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(9ci)-1H-1,2,4-噻唑-1-丙醇 | 84497-70-1

中文名称
(9ci)-1H-1,2,4-噻唑-1-丙醇
中文别名
——
英文名称
1-(3-hydroxypropyl)-[1,2,4]-triazole
英文别名
3-(1,2,4-triazol-1-yl)propan-1-ol
(9ci)-1H-1,2,4-噻唑-1-丙醇化学式
CAS
84497-70-1
化学式
C5H9N3O
mdl
MFCD03727266
分子量
127.146
InChiKey
IFIXOVUEWNCJED-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

  • 沸点:
    310.3±44.0 °C(Predicted)
  • 密度:
    1.24±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.4
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    50.9
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933990090

SDS

SDS:d8ea525250d76477152675ba56585893
查看
Name: 3-[1H-(1 2 4-Triazolyl)]-Propanol Material Safety Data Sheet
Synonym: None known
CAS: 84497-70-1
Section 1 - Chemical Product MSDS Name:3-[1H-(1 2 4-Triazolyl)]-Propanol Material Safety Data Sheet
Synonym:None known

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
84497-70-1 3-[1H-(1,2,4-Triazoyl)]-Propanol ca 100 unlisted
Hazard Symbols: XI
Risk Phrases: 36/37/38

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Irritating to eyes, respiratory system and skin.The toxicological properties of this material have not been fully investigated.
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. The toxicological properties of this substance have not been fully investigated.
Inhalation:
Causes respiratory tract irritation. The toxicological properties of this substance have not been fully investigated. 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. Use water spray to keep fire-exposed containers cool. Vapors may be heavier than air. They can spread along the ground and collect in low or confined areas. Containers may explode when heated.
Extinguishing Media:
Use agent most appropriate to extinguish fire. Cool containers with flooding quantities of water until well after fire is out. 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:
Avoid runoff into storm sewers and ditches which lead to waterways.
Clean up spills immediately, observing precautions in the Protective Equipment section. Absorb spill using an absorbent, non-combustible material such as earth, sand, or vermiculite. Do not use combustible materials such as sawdust. Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. 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 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# 84497-70-1: 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: Liquid
Color: straw-colored - oily
Odor: aromatic odor
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: Not available.
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: C5H9N3O
Molecular Weight: 127.0825

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.
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# 84497-70-1 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
3-[1H-(1,2,4-Triazoyl)]-Propanol - Not listed by ACGIH, IARC, or NTP.

Section 12 - ECOLOGICAL INFORMATION


Section 13 - DISPOSAL CONSIDERATIONS
Products which are considered hazardous for supply are classified as Special Waste and the disposal of such chemicals is covered by regulations which may vary according to location. Contact a specialist disposal company or the local waste regulator for advice. Empty containers must be decontaminated before returning for recycling.

Section 14 - TRANSPORT INFORMATION

IATA
No information available.
IMO
No information available.
RID/ADR
No information available.

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: XI
Risk Phrases:
R 36/37/38 Irritating to eyes, respiratory system
and skin.
Safety Phrases:
S 26 In case of contact with eyes, rinse immediately
with plenty of water and seek medical advice.
S 36/39 Wear suitable protective clothing and
eye/face protection.
WGK (Water Danger/Protection)
CAS# 84497-70-1: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 84497-70-1 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 84497-70-1 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

反应信息

  • 作为反应物:
    描述:
    (9ci)-1H-1,2,4-噻唑-1-丙醇 、 4-(4-氯-2-氟苯基氨基)-7-羟基-6-甲氧基喹唑啉 在 三苯基膦偶氮二甲酸二乙酯盐酸 作用下, 以 二氯甲烷甲醇乙醚 为溶剂, 反应 3.0h, 以39%的产率得到4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(3-(1,2,4-triazol-1-yl)propoxy)quinazoline hydrochloride
    参考文献:
    名称:
    Chemical compounds
    摘要:
    该发明涉及以下结构的喹唑啉衍生物:[其中:Y1代表—O—、—S—、—CH2—、—SO—、—SO2—、—NR5CO—、—CONR6—、—SO2NR7—、—NR8SO2—或—NR9—(其中R5、R6、R8和R9分别独立代表氢、烷基或烷氧基烷基);R1代表氢、羟基、卤素、硝基、三氟甲基、氰基、烷基、烷氧基、烷硫基、氨基或烷基氨基。R2代表氢、羟基、卤素、烷基、烷氧基、三氟甲基、氰基、氨基或硝基;m为1到5的整数;R3代表羟基、卤素、烷基、烷氧基、烷酰氧基、三氟甲基、氰基、氨基或硝基;R4代表一个或含有一个可选择取代的吡啶酮、苯基或芳香杂环基团的基团]及其盐;其制备方法以及含有I式化合物或其药学上可接受的盐作为活性成分的药物组合物。I式化合物及其药学上可接受的盐抑制VEGF的作用,这在治疗包括癌症和类风湿关节炎在内的多种疾病状态中具有价值。
    公开号:
    US06362336B1
  • 作为产物:
    描述:
    ethyl 3-(1H-1,2,4-triazol-1-yl)propanoateLithium aluminium hydride水合甲醇甲醇 、 title product 作用下, 以 乙醚 为溶剂, 反应 60.0h, 生成 (9ci)-1H-1,2,4-噻唑-1-丙醇
    参考文献:
    名称:
    4-anilinoquinoline-3-carboxamides
    摘要:
    本发明涉及一种新型化合物(IA式),它们是JAK3激酶抑制剂,以及它们的制备方法和包含它们的药物组合物。
    公开号:
    US07037925B2
点击查看最新优质反应信息

文献信息

  • Substituted quinazolines
    申请人:Zeneca Limited
    公开号:US05962458A1
    公开(公告)日:1999-10-05
    The invention relates to quinazoline derivatives of the formula: ##STR1## \x9bwherein: Y.sup.1 represents --O--, --S--, --CH.sub.2 --, --SO--, --SO.sub.2 --, --NR.sup.5 CO--, --CONR.sup.6 -, --SO.sub.2 NR.sup.7 -, --NR.sup.8 SO.sub.2 -- or --NR.sup.9 - (wherein R.sup.5, R.sup.6, R.sup.7, R.sup.8 and R.sup.9 each independently represents hydrogen, alkyl or alkoxyalkyl); R.sup.1 represents hydrogen, hydroxy, halogeno, nitro, trifluoromethyl, cyano, alkyl, alkoxy, alkylthio, amino or alkylamino. R.sup.2 represents hydrogen, hydroxy, halogeno, alkyl, alkoxy, trifluoromethyl, cyano, amino or nitro; m is an integer from 1 to 5; R.sup.3 represents hydroxy, halogeno, alkyl, alkoxy, alkanoyloxy, trifluoromethyl, cyano, amino or nitro; R.sup.4 represents a group which is or which contains an optionally substituted pyridone, phenyl or aromatic heterocyclic group! and salts thereof; processes for their preparation and pharmaceutical compositions containing a compound of formula I or a pharmaceutically acceptable salt thereof as active ingredient. The compounds of formula I and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis.
    本发明涉及公式为:##STR1##的喹唑啉衍生物,其中:Y.sup.1代表--O--,--S--,--CH.sub.2--,--SO--,--SO.sub.2--,--NR.sup.5CO--,--CONR.sup.6-,--SO.sub.2NR.sup.7-,--NR.sup.8SO.sub.2--或--NR.sup.9-(其中R.sup.5,R.sup.6,R.sup.7,R.sup.8和R.sup.9分别独立地代表氢,烷基或烷氧基烷基);R.sup.1代表氢,羟基,卤代,硝基,三氟甲基,氰基,烷基,烷氧基,烷硫基,氨基或烷基氨基。R.sup.2代表氢,羟基,卤代,烷基,烷氧基,三氟甲基,氰基,氨基或硝基;m为1至5的整数;R.sup.3代表羟基,卤代,烷基,烷氧基,烷酰氧基,三氟甲基,氰基,氨基或硝基;R.sup.4代表一个含有或不含有可选取代的吡啶酮,苯基或芳香族杂环基的基团!及其盐;其制备过程和含有公式I化合物或其药学上可接受的盐作为活性成分的药物组合物。公式I化合物及其药学上可接受的盐能够抑制VEGF的作用,这种特性在治疗包括癌症和类风湿性关节炎在内的多种疾病状态中具有价值。
  • Quinazoline Derivatives as Angiogenesis Inhibitors
    申请人:Stokes Elaine S.E.
    公开号:US20120197027A1
    公开(公告)日:2012-08-02
    The invention relates to the use of compounds of formula (I) and salts thereof, in the manufacture of a medicament for use in the production of an antiangiogenic and/or vascular permeability reducing effect in warm-blooded animals, processes for the preparation of such compounds, pharmaceutical compositions containing a compound of formula I or a pharmaceutically acceptable salt thereof as active ingredient and compounds of formula I. The compounds of formula I and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis.
    该发明涉及使用式(I)的化合物及其盐,在制造用于在温血动物中产生抗血管生成和/或减少血管通透性效果的药物中的应用,制备这种化合物的方法,含有式I的化合物或其药学上可接受的盐作为活性成分的药物组合物以及式I的化合物。式(I)的化合物及其药学上可接受的盐抑制VEGF的效果,这是在治疗包括癌症和类风湿性关节炎在内的多种疾病状态中具有价值的特性。
  • Quinazoline derivatives as angiogenesis inhibitors
    申请人:Stokes Elaine S E
    公开号:US08492560B2
    公开(公告)日:2013-07-23
    The invention relates to the use of compounds of formula (I) and salts thereof, in the manufacture of a medicament for use in the production of an antiangiogenic and/or vascular permeability reducing effect in warm-blooded animals, processes for the preparation of such compounds, pharmaceutical compositions containing a compound of formula I or a pharmaceutically acceptable salt thereof as active ingredient and compounds of formula I. The compounds of formula I and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis.
    本发明涉及使用式(I)化合物及其盐在制造用于在温血动物体内产生抗血管生成和/或降低血管通透性效应的药物中的应用,制备这种化合物的过程,含有式(I)化合物或其药学上可接受的盐作为活性成分的制药组合物和式(I)化合物。式(I)化合物及其药学上可接受的盐抑制VEGF的效应,在治疗包括癌症和类风湿性关节炎在内的多种疾病状态中具有价值的特性。
  • Chemical compounds
    申请人:Zeneca Limited
    公开号:US06362336B1
    公开(公告)日:2002-03-26
    The invention relates to quinazoline derivatives of the formula: [wherein: Y1 represents —O—, —S—, —CH2—, —SO—, —SO2—, —NR5CO—, —CONR6—, —SO2NR7—, —NR8SO2— or —NR9— (wherein R5, R6, R8 and R9 each independently represents hydrogen, alkyl or alkoxyalkyl); R1 represents hydrogen, hydroxy, halogeno, nitro, trifluoromethyl, cyano, alkyl, alkoxy, alkylthio, amino or alkylamino. R2 represents hydrogen, hydroxy, halogeno, alkyl, alkoxy, trifluoromethyl, cyano, amino or nitro; m is an integer from 1 to 5; R3 represents hydroxy, halogeno, alkyl, alkoxy, alkanoyloxy, trifluoromethyl, cyano, amino or nitro; R4 represents a group which is or which contains an optionally substituted pyridone, phenyl or aromatic heterocyclic group] and salts thereof; processes for their preparation and pharmaceutical compositions containing a compound of formula I or a pharmaceutically acceptable salt thereof as active ingredient. The compounds of formula I and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis.
    该发明涉及以下结构的喹唑啉衍生物:[其中:Y1代表—O—、—S—、—CH2—、—SO—、—SO2—、—NR5CO—、—CONR6—、—SO2NR7—、—NR8SO2—或—NR9—(其中R5、R6、R8和R9分别独立代表氢、烷基或烷氧基烷基);R1代表氢、羟基、卤素、硝基、三氟甲基、氰基、烷基、烷氧基、烷硫基、氨基或烷基氨基。R2代表氢、羟基、卤素、烷基、烷氧基、三氟甲基、氰基、氨基或硝基;m为1到5的整数;R3代表羟基、卤素、烷基、烷氧基、烷酰氧基、三氟甲基、氰基、氨基或硝基;R4代表一个或含有一个可选择取代的吡啶酮、苯基或芳香杂环基团的基团]及其盐;其制备方法以及含有I式化合物或其药学上可接受的盐作为活性成分的药物组合物。I式化合物及其药学上可接受的盐抑制VEGF的作用,这在治疗包括癌症和类风湿关节炎在内的多种疾病状态中具有价值。
  • 4-anilinoquinoline-3-carboxamides
    申请人:AstraZeneca AB
    公开号:US07037925B2
    公开(公告)日:2006-05-02
    The present invention relates to novel compounds of formula (IA), which are JAK3 Kinase inhibitors, methods for their preparation and pharmaceutical compositions comprising them.
    本发明涉及一种新型化合物(IA式),它们是JAK3激酶抑制剂,以及它们的制备方法和包含它们的药物组合物。
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