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4‘-(1H-1,2,4-三唑基)苯酚 | 68337-15-5

中文名称
4‘-(1H-1,2,4-三唑基)苯酚
中文别名
4-(1,2,4-三唑基)苯酚;4-(1,2,4-三唑-1-基)苯酚
英文名称
4-(1,2,4-triazol-1-yl)phenol
英文别名
4-(1-H-1,2,4-triazol-1-yl)phenol;4-(1H-1,2,4-Triazol-1-yl)phenol
4‘-(1H-1,2,4-三唑基)苯酚化学式
CAS
68337-15-5
化学式
C8H7N3O
mdl
MFCD00003096
分子量
161.163
InChiKey
ZOPIBCDDKMAEII-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:
    254-257 °C
  • 沸点:
    287.45°C (rough estimate)
  • 密度:
    1.2558 (rough estimate)
  • 溶解度:
    DMSO(微溶)、甲醇(微溶、超声处理)
  • 稳定性/保质期:
    远离氧化物。

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    50.9
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xi
  • 安全说明:
    S24/25
  • 危险类别码:
    R36/37/38
  • 海关编码:
    2933990090
  • WGK Germany:
    3
  • 储存条件:
    存放在密封容器内,并置于阴凉、干燥处。存储地点须远离氧化剂。

SDS

SDS:bd3e757bcfc6e67948dabb6e4ae70825
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Name: 4 -(1H-1 2 4-Triazol-1-yl)phenol 98% Material Safety Data Sheet
Synonym: None
CAS: 68337-15-5
Section 1 - Chemical Product MSDS Name:4 -(1H-1 2 4-Triazol-1-yl)phenol 98% Material Safety Data Sheet
Synonym:None

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
68337-15-5 4'-(1H-1,2,4-Triazol-1-yl)phenol 98 269-845-2
Hazard Symbols: None Listed.
Risk Phrases: None Listed.

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Not available.
Potential Health Effects
Eye:
Causes eye irritation. May cause chemical conjunctivitis.
Skin:
Causes skin irritation.
Ingestion:
May cause gastrointestinal irritation with nausea, vomiting and diarrhea.
Inhalation:
Causes respiratory tract irritation. Can produce delayed pulmonary edema.
Chronic:
Effects may be delayed.

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.
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. Do NOT use mouth-to-mouth resuscitation.
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. 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. Avoid generating dusty conditions. Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Minimize dust generation and accumulation. Avoid contact with eyes, skin, and clothing. Avoid ingestion and inhalation. Use with adequate ventilation.
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# 68337-15-5: 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: Powder
Color: beige brown
Odor: none reported
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 254.00 - 257.00 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: C8H7N3O
Molecular Weight: 161.16

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable at room temperature in closed containers under normal storage and handling conditions.
Conditions to Avoid:
Incompatible materials, excess heat, strong oxidants.
Incompatibilities with Other Materials:
Strong oxidizing agents.
Hazardous Decomposition Products:
Nitrogen oxides, carbon monoxide, irritating and toxic fumes and gases, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 68337-15-5 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
4'-(1H-1,2,4-Triazol-1-yl)phenol - 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# 68337-15-5: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 68337-15-5 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 68337-15-5 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:
    4‘-(1H-1,2,4-三唑基)苯酚 在 sodium hydride 、 octachlorocyclotetraphosphazene 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 反应 171.0h, 以41%的产率得到oktakis{1-oxy-[4-(1,2,4-triazol-1-yl)]phenyl}cyclotetraphosphazene
    参考文献:
    名称:
    唑取代的环状和聚合磷腈的合成及质子电导率
    摘要:
    在本文中,我们描述了吡咯取代的环状和聚合的磷腈的合成,表征和质子传导性。通过元素分析,FT-IR,1 H,13 C和31 P NMR光谱对所有环状化合物HTCP,OTCP和聚合物PVTP进行了全面表征。用TGA&DSC研究了新合成的化合物的热性能,并在选定温度下通过阻抗光谱法测量了无水质子传导性。发现,在150℃下对掺杂有三氟甲烷磺酸的PVTP获得了0.043Scm -1的最大质子电导率,而没有分解。已获得环状衍生物HTCP作为P中的三斜晶 − 1个空间群,两个不对称单元中的水分子。X射线结构表征结果支持质子转移已通过Grotthuss机理得以保证。
    DOI:
    10.1016/j.polymer.2013.03.016
  • 作为产物:
    描述:
    1-(4-甲氧基苯基)-1H-1,2,4-三唑氢溴酸 作用下, 以 丙酮 为溶剂, 以5.5 parts (74%)的产率得到4‘-(1H-1,2,4-三唑基)苯酚
    参考文献:
    名称:
    Heterocyclic derivatives of 1-(1,3-dioxolan-2-ylmethyl)-1H-imidazoles
    摘要:
    1-(1,3-二氧戊环-2-基甲基)-1H-咪唑的杂环衍生物,作为抗真菌和抗菌剂有效。
    公开号:
    US04160841A1
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文献信息

  • [EN] TRICYCLIC PYRAZOLE KINASE INHIBITORS<br/>[FR] INHIBITEURS DE KINASES A BASE DE TYRAZOLES TRICYCLIQUES
    申请人:ABBOTT LAB
    公开号:WO2005095387A1
    公开(公告)日:2005-10-13
    Compounds of the present invention are useful for inhibiting protein tyrosine kinases. Also disclosed are methods of making the compounds, compositions containing the compounds, and methods of treatment using the compounds.
    本发明的化合物对抑制蛋白酪氨酸激酶具有用处。还公开了制备这些化合物的方法、含有这些化合物的组合物以及使用这些化合物进行治疗的方法。
  • Sulfamates as antiglaucoma agents
    申请人:A. H. Robins Company, Incorporated
    公开号:US05192785A1
    公开(公告)日:1993-03-09
    Sulfamate esters of the formula (HO).sub.p --A--[OSO.sub.2 NR.sup.1 R.sup.2 ].sub.z where A is aryloxyalkyl, p is the number of unreacted hydroxy groups present on the alkyl moiety and may be zero, z is the number of --OS(O).sub.2 NR.sup.1 R.sup.2 groups attached to carbons of the alkyl moiety and is always at least one; R.sup.1 and R.sup.2 are selected from hydrogen, loweralkyl, carboxy, and the like are useful in treating glaucoma.
    Sulfamate酯的化学式为(HO).sub.p --A--[OSO.sub.2 NR.sup.1 R.sup.2 ].sub.z,其中A为芳基氧烷基,p为烷基部分上存在的未反应羟基的数量,可以为零,z为连接到烷基部分碳上的--OS(O).sub.2 NR.sup.1 R.sup.2基团的数量,始终至少为一;R.sup.1和R.sup.2从氢、低烷基、羧基等中选择,在治疗青光眼方面是有用的。
  • Aryl and aryloxyalkyl sulfamate esters useful as anticonvulsants
    申请人:A. H. Robins Co., Inc.
    公开号:US05025031A1
    公开(公告)日:1991-06-18
    Herein disclosed is a method of treating convulsions with a pharmaceutical composition containing a compound of the formula: (HO).sub.p --A--[OSO.sub.2 NR.sup.1 R.sup.2 ].sub.z where A is an aryl, arylalkyl, or aryloxyalkyl group and is substituted on 1 or more carbon atoms with a sulfamate group (--OSO.sub.2 NR.sup.1 R.sup.2) wherein R.sup.1 and R.sup.2, same or different, are hydrogen or loweralkyl wherein p is 0 or 1 and is the number of untreated hydroxyl groups and z is 1 or 2 and is the number of --OS(O.sub.2)NR.sup.1 R.sup.2 groups. Aryl is selected from phenyl, substituted phenyl, pyridinyl, naphthyl, quinolinyl, and the like. Phenyl substituents are selected from hydrogen, halo, hydroxy, phenyl, phenoxy, benzoyl, loweralkyl, loweralkoxy, carboxy, amino, loweralkylamino, diloweralkylamino, acetamido, cyano, nitro, loweralkoxycarboyl, aminosulfonyl, imidazolyl, triazolyl, and the like. Novel compounds not previously disclosed are also described.
    以下披露了一种使用含有化合物的药物组合物来治疗惊厥的方法:(HO).sub.p --A--[OSO.sub.2 NR.sup.1 R.sup.2 ].sub.z,其中A是芳基、芳基烷基或芳氧烷基基团,并在1个或多个碳原子上用磺酰胺基团(--OSO.sub.2 NR.sup.1 R.sup.2)取代,其中R.sup.1和R.sup.2,相同或不同,是氢或较低烷基,其中p为0或1,是未处理的羟基团的数量,z为1或2,是--OS(O.sub.2)NR.sup.1 R.sup.2基团的数量。芳基选自苯基、取代苯基、吡啶基、萘基、喹啉基等。苯基取代基选自氢、卤素、羟基、苯基、苯氧基、苯甲酰基、较低烷基、较低烷氧基、羧基、氨基、较低烷基氨基、二较低烷基氨基、乙酰胺基、氰基、硝基、较低烷氧羰基、氨基磺酰基、咪唑基、三唑基等。还描述了以前未披露的新化合物。
  • Compounds having one or more aminosulfaonyloxy radicals useful as
    申请人:A. H. Robins Company, Incorporated
    公开号:US05194446A1
    公开(公告)日:1993-03-16
    Methods of treating chronic arthritis and osteoporosis which utilize both known and novel compounds which would fall under the general formula: (HO)p--A--[--OS(O).sub.2 NR.sup.1 R.sup.2 ].sub.z wherein A encompasses a wide range of values including but not limited to aryl, loweralkyl, cycloalkyl, and carbohydrates including sucrose and fructose; p is equal to the number of unreacted hydroxy groups contained on the molecule and may be zero; z is the number of --OS(O).sub.2 NR.sup.1 R.sup.2 groups and is always at least one; R.sup.1 and R.sup.2 are selected from hydrogen, loweralkyl, carboxy and the like; a novel process for preparing the compounds is provided wherein an appropriate sulfamic acid aryl ester is reacted with a hydroxy substituted A radical which may or may not contain thereon protected carboxyl, amino or hydroxy substituents, in an aprotic solvent containing a tertiary amine base. Pharmaceutical compositions for the treatment of chronic arthritis and osteoporosis are also provided.
    治疗慢性关节炎和骨质疏松症的方法利用已知和新颖的化合物,这些化合物可归入一般公式:(HO)p--A--[--OS(O).sub.2 NR.sup.1 R.sup.2 ].sub.z,其中A包括一系列值,包括但不限于芳基、较低烷基、环烷基和碳水化合物,包括蔗糖和果糖;p等于分子中未反应的羟基数,可以为零;z是--OS(O).sub.2 NR.sup.1 R.sup.2基团的数量,始终至少为一;R.sup.1和R.sup.2从氢、较低烷基、羧基等中选择;提供了一种制备这些化合物的新方法,其中适当的磺酸酯与含有保护羧基、氨基或羟基取代基的羟基取代的A基团在含有三级胺碱的无水溶剂中反应。还提供了用于治疗慢性关节炎和骨质疏松症的药物组合物。
  • CYCLOHEXANE ANALOGUES AS GPR119 AGONISTS
    申请人:Kang Sang Uk
    公开号:US20120053180A1
    公开(公告)日:2012-03-01
    This invention relates to a series of substituted cyclohexane containing analogues which are agonists of GPR119 intended to treat metabolic diseases mediated by GPR119 including Type I & II diabetes mellitus. Diabetes mellitus is an ever-increasing threat to human health causing various complications (blindness, kidney failure, neuropathy, heart attack, stroke, etc.). Recently it was found that activation of GPR119 which is highly expressed in pancreatic beta cells causes glucose dependent insulin secretion and GLP-1 release. Many pharmaceuticals are currently developing GPR119 agonists and herein we disclose alternative GPR119 agonists. Our invention describes GPR119 agonists having structural Formula (I), pharmaceutically acceptable salt or solvate of Formula (I), isomer or prodrug of Formula (I), and combination therapy of Formula (I) with other anti-diabetic drugs like DPP-IV inhibitors and/or insulin sensitizers.
    这项发明涉及一系列含有替代基的环己烷类似物,这些类似物是 GPR119 激动剂,旨在治疗由 GPR119 介导的代谢性疾病,包括I型和II型糖尿病。糖尿病是对人类健康构成日益增加的威胁,导致各种并发症(失明、肾衰竭、神经病变、心脏病发作、中风等)。最近发现,激活在胰岛素β细胞中高表达的 GPR119 会导致葡萄糖依赖性胰岛素分泌和 GLP-1 释放。许多制药公司目前正在开发 GPR119 激动剂,我们在此披露了替代的 GPR119 激动剂。我们的发明描述了具有结构式(I)的 GPR119 激动剂,结构式(I)的药学上可接受的盐或溶剂,结构式(I)的异构体或前药,以及结构式(I)与其他抗糖尿病药物(如 DPP-IV 抑制剂和/或胰岛素增敏剂)的联合治疗。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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