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5-嘧啶乙酸 | 5267-07-2

中文名称
5-嘧啶乙酸
中文别名
——
英文名称
2-(pyrimidin-5-yl)acetic acid
英文别名
5-Pyrimidineacetic acid;2-pyrimidin-5-ylacetic acid
5-嘧啶乙酸化学式
CAS
5267-07-2
化学式
C6H6N2O2
mdl
MFCD09608122
分子量
138.126
InChiKey
HEEUMCHKVXTQIP-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:
    172-173 °C
  • 沸点:
    315.1±17.0 °C(Predicted)
  • 密度:
    1.336±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.3
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.166
  • 拓扑面积:
    63.1
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2933599090
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335

SDS

SDS:6594451b1baceb38df3dbfeef79553d2
查看
Material Safety Data Sheet

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

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

Section 3. Composition/information on ingredients.
Ingredient name: 5-Pyrimidineacetic acid
CAS number: 5267-07-2

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: C6H6N2O2
Molecular weight: 138.1

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.

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
  • 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-嘧啶乙酸溶剂黄146三乙胺 、 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 3.0h, 生成 5-bromo-2-(pyrimidin-5-ylmethyl)-1H-benzo[d]imidazole
    参考文献:
    名称:
    [EN] BENZIMIDAZOLE INHIBITORS OF THE SODIUM CHANNEL
    [FR] INHIBITEURS DE TYPE BENZIMIDAZOLE DU CANAL SODIQUE
    摘要:
    本发明涉及用于治疗与电压门控离子通道功能相关的疾病的化合物,特别是与钠通道活性相关的疾病。更具体地说,本发明关注的是一类化合物(例如,符合任何一种公式(I)-(XIII)或表1中的化合物(1)-(236)),这些化合物可用于治疗多种疾病和状况。公式(I)
    公开号:
    WO2012116440A1
  • 作为产物:
    描述:
    methyl 2-(pyrimidin-5-yl)acetate 在 lithium hydroxide monohydrate 、 作用下, 以 四氢呋喃 为溶剂, 生成 5-嘧啶乙酸
    参考文献:
    名称:
    [EN] NUCLEAR TRANSPORT REGULATOR AND USE THEREOF
    [FR] RÉGULATEUR DE TRANSPORT NUCLÉAIRE ET SON UTILISATION
    [ZH] 核转运调节剂及其用途
    摘要:
    本公开涉及药物领域,具体地,本公开涉及一种如式(I)所示的化合物或式(I)所示化合物的立体异构体、互变异构体、代谢产物、药学上可接受的盐或它的前药,
    公开号:
    WO2023134629A1
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文献信息

  • [EN] IMIDAZOTRIAZINONE COMPOUNDS<br/>[FR] COMPOSÉS D'IMIDAZOTRIAZINONE
    申请人:ENVIVO PHARMACEUTICALS INC
    公开号:WO2013142269A1
    公开(公告)日:2013-09-26
    The present invention provides imidazotriazinone compounds which are inhibitors of phosphodiesterase 9 and pharmaceutically acceptable salt thereof. The present invention further provides processes, pharmaceutical compositions, pharmaceutical preparations and pharmaceutical use of the compounds in the treatment of PDE9 associated diseases or disorders in mammals, including humans.
    本发明提供了咪唑三唑酮化合物,它们是磷酸二酯酶9的抑制剂及其药用盐。本发明还提供了用于治疗哺乳动物,包括人类,PDE9相关疾病或疾病的过程、药物组成、药物制剂和化合物的药用。
  • [EN] HETEROCYCLIC INHIBITORS OF GLUTAMINASE<br/>[FR] INHIBITEURS HÉTÉROCYCLIQUES DE GLUTAMINASE
    申请人:CALITHERA BIOSCIENCES INC
    公开号:WO2013078123A1
    公开(公告)日:2013-05-30
    The invention relates to the heterocyclic compounds of Formula (I) as defined further herein, and pharmaceutical preparations thereof. The invention further relates to methods of treating cancer, immunological or neurological diseases using the heterocyclic compounds of the invention.
    本发明涉及式(I)定义的杂环化合物及其药物制剂。本发明进一步涉及使用本发明的杂环化合物治疗癌症、免疫性或神经疾病的方法。
  • [EN] MODULATORS OF INDOLEAMINE 2,3-DIOXYGENASE<br/>[FR] MODULATEURS D'INDOLAMINE 2,3-DIOXYGÉNASE
    申请人:GLAXOSMITHKLINE IP DEV LTD
    公开号:WO2017195149A1
    公开(公告)日:2017-11-16
    Provided are IDO inhibitor compounds of Formula I and pharmaceutically acceptable salts thereof, their pharmaceutical compositions, their methods of preparation, and methods for their use in the prevention and/or treatment of diseases.
    提供的是IDO抑制剂化合物,其化学式为I,以及它们的药用可接受盐,它们的药物组合物,它们的制备方法,以及它们在预防或治疗疾病中的用途。
  • ISOTOPICALLY ENRICHED PYRIMIDIN-5-YL ACETIC ACID DERIVATIVES AS CRTH2 ANTAGONISTS
    申请人:Ly Tai Wei
    公开号:US20110172250A1
    公开(公告)日:2011-07-14
    Provided herein are 2 H- and 13 C-enriched compounds of formula (I) or (II); wherein R is as defined herein, and wherein at least one hydrogen atom, in certain embodiments, three or more hydrogen atoms, are deuterium atoms or at least one carbon atom is a carbon-13 atom. Also provided are pharmaceutical compositions and methods using the 2 H- and 13 C-enriched compounds, useful for treating CRTH2-related diseases or disorders such as, for example, asthma, allergic rhinitis, atopic dermatitis, allergic conjuvatitis, Churg-Strauss syndrome, sinusitis, basophilic leukemia, chronic urticaria or basophilic leukocytosis.
    本文提供了公式(I)或(II)的2H-和13C富集化合物;其中R如本文所定义,并且在某些情况下,至少一个氢原子,甚至三个或更多个氢原子,是氘原子,或者至少一个碳原子是碳-13原子。还提供了使用这些2H-和13C富集化合物的药物组合物和方法,用于治疗CRTH2相关疾病或疾病,例如哮喘、过敏性鼻炎、特应性皮炎、过敏性结膜炎、Churg-Strauss综合症、鼻窦炎、嗜碱性白血病、慢性荨麻疹或嗜碱性白细胞增多症。
  • [EN] NOVEL VIRAL REPLICATION INHIBITORS<br/>[FR] NOUVEAUX INHIBITEURS DE RÉPLICATION VIRALE
    申请人:UNIV LEUVEN KATH
    公开号:WO2011015641A1
    公开(公告)日:2011-02-10
    The present invention relates to a series of novel compounds having antiviral activity, more specifically HIV (Human Immunodeficiency Virus) replication inhibiting properties. The invention also relates to methods for the preparation of such compounds, as well as to novel intermediates useful in one or more steps of such syntheses. The invention also relates to pharmaceutical compositions comprising an effective amount of such compounds as active ingredients. This invention further relates to the use of such compounds as medicines or in the manufacture of a medicament useful for the treatment of animals suffering from viral infections, in particular HIV infection. This invention further relates to methods for the treatment of viral infections in animals by the administration of a therapeutical amount of such compounds, optionally combined with one or more other drugs having antiviral activity.
    本发明涉及一系列具有抗病毒活性的新化合物,更具体地说是具有抑制HIV(人类免疫缺陷病毒)复制的特性。该发明还涉及制备这些化合物的方法,以及在这些合成步骤中使用的新中间体。该发明还涉及包含这些化合物作为活性成分的有效量的药物组合物。本发明进一步涉及将这些化合物用作药物或用于制造对患有病毒感染,特别是HIV感染的动物进行治疗的药物。本发明还涉及通过给动物投予这些化合物的治疗量,可选择地与具有抗病毒活性的一个或多个其他药物结合的方法来治疗动物的病毒感染。
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