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4-羟基-6-甲基烟酸 | 67367-33-3

中文名称
4-羟基-6-甲基烟酸
中文别名
4-羟基-6-甲基-3-吡啶甲酸;6-甲基-4-羟基-3-吡啶甲酸;6-甲基-4-羟基-3-吡啶羧酸;头孢匹胺中间体
英文名称
4-hydroxy-6-methylnicotinic acid
英文别名
6-methyl-4-oxo-1H-pyridine-3-carboxylic acid
4-羟基-6-甲基烟酸化学式
CAS
67367-33-3
化学式
C7H7NO3
mdl
MFCD04038153
分子量
153.137
InChiKey
AOJLDZLRTUWFFY-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:
    263-265°C
  • 沸点:
    481.1±45.0 °C(Predicted)
  • 密度:
    1.393
  • 稳定性/保质期:
    远离氧化物。

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.142
  • 拓扑面积:
    66.4
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • WGK Germany:
    3
  • 海关编码:
    2933399090
  • 危险品标志:
    Xi
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H315,H319,H335
  • 储存条件:
    存放在密封容器中,并置于阴凉、干燥处。请确保存储地点远离氧化剂。

SDS

SDS:26f2aedcaa15505a4026368ac7900f75
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 4-Hydroxy-6-methylnicotinic acid
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 4-Hydroxy-6-methylnicotinic acid
CAS number: 67367-33-3

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: C7H7NO3
Molecular weight: 153.1

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

制备方法与用途

用途:主要用来合成头孢匹胺和头孢酚苄唑等药物。

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

反应信息

  • 作为反应物:
    描述:
    4-羟基-6-甲基烟酸一氯化碘calcium carbonate三氯氧磷 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 生成 Methyl 4-chloro-3-iodo-2-methyl-5-pyridinecarboxylate
    参考文献:
    名称:
    Pyrazolopyridinones as functionally selective GABAA ligands
    摘要:
    2,5-Dihydro-3H-pyrazolo[4,3-c]pyridin-3-ones are GABA(A) receptor benzodiazepine binding site ligands, which can exhibit functional selectivity for the alpha(3) subtype over the alpha(1), subtype. SAR studies to optimize this functional selectivity are described. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.08.006
  • 作为产物:
    描述:
    2-甲基-4-氨基吡啶硫酸potassium carbonate 、 sodium nitrite 作用下, 190.0~200.0 ℃ 、6.37 MPa 条件下, 生成 4-羟基-6-甲基烟酸
    参考文献:
    名称:
    Bojarska-Dahlig; Gruda, Roczniki Chemii, 1957, vol. 31, p. 1147,1151
    摘要:
    DOI:
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文献信息

  • [EN] SUBSTITUTED 4-PYRIDONES AND THEIR USE AS INHIBITORS OF NEUTROPHIL ELASTASE ACTIVITY<br/>[FR] 4-PYRIDONES SUBSTITUÉES ET LEUR UTILISATION COMME INHIBITEURS DE L'ACTIVITÉ DE L'ÉLASTASE NEUTROPHILE
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2014029831A1
    公开(公告)日:2014-02-27
    This invention relates to substituted 4-pyridones of formula 1 and their use as inhibitors of neutrophil elastase activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of pulmonary, gastrointestinal and genitourinary diseases, inflammatory diseases of the skin and the eye and other auto-immune and allergic disorders, allograft rejection, and oncological diseases.
    这项发明涉及式1的取代4-吡啶酮及其作为中性粒细胞弹性蛋白酶活性抑制剂的用途,含有这些化合物的药物组合物,以及将其用作治疗和/或预防肺部、胃肠道和泌尿系统疾病、皮肤和眼部炎症性疾病以及其他自身免疫和过敏性疾病、移植物排斥和肿瘤性疾病的药剂的方法。
  • SUBSTITUTED 4-PYRIDONES AND THEIR USE AS INHIBITORS OF NEUTROPHIL ELASTASE ACTIVITY
    申请人:OOST Thorsten
    公开号:US20140057916A1
    公开(公告)日:2014-02-27
    This invention relates to substituted 4-pyridones of formula 1 and their use as inhibitors of neutrophil elastase activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of pulmonary, gastrointestinal and genitourinary diseases, inflammatory diseases of the skin and the eye and other auto-immune and allergic disorders, allograft rejection, and oncological diseases.
    这项发明涉及式1的取代4-吡啶酮及其作为中性粒细胞弹性蛋白酶活性抑制剂的用途,包含这些化合物的药物组合物,以及将其用作治疗和/或预防肺部、胃肠道和泌尿系统疾病、皮肤和眼睛的炎症性疾病以及其他自身免疫和过敏性疾病、移植物排斥反应和肿瘤性疾病的药剂的方法。
  • [EN] NRF2 REGULATORS<br/>[FR] RÉGULATEURS DE NRF2
    申请人:GLAXOSMITHKLINE IP DEV LTD
    公开号:WO2016203401A1
    公开(公告)日:2016-12-22
    The present invention relates to aryl analogs, pharmaceutical compositions containing them and their use as Nrf2 regulators.
    本发明涉及芳基类似物,含有它们的药物组合物以及它们作为Nrf2调节剂的用途。
  • [EN] 3-(2,3-DIHYDRO-1H-INDEN-5-YL)PROPANOIC ACID DERIVATIVES AND THEIR USE AS NRF2 REGULATORS<br/>[FR] DÉRIVÉS D'ACIDE PROPANOÏQUE 3-(2,3-DIHYDRO-1H-INDEN-5-YL) ET LEUR UTILISATION EN TANT QUE RÉGULATEURS DE NRF2
    申请人:GLAXOSMITHKLINE IP DEV LTD
    公开号:WO2018104766A1
    公开(公告)日:2018-06-14
    The present invention relates to compounds of Formula (I), and Formula (II), wherein B is benzotriazolyl, phenyl, triazolopyridinyl, or -(CH2)2-triazolyl each of which may be unsubstituted or substituted by 1, 2, or 3 substituents independently chosen from -C1-3 alkyl, -O-C1-3 alkyl, CN, - (CH2)2-O-(CH2)2-OR4 and halo; and D is -C(O)OH, -C(O)NHSO2CH3, -SO2NHC(O)CH3, 5-(trifluoromethyl)-4H-1,2,4-triazol-2-yl, or tetrazolyl; and their use as NRF2 regulators.
    本发明涉及式(I)和式(II)的化合物,其中B为苯并三唑基、苯基、三唑吡啶基或-(CH2)2-三唑基,每种基团可以是未取代的或被1、2或3个取代基取代,所述取代基独立地选自-C1-3烷基、-O-C1-3烷基、CN、-(CH2)2-O-(CH2)2-OR4和卤素;D为-C(O)OH、-C(O)NHSO2CH3、-SO2NHC(O)CH3、5-(三氟甲基)-4H-1,2,4-三唑-2-基或四唑基;以及它们作为NRF2调节剂的用途。
  • CONDENSED LACTAM DERIVATIVE
    申请人:Sumitomo Dainippon Pharma Co., Ltd.
    公开号:US20200172543A1
    公开(公告)日:2020-06-04
    The present invention relates to a medicament for treating neuropsychiatric diseases, comprising a compound of Formula (1): or a pharmaceutically acceptable salt thereof, as an active ingredient.
    本发明涉及一种用于治疗神经精神疾病的药物,包括以下化合物(1)的药物学上可接受的盐,作为活性成分。
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