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3-氰基-5-羟基吡啶 | 152803-24-2

中文名称
3-氰基-5-羟基吡啶
中文别名
5-羟基烟腈
英文名称
5-hydroxynicotinonitrile
英文别名
5-hydroxypyridine-3-carbonitrile;3-cyano-5-hydroxypyridine
3-氰基-5-羟基吡啶化学式
CAS
152803-24-2
化学式
C6H4N2O
mdl
——
分子量
120.111
InChiKey
KAXIYYPIORYZLB-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:
    213-217℃
  • 沸点:
    394.7±27.0 °C(Predicted)
  • 密度:
    1.33±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.2
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    56.9
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险等级:
    6.1
  • 海关编码:
    2933399090
  • 危险性防范说明:
    P261,P301+P312,P302+P352,P304+P340,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335
  • 储存条件:
    2-8°C

SDS

SDS:0b21f5b7e7b341054d37a38f04fa3300
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 3-Cyano-5-hydroxypyridine
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H331: Toxic if inhaled
H302: Harmful if swallowed
H312: Harmful in contact with skin
Causes skin irritation
H315:
H319: Causes serious eye irritation
H335: May cause respiratory irritation
P261: Avoid breathing dust/fume/gas/mist/vapours/spray
P280: Wear protective gloves/protective clothing/eye protection/face protection
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present
and easy to do – continue rinsing
P304+P340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing
P405: Store locked up

Section 3. Composition/information on ingredients.
Ingredient name: 3-Cyano-5-hydroxypyridine
CAS number: 152803-24-2

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.
Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
Eye contact:
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.
Storage: Store in closed vessels.

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
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C6H4N2O
Molecular weight: 120.1

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
UN Number: UN3439 Class: 6.1 Packing group: III
Proper shipping name: NITRILES, TOXIC, SOLID, N.O.S. (3-Cyano-5-hydroxypyridine)

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:
    3-氰基-5-羟基吡啶N-氯代丁二酰亚胺 作用下, 以 乙腈 为溶剂, 以36%的产率得到6-chloro-5-hydroxynicotinonitrile
    参考文献:
    名称:
    Boron-Containing Small Molecules as Anti-Inflammatory Agents
    摘要:
    化合物和治疗抗炎症状况的方法被披露。
    公开号:
    US20150291629A1
  • 作为产物:
    描述:
    3-氰基吡啶-5-硼酸频哪醇酯 在 hydrazine hydrate 、 caesium carbonate 作用下, 以 为溶剂, 反应 16.0h, 以85%的产率得到3-氰基-5-羟基吡啶
    参考文献:
    名称:
    一种催化氧化芳硼类化合物制备酚的方法
    摘要:
    本发明公开了一种催化氧化芳硼类化合物合成酚类化合物的方法,在溶剂醇或醇的水溶液中,在碱的作用下,加入水合肼或肼类化合物催化剂,催化氧化芳硼类化合物直接制备酚类化合物。本发明的制备酚类化合物的方法,催化剂是廉价的水合肼或肼类化合物,氧化剂为常压下的空气或氧气,反应无需金属催化剂且活性好,底物来源广泛且稳定,底物敏感官能团相容性好且适用范围广。在优化的反应条件之下,目标产品分离收率高达99%。
    公开号:
    CN103936538B
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文献信息

  • DERIVATIVES OF AZAINDAZOLE OR DIAZAINDAZOLE TYPE AS MEDICAMENT
    申请人:PIERRE FABRE MEDICAMENT
    公开号:US20130085144A1
    公开(公告)日:2013-04-04
    The present invention relates to a compound of following formula (I): or a pharmaceutically acceptable salt or solvate of same, a tautomer of same, or a stereoisomer or mixture of stereoisomers of same in any proportions, such as a mixture of enantiomers, notably a racemic mixture; as well as to the use of same as a drug, notably intended for the treatment of cancer, inflammation and neurodegenerative diseases such as Alzheimer's disease; to the use of same as a kinase inhibitor; to the pharmaceutical compositions comprising same; and to methods for the preparation of same.
    本发明涉及以下式(I)的化合物: 或其药学上可接受的盐或溶剂,同分异构体,立体异构体或同分异构体的混合物,比如对映体混合物,尤其是消旋混合物;以及将其用作药物,尤其是用于治疗癌症、炎症和神经退行性疾病如阿尔茨海默病;将其用作激酶抑制剂;含有同样化合物的药物组合物;以及制备同样化合物的方法。
  • [EN] DERIVATIVES OF AZAINDAZOLE OR DIAZAINDAZOLE TYPE FOR TREATING PAIN<br/>[FR] DÉRIVÉS DE TYPE AZA-INDAZOLE OU DIAZA-INDAZOLE POUR LE TRAITEMENT DE LA DOULEUR
    申请人:PF MEDICAMENT
    公开号:WO2014016433A1
    公开(公告)日:2014-01-30
    The present invention relates to a compound of following formula (I): or a pharmaceutically acceptable salt or solvate of same, a tautomer of same, or a stereoisomer or mixture of stereoisomers of same in any proportions, such as a mixture of enantiomers, notably a racemic mixture; for use in the treatment of pain.
    本发明涉及如下式(I)的化合物:或其药用可接受的盐或溶剂化物,其构象异构体,或其立体异构体或立体异构体混合物,以任何比例,例如对映体混合物,尤其是外消旋混合物;用于治疗疼痛。
  • [EN] DERIVATIVES OF AZAINDAZOLE OR DIAZAINDAZOLE TYPE FOR TREATING A CANCER OVEREXPRESSING TRK<br/>[FR] DÉRIVÉS DE TYPE AZA-INDAZOLE OU DIAZA-INDAZOLE POUR LE TRAITEMENT D'UN CANCER SUREXPRIMANT LA TRK
    申请人:PF MEDICAMENT
    公开号:WO2014016434A1
    公开(公告)日:2014-01-30
    The present invention relates to a compound of following formula (I) or a pharmaceutically acceptable salt or solvate of same, a tautomer of same, or a stereoisomer or mixture of stereoisomers of same in any proportions, such as a mixture of enantiomers, notably a racemic mixture, as well as pharmaceutical composition comprising such a compound, for use in the treatment of a cancer associated with the overexpression of at least one Trk protein.
    本发明涉及式(I)所示的化合物,或其药用可接受的盐或溶剂化物,其同分异构体,或其立体异构体或立体异构体混合物,以任何比例,例如对映体混合物,尤其是外消旋混合物,以及包含该化合物的药物组合物,用于治疗与至少一种Trk蛋白过表达相关的癌症。
  • Derivatives of azaindazole or diazaindazole type for treating a cancer overexpressing trk
    申请人:PIERRE FABRE MEDICAMENT
    公开号:EP2689779A1
    公开(公告)日:2014-01-29
    The present invention relates to a compound of following formula (I): or a pharmaceutically acceptable salt or solvate of same, a tautomer of same, or a stereoisomer or mixture of stereoisomers of same in any proportions, such as a mixture of enantiomers, notably a racemic mixture, as well as pharmaceutical composition comprising such a compound, for use in the treatment of a cancer associated with the overexpression of at least one Trk protein.
    本发明涉及具有以下公式(I)的化合物: 或其药用可接受的盐或溶剂化物,其互变异构体,或其立体异构体或立体异构体混合物,以任何比例,如对映体混合物,尤其是外消旋混合物,以及包含该化合物的药物组合物,用于治疗与至少一种Trk蛋白过度表达相关的癌症。
  • [EN] ARYL ETHERS AND USES THEREOF<br/>[FR] ARYLÉTHERS ET UTILISATIONS DE CEUX-CI
    申请人:PELOTON THERAPEUTICS INC
    公开号:WO2015035223A1
    公开(公告)日:2015-03-12
    The present disclosure relates to HIF-2α inhibitors and methods of making and using them for treating cancer. Certain compounds were potent in HIF-2α scintillation proximity assay, luciferase assay, and VEGF ELISA assay, and led to tumor size reduction and regression in 786-O xenograft bearing mice in vivo.
    本公开涉及HIF-2α抑制剂及其制备和用于治疗癌症的方法。某些化合物在HIF-2α闪烁近距离法、荧光素酶法和VEGF ELISA法中表现出强效,导致786-O异种移植瘤小鼠体内肿瘤大小减小和回归。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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cnmr
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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