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3-甲酰基(1,1-联苯)-4-羧酸 | 222180-23-6

中文名称
3-甲酰基(1,1-联苯)-4-羧酸
中文别名
——
英文名称
3’-formyl-[1,1’-biphenyl]-4-carboxylic acid
英文别名
3'-formylbiphenyl-4-carboxylic acid;4-(3-formylphenyl)benzoic Acid
3-甲酰基(1,1-联苯)-4-羧酸化学式
CAS
222180-23-6
化学式
C14H10O3
mdl
——
分子量
226.232
InChiKey
ZIJAWDBNCZHVRY-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:
    231 °C

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xi
  • 海关编码:
    2918300090
  • 危险性防范说明:
    P264,P270,P280,P301+P312+P330,P305+P351+P338,P337+P313,P501
  • 危险性描述:
    H302,H319

SDS

SDS:18ba7191fdfb7d1d4ae1d609ac4cca65
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Name: 3 -Formyl[1 1 -biphenyl]-4-carboxylic acid Material Safety Data Sheet
Synonym: None Known
CAS: 222180-23-6
Section 1 - Chemical Product MSDS Name:3 -Formyl[1 1 -biphenyl]-4-carboxylic acid Material Safety Data Sheet
Synonym:None Known

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
222180-23-6 3'-Formyl[1,1'-biphenyl]-4-carboxylic 95+ unlisted
Hazard Symbols: XN
Risk Phrases: 20/21/22 36/37/38

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Harmful by inhalation, in contact with skin and if swallowed.
Irritating to eyes, respiratory system and skin.
Potential Health Effects
Eye:
Causes eye irritation. May cause chemical conjunctivitis.
Skin:
Causes skin irritation. Harmful if absorbed through the skin.
Ingestion:
Harmful if swallowed. May cause irritation of the digestive tract.
Inhalation:
Causes respiratory tract irritation. Harmful if inhaled.
Chronic:
No information found.

Section 4 - FIRST AID MEASURES
Eyes: Immediately 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. Wash mouth out with 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:
Treat symptomatically and supportively.

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.
Extinguishing Media:
Use water spray, dry chemical, carbon dioxide, or chemical foam.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Vacuum or sweep up material and place into a suitable disposal container. Clean up spills immediately, observing precautions in the Protective Equipment section. Avoid generating dusty conditions.
Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Minimize dust generation and accumulation. Avoid breathing dust, vapor, mist, or gas. Avoid contact with eyes, skin, and clothing.
Keep container tightly closed. Avoid ingestion and inhalation. Use with adequate ventilation. Wash clothing before reuse.
Storage:
Store in a cool, dry place. Store in a tightly closed container.

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# 222180-23-6: 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:
Follow the OSHA respirator regulations found in 29 CFR 1910.134 or European Standard EN 149. Use a NIOSH/MSHA or European Standard EN 149 approved respirator if exposure limits are exceeded or if irritation or other symptoms are experienced.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Solid
Color: off-white
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 231-233 deg C
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density:
Molecular Formula: C14H10O3
Molecular Weight: 226.23

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable at room temperature in closed containers under normal storage and handling conditions.
Conditions to Avoid:
Dust generation.
Incompatibilities with Other Materials:
Oxidizing agents, amines, bases.
Hazardous Decomposition Products:
Carbon monoxide, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 222180-23-6 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
3'-Formyl[1,1'-biphenyl]-4-carboxylic 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
Shipping Name: TOXIC SOLID, ORGANIC, N.O.S.
Hazard Class: 6.1
UN Number: 2811
Packing Group: III
IMO
Shipping Name: TOXIC SOLID, ORGANIC, N.O.S.
Hazard Class: 6.1
UN Number: 2811
Packing Group: III
RID/ADR
Shipping Name: TOXIC SOLID, ORGANIC, N.O.S.
Hazard Class: 6.1
UN Number: 2811
Packing group: III

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: XN
Risk Phrases:
R 20/21/22 Harmful by inhalation, in contact with
skin and if swallowed.
R 36/37/38 Irritating to eyes, respiratory system
and skin.
Safety Phrases:
S 22 Do not breathe dust.
S 26 In case of contact with eyes, rinse immediately
with plenty of water and seek medical advice.
S 36/37/39 Wear suitable protective clothing, gloves
and eye/face protection.
WGK (Water Danger/Protection)
CAS# 222180-23-6: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 222180-23-6 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 222180-23-6 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

反应信息

  • 作为反应物:
    描述:
    3-甲酰基(1,1-联苯)-4-羧酸间氯过氧苯甲酸 、 potassium hydroxide 作用下, 以 二氯甲烷甲醇 为溶剂, 反应 1.0h, 以28 mg的产率得到3,-羟基联苯-4-甲酸
    参考文献:
    名称:
    联苯-4-羧酸及其衍生物(即4-苯基水杨酸和5-苯基水杨酸)的光芬顿选择性和光催化羟基化反应
    摘要:
    使用部分TiO 2介导的光催化降解和光芬顿条件,确定了4-苯基苯甲酸,4-苯基水杨酸和5-苯基水杨酸的远端羟基化的选择性。结合位点与被羟基化的苯基的这种分离可以减少偏倚的评估。假定4-羧基苯基是一个略微吸电子的取代基,则羟基化区域化学反应的性质与亲电反应的定性一致。由于电子需求的逆转,同时吸附到TiO 2上,使4-和5-苯基水杨酸中远端苯基的羟化选择性逆转假定这两个结构的表面相似。版权所有©2011 John Wiley&Sons,Ltd.
    DOI:
    10.1002/poc.1839
  • 作为产物:
    描述:
    4-甲氧羰基苯硼酸四(三苯基膦)钯 、 sodium carbonate 、 lithium hydroxide 作用下, 以 四氢呋喃乙腈 为溶剂, 反应 36.0h, 生成 3-甲酰基(1,1-联苯)-4-羧酸
    参考文献:
    名称:
    [EN] HETEROCYCLIC INTEGRIN AGONISTS
    [FR] AGONISTES HÉTÉROCYCLIQUES D'INTÉGRINE
    摘要:
    本发明提供了多环氧硫代咪唑啉、二氧代咪唑啉、氧硫代氧咪唑啉、二氧代氧咪唑啉以及相关化合物,这些化合物可用作整合素激动剂。还描述了用于治疗整合素介导疾病如癌症的方法。
    公开号:
    WO2018126072A1
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文献信息

  • Amidocarboxylic acid derivatives
    申请人:Sankyo Company, Limited
    公开号:US06528525B1
    公开(公告)日:2003-03-04
    Amidocarboxylic acid derivatives of the formula: wherein R1 represents a hydrogen atom, etc.; R2 represents an alkylene group; R3 represents a hydrogen atom, etc.; R4 represents a hydrogen atom, etc.; X represents a substituted or unsubstituted aryl group, etc.,; Y represents an oxygen atom, etc.; Z represents an alkylene group, etc.; and W represents an alkyl group, etc.; and pharmacologically acceptable salts thereof and pharmacologically acceptable esters thereof are useful as the active ingredient of pharmaceutical compositions. They may be used to treat specified diseases, including diabetes mellitus, hyperlipemia, arteriosclerosis, hypertension, etc.
    公式为:其中R1代表氢原子,等等;R2代表烷基团;R3代表氢原子,等等;R4代表氢原子,等等;X代表取代或未取代的芳基团,等等;Y代表氧原子,等等;Z代表烷基团,等等;W代表烷基团,等等;以及其药理学上可接受的盐和药理学上可接受的酯作为药物组合物的活性成分是有用的。它们可用于治疗特定疾病,包括糖尿病、高脂血症、动脉硬化、高血压等。
  • [EN] MALE CONTRACEPTIVE COMPOSITIONS AND METHODS OF USE<br/>[FR] COMPOSITIONS CONTRACEPTIVES POUR LES HOMMES ET PROCÉDÉS D'UTILISATION ASSOCIÉS
    申请人:DANA FARBER CANCER INST INC
    公开号:WO2011143657A1
    公开(公告)日:2011-11-17
    The invention relates to compositions and methods for effecting male contraception.
    这项发明涉及用于实现男性避孕的组合物和方法。
  • [EN] COMPOSITIONS AND METHODS FOR MODULATING METABOLISM<br/>[FR] COMPOSITIONS ET PROCÉDÉS PERMETTANT DE MODULER UN MÉTABOLISME
    申请人:DANA FARBER CANCER INST INC
    公开号:WO2011143651A1
    公开(公告)日:2011-11-17
    The invention provides compositions comprising an effective amount of an agent that inhibits a BET protein (e.g., Brd2, Brd3, Brd4), and methods of using such compositions for treating or preventing metabolic syndrome, obesity, type II diabetes, insulin resistance, and related disorders characterized by undesirable alterations in metabolism or fat accumulation.
    本发明提供了含有效量抑制BET蛋白(例如Brd2、Brd3、Brd4)的药物的组合物,以及使用这样的组合物治疗或预防代谢综合征、肥胖症、2型糖尿病、胰岛素抵抗和与代谢或脂肪积累不良变化相关的疾病的方法。
  • PYRROL-1-YL BENZOIC ACID DERIVATIVES USEFUL AS MYC INHIBITORS
    申请人:DANA-FARBER CANCER INSTITUTE, INC.
    公开号:US20150291521A1
    公开(公告)日:2015-10-15
    The present invention provides compounds of Formula (I-A), (I-B), and (I-C), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting Myc (e.g., c-Myc) activity. The present invention further provides methods of using the compounds described herein for treating Myc-mediated disorders (e.g., cancer and other proliferative diseases). The present invention also provides assays for identifying Myc inhibitors.
    本发明提供了公式(I-A)、(I-B)和(I-C)的化合物,其药学上可接受的盐以及其制药组合物。本发明的化合物可用于抑制Myc(例如c-Myc)的活性。本发明还提供了使用本文所描述的化合物治疗Myc介导的疾病(例如癌症和其他增殖性疾病)的方法。本发明还提供了用于鉴定Myc抑制剂的检测方法。
  • Non-peptidic immunoproteasome β5i-selective inhibitor as potential treatment for idiopathic pulmonary fibrosis: Virtual screening, hit evolution and lead identification
    作者:Yunxuan Li、Guanglei Nan、Xianxin Hou、Yechao Yan、Yajun Yang、Ying Yang、Ke Li、Zhiyan Xiao
    DOI:10.1016/j.ejmech.2023.115856
    日期:2023.12
    The immunoproteasome has emerged as a potential therapeutic target for idiopathic pulmonary fibrosis (IPF). We report herein our efforts to discover novel non-peptidic immunoproteasome inhibitors as potential treatment for IPF. A structure-based virtual screening was initially performed and the hit compound VS-7 with an IC50 of 9.437 μM against β5i was identified. Hit evolution based on the interaction
    免疫蛋白酶体已成为特发性肺纤维化(IPF)的潜在治疗靶点。我们在此报告我们努力发现新型非肽免疫蛋白酶体抑制剂作为 IPF 的潜在治疗方法。最初进行了基于结构的虚拟筛选,并鉴定了针对 β5i 的IC 50为 9.437 μM的命中化合物VS-7 。基于VS-7相互作用模式的命中进化继续进行,并 获得了具有良好亚基选择性特征的有效 β5i 抑制剂54 (IC 50 = 8.463 nM)。化合物54还对 TNF-α 和 IL-6 的释放、NF-κB 的转录活性以及 TGF-β1 诱导的成纤维细胞增殖、活化和胶原蛋白合成产生显着影响。值得注意的是,当在博莱霉素诱导的 IPF 小鼠模型中以 30 mg/kg 给药时,化合物54显示出与临床药物尼达尼布相当的抗纤维化作用。结果表明,选择性抑制免疫蛋白酶体可能是治疗IPF的有效方法。
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(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐