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3-氯-5-羟基苯甲醛 | 1829-33-0

中文名称
3-氯-5-羟基苯甲醛
中文别名
一缩二乙二醇一(2-乙基已基)醚;二甘醇(2-乙己基)醚;2-乙己基卡必醇;二甘醇一(2-乙己基)醚;二乙二醇单辛醚;一缩二乙二醇单(2-乙基已基)醚;2-{(2-[(2-乙基己基)氧基]乙氧基}乙醇;二甘醇单(2-乙己基)醚
英文名称
3-chloro-5-hydroxybenzaldehyde
英文别名
——
3-氯-5-羟基苯甲醛化学式
CAS
1829-33-0
化学式
C7H5ClO2
mdl
MFCD08234659
分子量
156.569
InChiKey
BJENCCAVAIAGOF-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:
    104 °C
  • 沸点:
    268.3±20.0 °C(Predicted)
  • 密度:
    1.404±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 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:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2913000090
  • 危险性防范说明:
    P280,P305+P351+P338,P310
  • 危险性描述:
    H302,H315,H319,H332,H335
  • 储存条件:
    温度控制在2至8℃,采用惰性气体保护。

SDS

SDS:1cd9ec83f105b5421b95f73fe6e4c5ad
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 3-Chloro-5-hydroxybenzaldehyde
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 3-Chloro-5-hydroxybenzaldehyde
CAS number: 1829-33-0

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: C7H5ClO2
Molecular weight: 156.6

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, hydrogen chloride.

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:
    3-氯-5-羟基苯甲醛咪唑 、 palladium on activated charcoal 、 氢气 、 sodium hydride 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 生成
    参考文献:
    名称:
    细菌铁蛋白(BfrB)-铁氧还蛋白(Bfd)复合物的小分子抑制剂杀死包埋生物膜的铜绿假单胞菌细胞
    摘要:
    细菌依赖于良好调节的铁稳态以在不利环境中生存。铁稳态机制的关键组成部分是细菌铁蛋白中Fe 3+的区室化,以及随后以Fe 2+的形式动员以满足代谢需求。在铜绿假单胞菌中, Fe 3+在细菌铁蛋白(BfrB)中区分开,并且其动员到细胞质中需要结合铁氧还蛋白(Bfd)以减少储存的Fe 3+并释放可溶性Fe 2+。通过缺失bfd基因来阻断铜绿假单胞菌中的BfrB-Bfd复合物触发Fe 3+的不可逆积累在BfrB中,伴有胞质铁缺乏和生物膜发育的显着损害。本文中我们报道了发展为在Bfd结合位点结合BfrB的小分子会阻断BfrB-Bfd复合物,抑制铜绿假单胞菌细胞中BfrB的铁动员,对浮游细胞产生抑菌作用,并对嵌入其中的细胞具有杀菌作用。成熟的生物膜。
    DOI:
    10.1021/acsinfecdis.0c00669
  • 作为产物:
    描述:
    3-氯-5-羟基苯甲腈吡啶 、 sodium hypophosphite monohydrate 、 溶剂黄146 作用下, 以 为溶剂, 反应 1.0h, 以84%的产率得到3-氯-5-羟基苯甲醛
    参考文献:
    名称:
    AZAINDOLE DERIVATIVES AND THEIR USE AS ERK KINASE INHIBITORS
    摘要:
    本发明涉及一种化合物,其化学式为(I),或其药学上可接受的盐之一,特别用作激酶ERK活性,特别是ERK2活性的抑制剂。
    公开号:
    EP3170822A1
  • 作为试剂:
    描述:
    5-硝基-2-吡啶羧酸3-氯-5-羟基苯甲醛 、 sodium tetrahydroborate 、 palladium 10% on activated carbon 、 氢气 、 sodium hydroxide 作用下, 以 甲醇1,2-二氯乙烷 为溶剂, 反应 56.0h, 生成 5-(3,5-dichloro-2-methylbenzylamine)-2-pyridylcarboxylic acid
    参考文献:
    名称:
    作为神经保护剂的药用化合物
    摘要:
    本发明公开了一类作为神经保护剂的药用化合物,其为神经元型一氧化氮合酶‑突触后密度蛋白‑95(nNOS‑PSD95)的解耦联剂,其为具有通式(Ⅰ)苯环衍生物或其药学上可接受的盐。本申请进一步公开了该类化合物的制备方法以及其用于预防和治疗受神经元损伤影响引起的疾病的用途。
    公开号:
    CN104045552B
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文献信息

  • [EN] PYRAZOLOPYRIMIDIN-2-YL DERIVATIVES AS JAK INHIBITORS<br/>[FR] DÉRIVÉS DE PYRAZOLOPYRIMIDIN-2-YLE UTILISÉS COMME INHIBITEURS DE JAK
    申请人:ALMIRALL SA
    公开号:WO2015086693A1
    公开(公告)日:2015-06-18
    New pyrazolopyridmiin-2-yl derivatives are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Janus Kinases (JAK).
    新的吡唑吡啶-2-基衍生物被披露;以及它们的制备方法,包含它们的药物组合物以及它们作为Janus激酶(JAK)抑制剂在治疗中的用途。
  • [EN] PYRAZOLE MAGL INHIBITORS<br/>[FR] INHIBITEURS PYRAZOLE DE MAGL
    申请人:ABIDE THERAPEUTICS INC
    公开号:WO2018217805A1
    公开(公告)日:2018-11-29
    Provided herein are pyrazole compounds and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful as modulators of monoacylglycerol lipase (MAGL). Furthermore, the subject compounds and compositions are useful for the treatment of pain.
    本文提供了吡唑化合物和包含该化合物的药物组合物。这些化合物和组合物可用作单酰基甘油酶(MAGL)的调节剂。此外,这些化合物和组合物可用于治疗疼痛。
  • Mandelic acid derivatives and their use as throbin inhibitors
    申请人:——
    公开号:US20040019033A1
    公开(公告)日:2004-01-29
    There is provided a compound of formula I 1 wherein R a , R 1 , R 2 , Y and R 3 have meanings given in the description and pharmaceutically acceptable derivatives (including prodrugs) thereof, which compounds and derivatives are useful as, or are useful as prodrugs of, competitive inhibitors of trypsin-like proteases, such as thrombin, and thus, in particular, in the treatment of conditions where inhibition of thrombin is required (e.g. thrombosis) or as anticoagulants.
    提供了一种公式I的化合物 1 其中R a , R 1 , R 2 , Y和R 3 具有说明书中给出的含义以及药学上可接受的衍生物(包括前药),这些化合物和衍生物可用作竞争性胰蛋白酶样蛋白酶抑制剂,如凝血酶,因此,特别是用于需要抑制凝血酶的情况(例如血栓形成)或作为抗凝剂。
  • COFERONS AND METHODS OF MAKING AND USING THEM
    申请人:Barany Francis
    公开号:US20120295874A1
    公开(公告)日:2012-11-22
    The present invention is directed to a monomer useful in preparing therapeutic compounds. The monomer includes one or more pharmacophores which potentially binds to a target molecule with a dissociation constant of less than 300 μM and a linker element connected to the pharmacophore. The linker element has a molecular weight less than 500 daltons, is connected, directly or indirectly through a connector, to the pharmacophore.
    本发明涉及一种用于制备治疗性化合物的单体。该单体包括一个或多个可与目标分子结合的药效团,其解离常数小于300微摩尔,以及与药效团连接的连接元素。所述连接元素的分子量小于500道尔顿,通过直接连接或通过连接器间接与药效团相连。
  • [EN] PHARMACEUTICAL COMBINATION<br/>[FR] COMBINAISON PHARMACEUTIQUE
    申请人:ASTRAZENECA AB
    公开号:WO2003101956A1
    公开(公告)日:2003-12-11
    There is provided a combination product comprising: (1) a compound of claim 1 in WO 02/44145 or a compound of claim 20 in WO 02/44145 (or derivative thereof)or a pharmaceutically-acceptable derivative thereof; and (1) a compound as defined in claim 1 of WO 01/28992 or (2) a compound of Claim 34 of WO 01/28992 or (3) Compound A or B or C or D (or pharmaceutically-acceptable salts thereof) for use in treating arrhythmia or a coagulation controlled complication thereof.
    提供了一种组合产品,包括:(1) WO 02/44145中权利要求1的化合物或WO 02/44145中权利要求20的化合物(或其衍生物)或药用可接受的衍生物;以及(1)WO 01/28992中权利要求1定义的化合物或(2)WO 01/28992中权利要求34的化合物或(3)化合物A或B或C或D(或药用可接受的盐)用于治疗心律不齐或其凝血控制的并发症。
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