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1-(4-甲氧基苯)-1-环丙羧酸 | 16728-01-1

中文名称
1-(4-甲氧基苯)-1-环丙羧酸
中文别名
1-(4-甲氧基苯基)-1-环丙烷羧酸;1-(4-甲氧基)-1-环丙烷羧酸
英文名称
1-(4-methoxyphenyl)-1-cyclopropanecarboxylic acid
英文别名
1-(4-methoxyphenyl)cyclopropanecarboxylic acid;1-(4-methoxyphenyl)cyclopropane-1-carboxylic acid
1-(4-甲氧基苯)-1-环丙羧酸化学式
CAS
16728-01-1
化学式
C11H12O3
mdl
MFCD00019223
分子量
192.214
InChiKey
WCPFQQHADRJANG-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:
    127-132 °C
  • 沸点:
    288.19°C (rough estimate)
  • 密度:
    1.1430 (rough estimate)
  • 溶解度:
    溶于甲醇
  • 稳定性/保质期:
    遵照规定使用和储存,则不会发生分解。

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 安全说明:
    S24/25
  • 海关编码:
    2918990090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335
  • 储存条件:
    存放于阴凉干燥处。

SDS

SDS:ee5286d44d282ff7b945f09cd541147b
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Name: 1-(4-Methoxyphenyl)-1-cyclopropanecarboxylic acid 97% Material Safety Data Sheet
Synonym: 1-(4-Methoxyphenyl)cyclopropane-1-carboxylic aci
CAS: 16728-01-1
Section 1 - Chemical Product MSDS Name:1-(4-Methoxyphenyl)-1-cyclopropanecarboxylic acid 97% Material Safety Data Sheet
Synonym:1-(4-Methoxyphenyl)cyclopropane-1-carboxylic aci

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
16728-01-1 1-(4-Methoxyphenyl)-1-cyclopropanecarb 97 240-788-5
Hazard Symbols: None Listed.
Risk Phrases: None Listed.

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
The toxicological properties of this material have not been fully investigated.
Potential Health Effects
Eye:
May cause eye irritation.
Skin:
May cause skin irritation.
Ingestion:
May cause irritation of the digestive tract. The toxicological properties of this substance have not been fully investigated.
Inhalation:
May cause respiratory tract irritation. The toxicological properties of this substance have not been fully investigated.
Chronic:
No information found.

Section 4 - FIRST AID MEASURES
Eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.
Skin:
Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse.
Ingestion:
Never give anything by mouth to an unconscious person. Get medical aid. Do NOT induce vomiting. If conscious and alert, rinse mouth and drink 2-4 cupfuls of milk or water.
Inhalation:
Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid.
Notes to Physician:

Section 5 - FIRE FIGHTING MEASURES
General Information:
As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear. During a fire, irritating and highly toxic gases may be generated by thermal decomposition or combustion.
Extinguishing Media:
Use water spray, dry chemical, carbon dioxide, or appropriate foam.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Sweep up, then place into a suitable container for disposal. Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Use with adequate ventilation. Avoid contact with eyes, skin, and clothing. Avoid ingestion and inhalation.
Storage:
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Facilities storing or utilizing this material should be equipped with an eyewash facility and a safety shower. Use adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 16728-01-1: Personal Protective Equipment Eyes: Wear appropriate protective eyeglasses or chemical safety goggles as described by OSHA's eye and face protection regulations in 29 CFR 1910.133 or European Standard EN166.
Skin:
Wear appropriate protective gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to prevent skin exposure.
Respirators:
A respiratory protection program that meets OSHA's 29 CFR 1910.134 and ANSI Z88.2 requirements or European Standard EN 149 must be followed whenever workplace conditions warrant respirator use.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Solid
Color: white
Odor: None reported.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 124.00 - 126.00 deg C
Autoignition Temperature: Not applicable.
Flash Point: Not applicable.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature: Not available.
Solubility in water: Not available.
Specific Gravity/Density: Not available.
Molecular Formula: C11H12O3
Molecular Weight: 192.21

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable under normal temperatures and pressures.
Conditions to Avoid:
Incompatible materials, strong oxidants.
Incompatibilities with Other Materials:
Oxidizing agents.
Hazardous Decomposition Products:
Carbon monoxide, irritating and toxic fumes and gases, carbon dioxide.
Hazardous Polymerization: Has not been reported.

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 16728-01-1 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
1-(4-Methoxyphenyl)-1-cyclopropanecarboxylic acid - Not listed by ACGIH, IARC, or NTP.

Section 12 - ECOLOGICAL INFORMATION


Section 13 - DISPOSAL CONSIDERATIONS
Dispose of in a manner consistent with federal, state, and local regulations.

Section 14 - TRANSPORT INFORMATION

IATA
Not regulated as a hazardous material.
IMO
Not regulated as a hazardous material.
RID/ADR
Not regulated as a hazardous material.

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: Not available.
Risk Phrases:
Safety Phrases:
S 24/25 Avoid contact with skin and eyes.
WGK (Water Danger/Protection)
CAS# 16728-01-1: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 16728-01-1 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 16728-01-1 is not listed on the TSCA inventory.
It is for research and development use only.


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:
    1-(4-甲氧基苯)-1-环丙羧酸吡啶盐酸盐 作用下, 反应 28.0h, 以80%的产率得到1-(4-羟基苯基)-环丙烷羧酸
    参考文献:
    名称:
    WO2006/44133
    摘要:
    公开号:
  • 作为产物:
    描述:
    1-(4-甲氧基苯)-1'-环丙腈 在 lithium hydroxide 作用下, 以 为溶剂, 反应 18.0h, 生成 1-(4-甲氧基苯)-1-环丙羧酸
    参考文献:
    名称:
    Lewis碱性硫族化物催化剂对环丙基二酯的亲电溴化反应
    摘要:
    已经开发了使用三苯基膦硫化物(Ph 3 PS)或二苯基硒化物(Ph 2 Se)作为路易斯碱性硫族化物催化剂的环丙基甲基二酯的高效且区域选择性的亲电子溴化反应。据观察,博士3 PS利于形成抗非对映体,并产生多功能γ内酯。有趣的是,当使用Ph 2 Se作为催化剂时,非对映选择性被逆转,其中偏爱合成产物而不是反产物。
    DOI:
    10.1002/adsc.201800886
  • 作为试剂:
    描述:
    4-甲氧基苯甲酰胺1-(4-甲氧基苯)-1-环丙羧酸 、 palladium diacetate 、 乙腈 作用下, 反应 18.0h, 以96%的产率得到4-甲氧基苯甲腈
    参考文献:
    名称:
    钯催化伯酰胺脱水形成腈的开发和利用。
    摘要:
    在Selectfluor的存在下,钯(II)催化剂可将伯酰胺高效且化学选择性地转化为腈。酰胺可以连接到芳环,杂芳环或脂族侧链上,并且该反应可耐受空间体积和电子修饰。含有三个谷氨酰胺基团的肽醇的脱水为每个谷氨酰胺残基提供了构效关系。因此,这种脱水可以通过合成突变与谷氨酰胺的丙氨酸扫描相似。
    DOI:
    10.1021/acs.orglett.8b02422
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文献信息

  • Compositions for Treatment of Cystic Fibrosis and Other Chronic Diseases
    申请人:Vertex Pharmaceuticals Incorporated
    公开号:US20150231142A1
    公开(公告)日:2015-08-20
    The present invention relates to pharmaceutical compositions comprising an inhibitor of epithelial sodium channel activity in combination with at least one ABC Transporter modulator compound of Formula A, Formula B, Formula C, or Formula D. The invention also relates to pharmaceutical formulations thereof, and to methods of using such compositions in the treatment of CFTR mediated diseases, particularly cystic fibrosis using the pharmaceutical combination compositions.
    本发明涉及含有上皮钠通道活性抑制剂与至少一种ABC转运蛋白调节剂化合物(A式、B式、C式或D式)的药物组合物。该发明还涉及这些药物配方,以及使用这些组合物治疗CFTR介导的疾病,特别是囊性纤维化的方法。
  • [EN] COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF BROMODOMAIN-CONTAINING PROTEINS<br/>[FR] COMPOSÉS ET PROCÉDÉS POUR LA DÉGRADATION CIBLÉE DE PROTÉINES CONTENANT UN BROMODOMAINE
    申请人:ARVINAS INC
    公开号:WO2017030814A1
    公开(公告)日:2017-02-23
    The present invention relates to bifunctional compounds, which find utility as modulators of targeted ubiquitination, especially inhibitors of a variety of polypeptides and other proteins which are degraded and/or otherwise inhibited by bifunctional compounds according to the present invention. In particular, the present invention is directed to compounds, which contain on one end a VHL ligand which binds to the ubiquitin ligase and on the other end a moiety which binds a target protein such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of that protein. The present invention exhibits a broad range of pharmacological activities associated with compounds according to the present invention, consistent with the degradation/inhibition of targeted polypeptides.
    本发明涉及双功能化合物,其作为靶向泛素化的调节剂具有实用性,特别是根据本发明抑制各种多肽和其他蛋白质的化合物。具体而言,本发明涉及一端含有结合泛素连接酶的VHL配体,另一端含有结合靶蛋白的基团的化合物,使得靶蛋白靠近泛素连接酶以促使该蛋白的降解(和抑制)。根据本发明的化合物表现出与靶向多肽的降解/抑制一致的广泛的药理活性。
  • COMPOSITIONS FOR TREATMENT OF CYSTIC FIBROSIS AND OTHER CHRONIC DISEASES
    申请人:Van Goor Fredrick F.
    公开号:US20110098311A1
    公开(公告)日:2011-04-28
    The present invention relates to pharmaceutical compositions comprising an inhibitor of epithelial sodium channel activity in combination with at least one ABC Transporter modulator compound of Formula A, Formula B, Formula C, or Formula D. The invention also relates to pharmaceutical formulations thereof, and to methods of using such compositions in the treatment of CFTR mediated diseases, particularly cystic fibrosis using the pharmaceutical combination compositions.
    本发明涉及包含上皮钠通道活性抑制剂与至少一种ABC转运蛋白调节剂化合物(A式、B式、C式或D式)的药物组合物。该发明还涉及这些药物配方,以及使用这些组合物治疗CFTR介导的疾病,特别是囊性纤维化的方法。
  • AZACYCLIC COMPOUNDS
    申请人:ACADIA Pharmaceuticals Inc.
    公开号:US20150259291A1
    公开(公告)日:2015-09-17
    Compounds and methods are provided for the treatment of disease conditions in which modification of serotonergic receptor activity has a beneficial effect. In the method, an effective amount of a compound is adminstered to a patient in need of such treatment.
    提供用于治疗修改血清素能受体活性具有有益效果的疾病状态的化合物和方法。在方法中,将有效量的化合物施用于需要此类治疗的病人。
  • [EN] MODULATORS OF ATP-BINDING CASSETTE TRANSPORTERS<br/>[FR] MODULATEURS DE TRANSPORTEURS DE TYPE CASSETTE DE LIAISON A L'ATP
    申请人:VERTEX PHARMA
    公开号:WO2005075435A1
    公开(公告)日:2005-08-18
    The present invention relates to modulators of ATP-Binding Cassette ('ABC') transporters or fragments thereof, including Cystic Fibrosis Transmembrane Conductance Regulator ('CFTR'), compositions thereof, and methods therewith. The present invention also relates to methods of treating ABC transporter mediated diseases using such modulators (I) or a pharmaceutically acceptable salt thereof, wherein: Ht is a 5-membered heteroaromatic ring containing 1-4 heteroatoms selected from O, S, N or NH, wherein said ring is optionally fused to a 6-membered monocyclic or 10-membered bicyclic carbocyclic or heterocyclic, aromatic or non-aromatic ring, wherein Ht is optionally substituted with w occurrences of -WRw, wherein w is 0-5; ring A is 3-7 membered monocyclic ring having 0-3 heteroatoms selected from O, S, N, or NH, wherein ring A is optionally substituted with q occurrences of QRQ; ring B is optionally fused to 5-6 membered carbocyclic or heterocyclic, aromatic or non-aromatic ring .
    本发明涉及ATP结合盒('ABC')转运蛋白或其片段的调节剂,包括囊性纤维化跨膜传导调节蛋白('CFTR'),以及相关的组合物和方法。本发明还涉及使用这些调节剂(I)或其药学上可接受的盐治疗ABC转运蛋白介导的疾病的方法,其中:Ht是含有1-4个来自O、S、N或NH的杂原子的5元杂芳环,其中所述环可选择地与含有0-5个-WRw的w出现的6元单环或10元双环碳环或杂环、芳香或非芳香环融合;环A是具有0-3个来自O、S、N或NH的杂原子的3-7元单环,其中环A可选择地与q出现的QRQ取代;环B可选择地与5-6元碳环或杂环、芳香或非芳香环融合。
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