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5-氟烟酰胺 | 70-58-6

中文名称
5-氟烟酰胺
中文别名
——
英文名称
5-fluoronicotinamide
英文别名
5-fluoropyridine-3-carboxamide
5-氟烟酰胺化学式
CAS
70-58-6
化学式
C6H5FN2O
mdl
——
分子量
140.117
InChiKey
GCDSJMZGWCQCRU-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:
    174 - 176°C
  • 溶解度:
    可溶于DMSO(少许)、甲醇(少许)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.2
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    56
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933399090

SDS

SDS:4c2e1e0a8c6fb84e521b47ad3933a191
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 5-Fluoronicotinamide
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 5-Fluoronicotinamide
CAS number: 70-58-6

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: C6H5FN2O
Molecular weight: 140.1

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 fluoride.

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:
    5-氟烟酰胺三乙胺三氟乙酸酐 作用下, 以 二氯甲烷 为溶剂, 反应 12.0h, 以86.3%的产率得到5-氟-3-氰基吡啶
    参考文献:
    名称:
    [EN] INDOLE AHR INHIBITORS AND USES THEREOF
    [FR] INHIBITEURS D'INDOLE AHR ET LEURS UTILISATIONS
    摘要:
    公开号:
    WO2018195397A3
  • 作为产物:
    描述:
    5-氟吡啶-3-甲酸甲酯甲醇 作用下, 生成 5-氟烟酰胺
    参考文献:
    名称:
    5-氟烟酸和5-氟烟酰胺的制备。
    摘要:
    DOI:
    10.1021/jo01154a021
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文献信息

  • [EN] CATHEPSIN CYSTEINE PROTEASE INHIBITORS<br/>[FR] INHIBITEURS DE PROTÉASES À CYSTÉINE DE TYPE CATHEPSINES
    申请人:MERCK SHARP & DOHME
    公开号:WO2015054038A1
    公开(公告)日:2015-04-16
    This invention relates to a novel class of compounds which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis.
    这项发明涉及一类新型化合物,它们是半胱氨酸蛋白酶抑制剂,包括但不限于对卡特普辛K、L、S和B的抑制剂。这些化合物可用于治疗需要抑制骨吸收的疾病,如骨质疏松症。
  • [EN] BIARYL DERIVATIVES AS YAP/TAZ-TEAD PROTEIN-PROTEIN INTERACTION INHIBITORS<br/>[FR] DÉRIVÉS BIARYLE EN TANT QU'INHIBITEURS D'INTERACTION PROTÉINE-PROTÉINE YAP/TAZ-TEAD
    申请人:NOVARTIS AG
    公开号:WO2021186324A1
    公开(公告)日:2021-09-23
    The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof; (I) a method for manufacturing said compound, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition comprising said compound.
    本发明提供了化合物(I)或其药学上可接受的盐;(I)制造所述化合物的方法及其治疗用途。本发明还提供了药理活性剂的组合物和包括所述化合物的药物组合。
  • [EN] CATHEPSIN CYSTEINE PROTEASE INHIBITORS<br/>[FR] INHIBITEURS DE CYSTÉINE-PROTÉASES DE TYPE CATHEPSINES
    申请人:MERCK SHARP & DOHME
    公开号:WO2015051479A1
    公开(公告)日:2015-04-16
    This invention relates to a novel class of compounds which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis.
    这项发明涉及一类新型化合物,这些化合物是半胱氨酸蛋白酶抑制剂,包括但不限于对卡特普辛K、L、S和B的抑制剂。这些化合物可用于治疗需要抑制骨吸收的疾病,如骨质疏松症。
  • [EN] NOVEL SUBSTITUTED PYRIDINE COMPOUNDS AS INDOLEAMINE 2,3-DIOXYGENASE (IDO) INHIBITORS<br/>[FR] NOUVEAUX COMPOSÉS PYRIDINE SUBSTITUÉS UTILISÉS EN TANT QU'INHIBITEURS DE L'INDOLÉAMINE 2,3-DIOXYGÉNASE (IDO)
    申请人:MERCK SHARP & DOHME
    公开号:WO2019027856A1
    公开(公告)日:2019-02-07
    Disclosed herein is a compound of formula (I), or a pharmaceutically acceptable salt thereof: (I). Also disclosed herein are uses of the compounds disclosed herein in the potential treatment or prevention of an IDO-associated disease or disorder. Also disclosed herein are compositions comprising a compound disclosed herein. Further disclosed herein are uses of the compositions in the potential treatment or prevention of an IDO-associated disease or disorder.
    本文披露了式(I)的化合物,或其药用盐:(I)。本文还披露了所述化合物在潜在的治疗或预防IDO相关疾病或疾病中的用途。本文还披露了包含所述化合物的组合物。本文还披露了所述组合物在潜在的治疗或预防IDO相关疾病或疾病中的用途。
  • 一种5-氟-3-氨基吡啶的制备方法
    申请人:上海卡洛化学有限公司
    公开号:CN109678793B
    公开(公告)日:2020-08-04
    本发明公开了一种5‑氟‑3‑氨基吡啶的制备方法,属于吡啶类化合物技术领域,其特点包括如下操作步骤:将5‑氟烟酰胺滴加到次卤酸盐溶液内,再在0‑100℃下搅拌直至TLC反应完成;降至室温后加入氢氧化钠溶液,继续搅拌20‑40min,过滤烘干后得到5‑氟‑3‑氨基吡啶固体。本发明不仅操作工艺安全,简单方便,生产设备要求不高,而且在保证产品质量和良好的产率的基础上,适合放大生产。
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