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1-ó4-(溴甲基)苯-1H-1,2,4-三唑 | 58419-69-5

中文名称
1-ó4-(溴甲基)苯-1H-1,2,4-三唑
中文别名
1-[4-(溴甲基)苯基]-1H-1,2,4-三氮唑;1-[4-(溴甲基)苯基]-1H-1,2,4-三唑
英文名称
1-[4-(bromomethyl)phenyl]-1H-1,2,4-triazole
英文别名
1-(4-(bromomethyl)phenyl)-1H-1,2,4-triazole;1-[4-(bromomethyl)phenyl]-1,2,4-triazole
1-ó4-(溴甲基)苯-1H-1,2,4-三唑化学式
CAS
58419-69-5
化学式
C9H8BrN3
mdl
——
分子量
238.087
InChiKey
NOUAEJFAVOHNSY-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:
    280 °C
  • 沸点:
    366.2±44.0 °C(Predicted)
  • 密度:
    1.55±0.1 g/cm3 (20 ºC 760 Torr)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    30.7
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 安全说明:
    S26,S36/37/39,S45
  • 危险类别码:
    R34
  • 海关编码:
    2933990090

SDS

SDS:a75261c6443d714e655ce7cf2de59c1c
查看
Name: 1-[4-(Bromomethyl)phenyl]-1h-1 2 4-triazole 97% Material Safety Data Sheet
Synonym:
CAS: 58419-69-5
Section 1 - Chemical Product MSDS Name:1-[4-(Bromomethyl)phenyl]-1h-1 2 4-triazole 97% Material Safety Data Sheet
Synonym:

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
58419-69-5 1-[4-(Bromomethyl)phenyl]-1H-1,2,4-tri 97% unlisted
Hazard Symbols: C
Risk Phrases: 34

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Causes burns.
Potential Health Effects
Eye:
Causes eye burns.
Skin:
Causes skin burns.
Ingestion:
Causes gastrointestinal tract burns.
Inhalation:
Causes chemical burns to the respiratory tract.
Chronic:
Not available.

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 immediately.
Skin:
Get medical aid immediately. Immediately flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes.
Ingestion:
Do not induce vomiting. Get medical aid immediately.
Inhalation:
Get medical aid immediately. Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen.
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 foam, dry chemical, or carbon dioxide.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Absorb spill with inert material (e.g. vermiculite, sand or earth), then place in suitable container.

Section 7 - HANDLING and STORAGE
Handling:
Do not breathe dust, vapor, mist, or gas. Do not get in eyes, on skin, or on clothing. Use only in a chemical fume hood.
Storage:
Store in a cool, dry place. Store in a tightly closed container.
Corrosives area.

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# 58419-69-5: Personal Protective Equipment Eyes: Not available.
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: white
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 280 - 285 deg C(decom)
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: C9H8BrN3
Molecular Weight: 238.09

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Not available.
Conditions to Avoid:
Incompatible materials.
Incompatibilities with Other Materials:
Strong oxidizing agents, amines.
Hazardous Decomposition Products:
Nitrogen oxides, carbon monoxide, carbon dioxide, hydrogen bromide, bromine.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 58419-69-5 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
1-[4-(Bromomethyl)phenyl]-1H-1,2,4-triazole - 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: CORROSIVE SOLID, N.O.S.*
Hazard Class: 8
UN Number: 1759
Packing Group: III
IMO
Shipping Name: CORROSIVE SOLID, N.O.S.
Hazard Class: 8
UN Number: 1759
Packing Group: III
RID/ADR
Shipping Name: CORROSIVE SOLID, N.O.S.
Hazard Class: 8
UN Number: 1759
Packing group: III

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: C
Risk Phrases:
R 34 Causes burns.
Safety Phrases:
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.
S 45 In case of accident or if you feel unwell, seek
medical advice immediately (show the label where
possible).
WGK (Water Danger/Protection)
CAS# 58419-69-5: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 58419-69-5 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 58419-69-5 is not listed on the TSCA inventory.
It is for research and development use only.


SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

  • 作为反应物:
    描述:
    1-ó4-(溴甲基)苯-1H-1,2,4-三唑环丙沙星potassium carbonate 作用下, 以 乙腈 为溶剂, 反应 117.08h, 生成 7-(4-(4-(1H-1,2,4-triazol-1-yl)benzyl)piperazin-1-yl)-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
    参考文献:
    名称:
    [EN] ANTIBIOTIC RESISTANCE BREAKERS
    [FR] AGENTS DE RUPTURE DE RÉSISTANCE AUX ANTIBIOTIQUES
    摘要:
    该发明涉及公式(A1)的抗生素化合物及其药学上可接受的盐、溶剂化合物、互变异构体和它们的组合,其中X和L是可选的连接物,RA或R1中的一个包括Ar1,其中Ar1是一种抗生素耐药性破坏基团,包括可选择取代的C6-10芳基,C7-13芳基烷基,C5-10杂芳基,C6-13杂芳基烷基,C5-10杂环烷基,C6-13杂环烷基,C3-10碳环烷基,C4-13碳环烷基,-C(=NR')-NR'R''或–CH2- CH=CH2基团;在将该化合物用于细菌感染后,该基团减少或预防外流。该发明还公开了包括公式(A1)化合物的药物组合物以及将这些化合物用作药物的用途,特别是用于治疗细菌感染,如耐药性细菌感染。
    公开号:
    WO2018220365A1
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文献信息

  • Sulfonamides
    申请人:Galley Guido
    公开号:US20060014945A1
    公开(公告)日:2006-01-19
    The invention relates to compounds of the general formula in which R 1 , R 2 , R3, R 4 , R 2′ , R3′, R 4′ , R 5 , and X is —CHR— are as defined in the specification. The invention also provides pharmaceutically acceptable acid addition salts, optically pure enantiomers, racemates and diastereomeric mixtures of such compounds. The invention further provides methods for the treatment of Alzheimer's disease or common cancers.
    该发明涉及一般式化合物,其中R1、R2、R3、R4、R2'、R3'、R4'、R5和X为规范中定义的—CHR—。该发明还提供药学上可接受的酸盐加合物,光学纯对映体,外消旋体和这类化合物的二对映异构体混合物。该发明还提供治疗阿尔茨海默病或常见癌症的方法。
  • A phase-switch purification approach for the expedient removal of tagged reagents and scavengers following their application in organic synthesis
    作者:Jason Siu、Ian R. Baxendale、Russell A. Lewthwaite、Steven V. Ley
    DOI:10.1039/b503778f
    日期:——
    In this paper we wish to report on a variety of expedient chemical transformations and purifications achieved via a generic ‘catch and release’ methodology, based on a synthetically inert bipyridyl chelating tag that can be selectively captured with a resin-bound copper(II) species. Utilising this approach we are able to derive many of the same benefits associated with both solid phase synthesis and supported reagent methods.
    本文旨在报道通过一种基于合成不活跃的双吡啶螯合标签的通用“捕获与释放”方法,实现的一系列便捷的化学转化和纯化。该方法可以选择性地利用树脂结合的铜(II)物种来捕获双吡啶螯合标签。采用这种方法,我们能够获得与固相合成和支持试剂法相关的许多相同益处。
  • [DE] IMIDAZOL-DERIVATE ALS TAFIA-INHIBITOREN<br/>[EN] IMIDAZOLE DERIVATIVES USED AS TAFIA INHIBITORS<br/>[FR] DERIVES D'IMIDAZOLE SERVANT D'INHIBITEURS DE TAFIA
    申请人:AVENTIS PHARMA GMBH
    公开号:WO2005105781A1
    公开(公告)日:2005-11-10
    Die Erfindung betrifft Verbindungen der Formel (I), die Inhibitoren von aktivierter Thrombin-aktivierbarer Fibrinolyse Inhibitor sind. Die Verbindungen der Formel I eignen sich zur Herstellung von Arzneimitteln zur Prophylaxe und Therapie von Erkrankungen, die mit Thrombosen, Embodien, Hyperkoagulabilität oder fibrotischen Veränderungen einhergehen.
    这项发明涉及公式(I)的连接物,其为激活的凝血酶激活纤溶抑制剂。公式I的连接物适用于制备用于预防和治疗与血栓形成、栓塞、高凝状态或纤维化变化相关的疾病的药物。
  • Identification of a Selective, Non-Prostanoid EP2 Receptor Agonist for the Treatment of Glaucoma: Omidenepag and its Prodrug Omidenepag Isopropyl
    作者:Ryo Iwamura、Masayuki Tanaka、Eiji Okanari、Tomoko Kirihara、Noriko Odani-Kawabata、Naveed Shams、Kenji Yoneda
    DOI:10.1021/acs.jmedchem.8b00808
    日期:2018.8.9
    receptor agonists are expected to be effective ocular hypotensive agents; however, it has been suggested that agonism to other EP receptor subtypes may lead to undesirable effects. Through medicinal chemistry efforts, we identified a scaffold bearing a (pyridin-2-ylamino)acetic acid moiety as a promising EP2-selective receptor agonist. (6-((4-(Pyrazol-1-yl)benzyl)(pyridin-3-ylsulfonyl)aminomethyl)pyri
    预期EP2受体激动剂是有效的降眼压药。然而,已经提出对其他EP受体亚型的激动作用可能导致不良作用。通过药物化学的努力,我们确定了带有(吡啶-2-基氨基)乙酸部分的支架是有前途的EP2选择性受体激动剂。(6-((4-(吡唑-1-基)苄基)(吡啶-3-基磺酰基)氨基甲基)吡啶-2-基氨基)乙酸13ax(omidenepag,OMD)对人EP2受体具有有效的选择性活性( h-EP2)。低剂量的奥米地帕异丙(OMDI)(一种13ax的前药)可降低正常眼压性猴子的眼内压(IOP)。OMDI被选为治疗青光眼的临床候选药物。
  • IMIDAZOLE DERIVATIVES USED AS TAFIA INHIBITORS
    申请人:Kallus Christopher
    公开号:US20070129341A1
    公开(公告)日:2007-06-07
    The present invention relates to compounds of formula (I) which are inhibitors of the activated thrombin-activatable fibrinolysis inhibitor. The compounds of formula (I) are suited for producing medicaments for the prevention and treatment of diseases accompanied by thromboses, embolisms, hypercoagulability or fibrotic changes.
    本发明涉及式(I)的化合物,这些化合物是活化凝血酶可激活纤溶抑制剂的抑制剂。式(I)的化合物适用于生产用于预防和治疗伴随有血栓形成、栓塞、高凝状态或纤维化变化的疾病的药物。
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