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4-(N-苄氧羰基)-氨基哌啶 | 182223-54-7

中文名称
4-(N-苄氧羰基)-氨基哌啶
中文别名
4-Cbz-氨基哌啶;4-CBZ-氨基哌啶;4-(Cbz-氨基)哌啶
英文名称
benzyl piperidin-4-ylcarbamate
英文别名
benzyl N-(4-piperidyl)carbamate;benzyl N-(piperidin-4-yl)carbamate;4-benzyloxycarbonylamino-piperidine;4-Cbz-aminopiperidine;benzyl N-piperidin-4-ylcarbamate
4-(N-苄氧羰基)-氨基哌啶化学式
CAS
182223-54-7
化学式
C13H18N2O2
mdl
——
分子量
234.298
InChiKey
WWGUAFRTAYMNHU-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:
    396.3±41.0 °C(Predicted)
  • 密度:
    1.13±0.1 g/cm3(Predicted)
  • 溶解度:
    溶于二氯甲烷

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    50.4
  • 氢给体数:
    2
  • 氢受体数:
    3

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
  • 储存条件:
    室温

SDS

SDS:768bfb0975e667378be3ff6ad7a7d7ea
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: Benzyl N-(piperidin-4-yl)carbamate
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: Benzyl N-(piperidin-4-yl)carbamate
CAS number: 182223-54-7

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: C13H18N2O2
Molecular weight: 234.3

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

制备方法与用途

4-(N-苄氧羰基)-氨基哌啶是一种哌啶类衍生物,具有广泛的应用价值,主要应用于医药合成领域。

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-(N-苄氧羰基)-氨基哌啶 在 palladium 10% on activated carbon 、 氢气三乙酰氧基硼氢化钠N,N-二异丙基乙胺 作用下, 以 2,2,2-三氟乙醇 为溶剂, 反应 5.5h, 生成 1-环戊基-4-氨基哌啶
    参考文献:
    名称:
    2,4-二取代喹唑啉类化合物、及其制法和药物 组合物与用途
    摘要:
    本发明公开了一类新的2,4‑二取代喹唑啉类化合物、及其制法和药物组合物与用途。具体而言,涉及通式I所示的2,4‑二取代喹唑啉类化合物,其可药用盐,其同样生物功能的前体或衍生物,及其制备方法,含有一个或多个这化合物的组合物,和该类化合物在对Pin1酶的抑制活性和对肿瘤生长的抑制活性等方面的用途。
    公开号:
    CN102250075B
  • 作为产物:
    描述:
    氯甲酸苄酯N,N-二异丙基乙胺三氟乙酸 作用下, 以 二氯甲烷氯仿 为溶剂, 反应 13.0h, 生成 4-(N-苄氧羰基)-氨基哌啶
    参考文献:
    名称:
    2,4-二取代喹唑啉类化合物、及其制法和药物 组合物与用途
    摘要:
    本发明公开了一类新的2,4‑二取代喹唑啉类化合物、及其制法和药物组合物与用途。具体而言,涉及通式I所示的2,4‑二取代喹唑啉类化合物,其可药用盐,其同样生物功能的前体或衍生物,及其制备方法,含有一个或多个这化合物的组合物,和该类化合物在对Pin1酶的抑制活性和对肿瘤生长的抑制活性等方面的用途。
    公开号:
    CN102250075B
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文献信息

  • [EN] 1,3 DI-SUBSTITUTED CYCLOBUTANE OR AZETIDINE DERIVATIVES AS HEMATOPOIETIC PROSTAGLANDIN D SYNTHASE INHIBITORS<br/>[FR] DÉRIVÉS D'AZÉTIDINE OU DE CYCLOBUTANE 1,3-DISUBSTITUÉS UTILISÉS COMME INHIBITEURS DE LA PROSTAGLANDINE D SYNTHASE HÉMATOPOÏÉTIQUE (H-PGDS)
    申请人:GLAXOSMITHKLINE IP DEV LTD
    公开号:WO2018069863A1
    公开(公告)日:2018-04-19
    A compound of formula (I), wherein R, R1, R2, R3, Y, Y1, a, X, and Z are as defined herein. The compounds of the present invention are inhibitors of hematopoietic prostaglandin D synthase (H-PGDS) and can be useful in the treatment of Duchenne Muscular Dystrophy. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting H-PGDS activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.
    式(I)的化合物,其中R、R1、R2、R3、Y、Y1、a、X和Z的定义如本文所述。本发明的化合物是造血前列腺素D合成酶(H-PGDS)的抑制剂,可用于治疗杜兴氏肌肉萎缩症。因此,本发明进一步涉及包含本发明化合物的药物组合物。本发明还进一步涉及使用本发明化合物或包含本发明化合物的药物组合物来抑制H-PGDS活性和治疗相关疾病的方法。
  • [EN] 3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS DE LA 3-PHOSPHOGLYCÉRATE DÉSHYDROGÉNASE) ET LEURS UTILISATIONS
    申请人:RAZE THERAPEUTICS INC
    公开号:WO2016040449A1
    公开(公告)日:2016-03-17
    The present invention provides compounds, compositions and methods useful for treating a variety of diseases, disorders or conditions, associated with PHGDH.
    本发明提供了一种用于治疗与PHGDH相关的各种疾病、疾病或病况的化合物、组合物和方法。
  • OXAZOLIDINONE ANTIBIOTICS
    申请人:Bur Daniel
    公开号:US20110039823A1
    公开(公告)日:2011-02-17
    The invention relates to compounds of formula (I) wherein U, V, W, X, R1, R2, R3, R4, R5, R6, A, B, D, E, G, m, and n are as defined in the description, to pharmaceutically acceptable salts of such compounds for use in the manufacture of a medicament for the prevention or treatment of a bacterial infection. Certain compounds of formula (I) are new and are also part of this invention.
    本发明涉及式(I)的化合物,其中U、V、W、X、R1、R2、R3、R4、R5、R6、A、B、D、E、G、m和n的定义如说明书中所述,还涉及用于制造预防或治疗细菌感染的药物的上述化合物的药用可接受盐。式(I)中的某些化合物是新颖的,也是本发明的一部分。
  • [EN] PYRAZOLO-TRIAZINE AND/OR PYRAZOLO-PYRIMIDINE DERIVATIVES AS SELECTIVE INHIBITOR OF CYCLIN DEPENDENT KINASE<br/>[FR] DÉRIVÉS DE PYRAZOLO-TRIAZINE ET/OU DE PYRAZOLO-PYRIMIDINE EN TANT QU'INHIBITEURS SÉLECTIFS DE KINASE DÉPENDANTE DE LA CYCLINE
    申请人:QURIENT CO LTD
    公开号:WO2019197549A1
    公开(公告)日:2019-10-17
    The present invention relates to pyrazolo[1,5-a][1,3,5]triazine and pyrazolo[l,5-a]pyrimidine derivatives and/or pharmaceutically acceptable salts thereof, the use of these derivatives as pharmaceutically active agents, especially for the prophylaxis and/or treatment of cell proliferative diseases, inflammatory diseases, immunological diseases, cardiovascular diseases and infectious diseases. Furthermore, the present invention is directed towards pharmaceutical compositions containing at least one of the pyrazolo[1,5-a][1,3,5]triazine and pyrazolo[1,5-a]pyrimidine derivatives and/or pharmaceutically acceptable salts thereof.
    本发明涉及吡唑并[1,5-a][1,3,5]三嗪和吡唑[1,5-a]嘧啶衍生物和/或其药用可接受盐,以及这些衍生物作为药用活性剂的用途,特别是用于预防和/或治疗细胞增殖性疾病、炎症性疾病、免疫性疾病、心血管疾病和传染病。此外,本发明还涉及含有至少一种吡唑并[1,5-a][1,3,5]三嗪和吡唑[1,5-a]嘧啶衍生物和/或其药用可接受盐的药物组合物。
  • Monocyclic heterocycles as kinase inhibitors
    申请人:Borzilleri M. Robert
    公开号:US20050245530A1
    公开(公告)日:2005-11-03
    The present invention is directed to compounds having the formula and methods for using them for the treatment of cancer.
    本发明涉及具有以下公式化合物的用途以及使用它们治疗癌症的方法。
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