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N-Cbz-3-哌啶甲醛 | 201478-72-0

中文名称
N-Cbz-3-哌啶甲醛
中文别名
N-苄氧羰基-3-哌啶甲醛;1-CBZ-3-哌啶甲醛
英文名称
benzyl 3-formylpiperidine-1-carboxylate
英文别名
1-Benzyloxycarbonylpiperidine-3-carboxaldehyde;benzyl 3-formyl-1-piperidinecarboxylate;3-formyl-piperidine-1-carboxylic acid benzyl ester;1-Benzyloxycarbonyl-3-formyl piperidine;3-formyl-N-Cbz-piperidine
N-Cbz-3-哌啶甲醛化学式
CAS
201478-72-0
化学式
C14H17NO3
mdl
MFCD02179022
分子量
247.294
InChiKey
QKGTVOXHDCVOAW-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:
    384.5±42.0 °C(Predicted)
  • 密度:
    1?+-.0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.428
  • 拓扑面积:
    46.6
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xi
  • 海关编码:
    2933399090
  • 危险性防范说明:
    P280,P305+P351+P338
  • 危险性描述:
    H302

SDS

SDS:05b6e54d8a715a96a429fe50690c54c9
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: Benzyl 3-formylpiperidine-1-carboxylate
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: Benzyl 3-formylpiperidine-1-carboxylate
CAS number: 201478-72-0

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: C14H17NO3
Molecular weight: 247.3

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

反应信息

  • 作为反应物:
    描述:
    N-Cbz-3-哌啶甲醛吡啶 、 palladium 10% on activated carbon 、 氢气碳酸氢钠磺酰胺 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 20.0 ℃ 、137.9 kPa 条件下, 反应 48.0h, 生成 1-benzyl-3-[(1,1-dioxido-1,2,5-thiadiazolidin-2-yl)methyl]piperidine
    参考文献:
    名称:
    环磺酰胺衍生物对诺沃克病毒的有效抑制
    摘要:
    已鉴定出一类在基于细胞的系统中表现出抗诺如病毒活性并在其结构中包含环磺酰胺支架的新化合物。初始命中的结构(化合物2a,ED 50 4 μM,TD 50 50 μM)已通过利用多个多样性点并生成适当的结构-活性关系进行了展望。
    DOI:
    10.1016/j.bmc.2011.08.054
  • 作为产物:
    描述:
    3-哌啶甲酸乙酯 在 lithium aluminium tetrahydride 、 2,2,6,6-四甲基哌啶氧化物碳酸氢钠 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 35.0h, 生成 N-Cbz-3-哌啶甲醛
    参考文献:
    名称:
    Carbazole inhibitors of histamine receptors for the treatment of disease
    摘要:
    本发明涉及咔唑化合物,包括它们的药物组合物,以及可能作为H1R和/或H4R的抑制剂用于治疗或预防炎症性、自身免疫性、过敏性和眼部疾病的方法。
    公开号:
    US08080566B1
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文献信息

  • Src kinase inhibitor compounds
    申请人:Merck & Co., Inc.
    公开号:US06498165B1
    公开(公告)日:2002-12-24
    Pyrimidine compounds (Formula I), or their pharmaceutically acceptable salts, hydrates, solvates, crystal forms and individual diastereomers, and pharmaceutical compositions including the same, which are inhibitors of tyrosine kinase enzymes, and as such are useful in the prophylaxis and treatment of protein tyrosine kinase-associated disorders, such as immune diseases, hyperproliferative disorders and other diseases in which inappropriate protein kinase action is believed to play a role, such as cancer, angiogensis, atheroscelerosis, graft rejection, rheumatoid arthritis and psoriasis.
    嘧啶化合物(化学式I),或其药用可接受的盐、水合物、溶剂合物、晶型和单一对映异构体,以及包括这些化合物的药物组合物,它们是酪氨酸激酶酶的抑制剂,因此在预防和治疗蛋白酪氨酸激酶相关疾病方面具有用处,如免疫疾病、高增殖性疾病和其他认为不当的蛋白激酶作用可能起作用的疾病,如癌症、血管生成、动脉粥样硬化、移植排斥、类风湿性关节炎和牛皮癣。
  • BENZOXAZEPIN COMPOUNDS SELECTIVE FOR PI3K P110 DELTA AND METHODS OF USE
    申请人:Heffron Timothy
    公开号:US20120245144A1
    公开(公告)日:2012-09-27
    Benzoxazepin Formula I compounds, including stereoisomers, geometric isomers, tautomers, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting the delta isoform of PI3K, and for treating disorders mediated by lipid kinases such as inflammation, immunological disorders, and cancer. 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.
    本句翻译为中文是:苯并恶唑啉I型化合物,包括立体异构体、几何异构体、互变异构体、代谢物以及药学上可接受的盐,对于抑制PI3K的δ异构体以及治疗由脂质激酶介导的疾病如炎症、免疫疾病和癌症是有用的。公开了使用I型化合物公式进行体外、原位和体内诊断、预防或治疗哺乳动物细胞中此类疾病或相关病理状况的方法。
  • [EN] GCN2 INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS DE GCN2 ET LEURS UTILISATIONS
    申请人:MERCK PATENT GMBH
    公开号:WO2019148132A1
    公开(公告)日:2019-08-01
    The present invention provides compounds, compositions thereof, and methods of using the same.
    本发明提供了化合物、其组合物以及使用它们的方法。
  • [EN] COMPOUNDS AND METHODS FOR THE TREATMENT OR PREVENTION OF FLAVIVIRUS INFECTIONS<br/>[FR] COMPOSES ET PROCEDES DE TRAITEMENT OU DE PREVENTION D'INFECTIONS A FLAVIVIRUS
    申请人:VIROCHEM PHARMA INC
    公开号:WO2004052885A1
    公开(公告)日:2004-06-24
    The present invention provides novel compounds represented by formula (I) or pharmaceutically acceptable salts thereof useful for treating flaviviridae viral infection.
    本发明提供了一种表示为式(I)的新化合物,或其在药学上可接受的盐,用于治疗黄病毒科病毒感染。
  • [EN] INHIBITORS OF PROTEIN KINASES<br/>[FR] INHIBITEURS DE PROTÉINE KINASES
    申请人:INGENIUM PHARMACEUTICALS GMBH
    公开号:WO2009047359A1
    公开(公告)日:2009-04-16
    Compounds of general Formula I, wherein R1, R2, R3, x, A and Ra are as defined herein are inhibitors of cyclin-dependent kinases and are useful for preventing and/or treating any type of pain, inflammatory disorders, immunological diseases, proliferative diseases, infectious diseases, cardiovascular diseases and neurodegenerative diseases.
    通式I的化合物,其中R1、R2、R3、x、A和Ra的定义如本文所述,是细胞周期依赖性激酶的抑制剂,可用于预防和/或治疗任何类型的疼痛、炎症性疾病、免疫性疾病、增殖性疾病、传染性疾病、心血管疾病和神经退行性疾病。
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