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5-羟基-2-吡啶羧酸 | 15069-92-8

中文名称
5-羟基-2-吡啶羧酸
中文别名
5-羟基吡啶羧酸;5-羟基吡啶-4-羧酸;5-羟基-2-吡啶甲酸5-HYDROXY-2-PYRIDINECARBOXYLICACID;5-羟基吡啶-2-甲酸;5-羟基-2-吡啶甲酸;5-羟基吡啶甲酸;5-羟基吡啶-2-羧酸
英文名称
5-hydroxypicolinic acid
英文别名
5-hydroxypyridine-2-carboxylic acid;5-Hydroxypicolinsaeure;5-hydroxy-2-pyridinecarboxylic acid
5-羟基-2-吡啶羧酸化学式
CAS
15069-92-8
化学式
C6H5NO3
mdl
MFCD00661309
分子量
139.111
InChiKey
CGRRUFNHHQCLDZ-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:
    260-264
  • 沸点:
    514.9±35.0 °C(Predicted)
  • 密度:
    1.485±0.06 g/cm3(Predicted)
  • 溶解度:
    易溶于丙酮、二甲基亚砜、乙醇和甲醇。
  • 最大波长(λmax):
    327nm(MeOH)(lit.)

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 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:
    70.4
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • 危险品标志:
    Xi
  • 安全说明:
    S26,S36/37/39
  • 危险类别码:
    R36/37/38
  • WGK Germany:
    3
  • 海关编码:
    2933399090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H315,H319,H335

SDS

SDS:a7bcdab76d7cfba38af1b2d268eafdd6
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Material Safety Data Sheet

Section 1. Identification of the substance
5-Hydroxypicolinic acid
Product Name:
Synonyms: 5-Hydroxy-2-pyridinecarboxylic acid

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H315: Causes skin irritation
H319: Causes serious eye irritation
H335: May cause respiratory irritation
P261: Avoid breathing dust/fume/gas/mist/vapours/spray
Wear protective gloves/protective clothing/eye protection/face protection
P280:
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.
5-Hydroxypicolinic acid
Ingredient name:
CAS number: 15069-92-8

Section 4. First aid measures
Immediately wash skin with copious amounts of water for at least 15 minutes while removing
Skin contact:
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.
Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.
Ingestion:

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: C6H5NO3
Molecular weight: 139.1

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
    • 1
    • 2
    • 3

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    34.对吡啶化学的贡献。第二部分 3-和5-羟基-2-甲基吡啶,以及5-羟基-2-甲基吡啶与甲醛在碱性介质中的缩合
    摘要:
    DOI:
    10.1039/jr9470000132
  • 作为产物:
    描述:
    5-氨基-2-吡啶羧酸硫酸 、 sodium nitrite 作用下, 生成 5-羟基-2-吡啶羧酸
    参考文献:
    名称:
    Oehlke, J.; Schroetter, E.; Dove, S., Pharmazie, 1983, vol. 38, # 9, p. 591 - 596
    摘要:
    DOI:
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文献信息

  • [EN] QUINOLINE AND QUINAZOLINE COMPOUNDS<br/>[FR] COMPOSÉS QUINOLÉINE ET QUINAZOLINE
    申请人:ACERTA PHARMA BV
    公开号:WO2016055982A1
    公开(公告)日:2016-04-14
    In some embodiments, the invention relates to quinazoline and quinoline compounds of Formula I: (I) or a pharmaceutically acceptable salt thereof, or to pharmaceutical compositions comprising these compounds and to their use in therapy. In particular, in some embodiments, the present invention relates to quinazoline and quinoline compounds, pharmaceutical compositions thereof, and the use of the compounds and pharmaceutical compositions in the treatment of Bruton's tyrosine kinase (BTK) mediated disorders.
    在某些实施例中,该发明涉及式I的喹唑啉和喹啉化合物:(I)或其药用可接受盐,或者涉及包含这些化合物的药物组合物以及它们在治疗中的应用。具体而言,在某些实施例中,本发明涉及喹唑啉和喹啉化合物、其药物组合物以及这些化合物和药物组合物在治疗布鲁顿氨基酸激酶(BTK)介导的疾病中的应用。
  • HETEROCYCLIC ANTIVIRAL COMPOUNDS
    申请人:Broka Chris Allen
    公开号:US20110070190A1
    公开(公告)日:2011-03-24
    The invention discloses 1-N-substituted-6-(hetero)aryl-1H-thieno[3,2-d]pyrimidin-4-one derivatives of formula wherein R 1 , R 2 , R 3 and R 4 are as defined herein that inhibit Hepatitis C virus NS5b polymerase inhibitors. Also disclosed are compositions and methods for treating an HCV infection and inhibiting HCV replication.
    该发明揭示了公式的1-N-取代-6-(杂)芳基-1H-噻吩[3,2-d]嘧啶-4-酮衍生物 其中R 1 ,R 2 ,R 3 和R 4 如本文所定义,抑制丙型肝炎病毒NS5b聚合酶抑制剂。还公开了治疗HCV感染和抑制HCV复制的组合物和方法。
  • DERIVATIVES OF N-ACYL-N'-PHENYLPIPERAZINE USEFUL (INTER ALIA) FOR THE PROPHYLAXIS OR TREATMENT OF DIABETES
    申请人:Kasai Shizuo
    公开号:US20120071489A1
    公开(公告)日:2012-03-22
    The present invention relates to a compound represented by the formula wherein each symbol is as defined in the present specification, which has a superior RBP4-lowering action and is useful as a pharmaceutical composition for the prophylaxis or treatment of a disease or condition mediated by an increase in RBP4.
    本发明涉及一种化合物,其化学式如下所示,其中每个符号如本说明书中所定义,该化合物具有优越的降低RBP4作用,并且可用作预防或治疗由RBP4增加介导的疾病或病况的药物组合物。
  • [EN] BICYCLIC HYDROXAMIC ACIDS USEFUL AS INHIBITORS OF MAMMALIAN HISTONE DEACETYLASE ACTIVITY<br/>[FR] ACIDES HYDROXAMIQUES BICYCLIQUES UTILES COMME INHIBITEURS DE L'ACTIVITÉ HISTONE DÉSACÉTYLASE CHEZ LE MAMMIFÈRE
    申请人:KANCERA AB
    公开号:WO2017108282A1
    公开(公告)日:2017-06-29
    A compound of formula (Ia) or (Ib) or a pharmaceutically acceptable salt thereof. The compound is an inhibitor of a histone deacetylase, and as such is useful in terepy, e.g. in the treatment of autoimmune disorders, mental disorders, neurodegenerative disorders, and hyperproliferative disorders.
    化合物的化学式(Ia)或(Ib)或其药学上可接受的盐。该化合物是组蛋白去乙酰化酶的抑制剂,因此在治疗自身免疫性疾病、精神障碍、神经退行性疾病和过度增生性疾病等方面非常有用。
  • [EN] SUBSTITUTED CONDENSED THIOPHENES AS MODULATORS OF STING<br/>[FR] THIOPHÈNES CONDENSÉS SUBSTITUÉS UTILISÉS EN TANT QUE MODULATEURS DE STING
    申请人:CTXT PTY LTD
    公开号:WO2019219820A1
    公开(公告)日:2019-11-21
    A compound of formula (I), wherein: R1 is selected from (i) H, (ii) C3-6cycloalkyl, (iii) C3-7heterocyclyl optionally substituted with a group selected from: methyl and ester, and (iv) linear or branched C1-4alkyl optionally substituted with a group selected from: alkoxy, amino, amido, acylamido, acyloxy, alkyl carboxyl ester, alkyl carbamoyl, alkyl carbamoyl ester, phenyl, phosphonate ester, C3-7heterocyclyl optionally substituted with a group selected from methyl and oxo, and a naturally occurring amino acid, optionally N-substituted with a group selected from methyl, acetyl and boc; A1 is CRA or N; A2 is CRB or N; A3 is CRC or N; A4 is CRD or N; where no more than two of A1, A2, A3, and A4 may be N; one or two of RA, RB, RC, and RD, (if present) are selected from H, F, Cl, Br, Me, CF3, cyclopropyl, cyano, OMe, OEt, CH2OH, CH2OMe and CH2NMe2; the remainder of RA, RB, RC, and RD, (if present) are H; Y is O, NH or CH2; RY is selected from: (RYA) and (RYB).
    化合物的化学式(I),其中:R1选自(i)H,(ii)C3-6环烷基,(iii)C3-7杂环烷基,可选择地取代为:甲基和酯,以及(iv)线性或支链C1-4烷基,可选择地取代为:烷氧基,氨基,酰胺基,酰氧基,烷基羧酯,烷基氨基,烷基氨基酯,苯基,磷酸酯,C3-7杂环烷基,可选择地取代为甲基和氧代基,以及一种天然氨基酸,可选择地N-取代为:甲基,乙酰基和boc;A1为CRA或N;A2为CRB或N;A3为CRC或N;A4为CRD或N;其中A1,A2,A3和A4中最多有两个可以是N;RA,RB,RC和RD中的一个或两个(如果存在)选自H,F,Cl,Br,Me,CF3,环丙基,氰基,OMe,OEt,CH2OH,CH2OMe和CH2NMe2;RA,RB,RC和RD的其余部分(如果存在)为H;Y为O,NH或CH2;RY选自:(RYA)和(RYB)。
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