戊烷乙胺盐酸盐 | 684221-26-9

中文名称
环戊烷乙胺盐酸盐
中文别名
——
英文名称
2-cyclopentylethan-1-amine hydrochloride
英文别名
2-cyclopentyl-ethylamine; hydrochloride;2-Cyclopentyl-aethylamin; Hydrochlorid;2-(cyclopentyl)ethylamine HCl salt;2-Cyclopentylethanamine hydrochloride;2-cyclopentylethanamine;hydrochloride
环戊烷乙胺盐酸盐化学式
CAS
684221-26-9
化学式
C7H15N*ClH
mdl
MFCD09866300
分子量
149.664
InChiKey
PSWQBGNJVWDEOE-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:
    197℃

计算性质

  • 辛醇/水分配系数(LogP):
    1.41
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    26
  • 氢给体数:
    2
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2921300090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

SDS

SDS:75e4b8a5a901741ac398205bf9b29567
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2-Cyclopentylethanamine HCl
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 2-Cyclopentylethanamine HCl
CAS number: 684221-26-9

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: C7H16ClN
Molecular weight: 149.7

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.

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:
    3-溴苯甲酰氯环戊烷乙胺盐酸盐 在 sodium hydroxide 作用下, 以 二氯甲烷 为溶剂, 反应 18.0h, 以99%的产率得到3-bromo-N-(2-cyclopentylethyl)benzamide
    参考文献:
    名称:
    WO2020011811A5
    摘要:
    公开号:
    WO2020011811A5
  • 作为产物:
    描述:
    (2-azidoethyl)cyclopentane 在 palladium 10% on activated carbon 氢气盐酸 作用下, 以 甲醇乙醚 为溶剂, 反应 17.0h, 以51%的产率得到环戊烷乙胺盐酸盐
    参考文献:
    名称:
    [EN] IMIDAZOLYL PYRIMIDINE DERIVATIVES USEFUL AS IL-8 RECEPTOR MODULATORS
    [FR] DERIVES DE D'IMIDAZOLYL PYRIMIDINE UTILISES COMME MODULATEURS DU RECEPTEUR DE IL-8
    摘要:
    该发明涉及公式I的化合物,其中R1、R2、R3和R4分别独立地选择自H、(1-4C)烷基、(1-4C)烷氧基、三氟甲基、三氟甲氧基、卤素、氨基、磺酰胺基、氰基、羟基和硝基;R5为H或(1-6C)烷基;R6为H、(1-6C)烷基或(1-6C)烷氧基;R7为H或(1-6C)烷基;R8为(1-6C)烷基,可选地取代为(1-6C)烷氧基;R9为-(CH2)nR10,其中n为1、2或3,R10选自(1-4C)烷氧基、(1-4C)烷基硫醚、三氟甲基、(3-8C)环烷基、苯基,可选地取代为(1-4C)烷氧基,-NR11R12和-O(CH2)2NR11R12,其中R11和R12中的一个为(1-4C)烷氧基,另一个为H或(1-4C)烷基,或R9为-CH2(2-7C)杂环烷基,但至少一个杂原子在杂环烷基基团中是氮时,该氮与“NHR9”中的氮之间的距离至少为三个碳原子,或R9为-(CH2)3(2-7C)杂环烷基或-(CH2)2CHR13R14,其中R13和R14与它们连接的碳原子一起,是(2-7C)杂环烷基;X为O、S或NH;或其药学上可接受的盐。该发明的化合物是Il-8受体调节剂,特别是其抑制剂,并可用于治疗或预防Il-8受体介导的疾病,如动脉粥样硬化、炎症、类风湿关节炎及相关疾病。
    公开号:
    WO2004063192A1
点击查看最新优质反应信息

文献信息

  • Pyrimidine derivatives as IL-8 receptor antagonists
    申请人:——
    公开号:US20040087601A1
    公开(公告)日:2004-05-06
    Compounds containing the pyrimidine nucleus and their use to treat diseases and conditions related to inappropriate Interleukin-8 receptor activity are disclosed. The compounds are of the formula I 1 In these compounds, Q is preferably unsubstituted and substituted heterocyclyl; U is usually hydrogen or fluorine; and V is preferably hydrogen, halogen, alkyl, —O—alkyl or —S-alkyl. A representative example is: 2
    含有嘧啶核的化合物及其用于治疗与不适当的白细胞介素-8受体活性相关的疾病和症状的用途已被披露。这些化合物的结构式为I 1 在这些化合物中,Q最好是未取代或取代的杂环烷基;U通常是氢或氟;V最好是氢、卤素、烷基、—O—烷基或—S-烷基。一个代表性的例子是: 2
  • NOVEL INDOLE DERIVATIVES AND THEIR USE IN NEURODEGENERATIVE DISEASES
    申请人:Merck Patent GmbH
    公开号:US20160168090A1
    公开(公告)日:2016-06-16
    The present invention relates to indole compounds, and pharmaceutically acceptable compositions thereof, useful as antagonists of P2X7, and for the treatment of P2X7-related disorders.
    本发明涉及吲哚化合物及其药用可接受的组合物,用作P2X7拮抗剂,用于治疗与P2X7相关的疾病。
  • [EN] BICYCLIC JAK INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS DE JAK BICYCLIQUES ET LEURS UTILISATIONS
    申请人:INSILICO MEDICINE IP LTD
    公开号:WO2020198583A1
    公开(公告)日:2020-10-01
    Provided herein are compounds of Formulas (I), (II), (III), and (IV) and subformulas thereof, wherein the variables are defined herein. Also provided herein are pharmaceutical compositions comprising a compound of Formula (I), (II), (III), or (IV) and methods of using the compounds, e.g., in the treatment of immune disorders, inflammatory disorders, and cancer.
    本文提供了公式(I)、(II)、(III)和(IV)及其子公式的化合物,其中变量在此处定义。本文还提供了包括公式(I)、(II)、(III)或(IV)化合物的药物组合物,以及使用这些化合物的方法,例如用于治疗免疫紊乱、炎症性疾病和癌症。
  • [EN] DISUBSTITUTED HETEROARYL-FUSED PYRIDINES<br/>[FR] PYRIDINES ACCOLÉES À DI-SUBSTITUTION HÉTÉROARYLE
    申请人:NOVARTIS AG
    公开号:WO2011076744A1
    公开(公告)日:2011-06-30
    The invention relates to compound of the formula (I') in which the substituents are as defined in the specification; in free form or in salt form; to its preparation, to its use as medicament and to medicaments comprising it.
    这项发明涉及公式(I')的化合物,其中取代基如规范中所定义;以自由形式或盐形式存在;其制备方法,其作为药物的用途以及包含它的药物。
  • DIHYDRO-PYRROLOPYRIDINONE INHIBITORS
    申请人:AbbVie Inc.
    公开号:US20160237084A1
    公开(公告)日:2016-08-18
    The present invention provides for compounds of formula (I) wherein R 1 , R 2 , R 3 , R 4 , and R 5 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions, including inflammatory diseases, cancer, and AIDS. Also provided are pharmaceutical compositions comprising one or more compounds of formula (I).
    本发明提供了式(I)的化合物,其中R1、R2、R3、R4和R5具有规范中定义的任何值,以及其药学上可接受的盐,它们在治疗疾病和病况方面是有用的,包括炎症性疾病、癌症和艾滋病。还提供了包含一种或多种式(I)化合物的制药组合物。
查看更多

同类化合物

(N-(2-甲基丙-2-烯-1-基)乙烷-1,2-二胺) (4-(苄氧基)-2-(哌啶-1-基)吡啶咪丁-5-基)硼酸 (11-巯基十一烷基)-,,-三甲基溴化铵 鼠立死 鹿花菌素 鲸蜡醇硫酸酯DEA盐 鲸蜡硬脂基二甲基氯化铵 鲸蜡基胺氢氟酸盐 鲸蜡基二甲胺盐酸盐 高苯丙氨醇 高箱鲀毒素 高氯酸5-(二甲氨基)-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-2-甲基吡啶正离子 高氯酸2-氯-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-6-甲基吡啶正离子 高氯酸2-(丙烯酰基氧基)-N,N,N-三甲基乙铵 马诺地尔 马来酸氢十八烷酯 马来酸噻吗洛尔EP杂质C 马来酸噻吗洛尔 马来酸倍他司汀 顺式环己烷-1,3-二胺盐酸盐 顺式氯化锆二乙腈 顺式吡咯烷-3,4-二醇盐酸盐 顺式双(3-甲氧基丙腈)二氯铂(II) 顺式3,4-二氟吡咯烷盐酸盐 顺式1-甲基环丙烷1,2-二腈 顺式-二氯-反式-二乙酸-氨-环己胺合铂 顺式-二抗坏血酸(外消旋-1,2-二氨基环己烷)铂(II)水合物 顺式-N,2-二甲基环己胺 顺式-4-甲氧基-环己胺盐酸盐 顺式-4-环己烯-1.2-二胺 顺式-4-氨基-2,2,2-三氟乙酸环己酯 顺式-2-甲基环己胺 顺式-2-(苯基氨基)环己醇 顺式-2-(氨基甲基)-1-苯基环丙烷羧酸盐酸盐 顺式-1,3-二氨基环戊烷 顺式-1,2-环戊烷二胺 顺式-1,2-环丁腈 顺式-1,2-双氨甲基环己烷 顺式--N,N'-二甲基-1,2-环己二胺 顺式-(R,S)-1,2-二氨基环己烷铂硫酸盐 顺式-(2-氨基-环戊基)-甲醇 顺-2-戊烯腈 顺-1,3-环己烷二胺 顺-1,3-双(氨甲基)环己烷 顺,顺-丙二腈 非那唑啉 靛酚钠盐 靛酚 霜霉威盐酸盐 霜脲氰