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4-(苯磺酰基)噻吩-2-磺酰氯 | 160233-28-3

中文名称
4-(苯磺酰基)噻吩-2-磺酰氯
中文别名
4-苯基噻酚-2,4-二磺酰氯;4-(苯基磺酰(基))硫代苯-2-磺酰氯
英文名称
4-benzene-sulfonylthiophene-2-sulfonyl chloride
英文别名
4-(phenylsulfonyl)thiophene-2-sulfonylchloride;4-benzenesulfonylthiophene-2-sulphonyl chloride;4-benzenesulfonylthiophene-2-sulfonyl chloride;4-(Benzenesulfonyl)thiophene-2-sulfonyl chloride
4-(苯磺酰基)噻吩-2-磺酰氯化学式
CAS
160233-28-3
化学式
C10H7ClO4S3
mdl
MFCD00052138
分子量
322.814
InChiKey
QTFQOMVQDFBUDL-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:
    101 °C
  • 沸点:
    519.7±35.0 °C(Predicted)
  • 密度:
    1.582±0.06 g/cm3(Predicted)
  • 稳定性/保质期:
    避热、防火焰、防光

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    18
  • 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:
    113
  • 氢给体数:
    0
  • 氢受体数:
    5

安全信息

  • 危险等级:
    8
  • 危险品标志:
    C
  • 安全说明:
    S26,S36/37/39,S45
  • 危险类别码:
    R34
  • 海关编码:
    2934999090
  • 包装等级:
    II
  • 危险类别:
    8
  • 危险品运输编号:
    3261

SDS

SDS:42aaef7a3cfcb0376d8bafcce3e09948
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Name: 4-Phenylthiophene-2 4-disulfonyl 97% Material Safety Data Sheet
Synonym:
CAS: 160233-28-3
Section 1 - Chemical Product MSDS Name:4-Phenylthiophene-2 4-disulfonyl 97% Material Safety Data Sheet
Synonym:

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
160233-28-3 4-Phenylthiophene-2,4-disulfonyl 97% unlisted
Hazard Symbols: C
Risk Phrases: 34

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Causes burns.Moisture sensitive.
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:
Vacuum or sweep up material and place into a suitable disposal 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. Do not use with metal spatula or other metal items.
Storage:
Store in a cool, dry place. Store in a tightly closed container.
Corrosives area. Do not store in metal containers. Store under nitrogen.

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# 160233-28-3: 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: off-white
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 101 - 103 deg C
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature: Not available.
Solubility in water:
Specific Gravity/Density:
Molecular Formula: C10H7ClO4S3
Molecular Weight: 323

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Not available.
Conditions to Avoid:
Incompatible materials, metals, exposure to moist air or water.
Incompatibilities with Other Materials:
Strong oxidizing agents, bases, reducing agents, alcohols, amines, metals.
Hazardous Decomposition Products:
Hydrogen chloride, chlorine, carbon monoxide, oxides of sulfur, carbon dioxide.
Hazardous Polymerization: Has not been reported.

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 160233-28-3 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
4-Phenylthiophene-2,4-disulfonyl - 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, ACIDIC, ORGANIC, N.O.S.*
Hazard Class: 8
UN Number: 3261
Packing Group: III
IMO
Shipping Name: CORROSIVE SOLID, ACIDIC, ORGANIC, N.O.S.
Hazard Class: 8
UN Number: 3261
Packing Group: III
RID/ADR
Shipping Name: CORROSIVE SOLID, ACIDIC, ORGANIC, N.O.S.
Hazard Class: 8
UN Number: 3261
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# 160233-28-3: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 160233-28-3 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 160233-28-3 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

  • 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:
    参考文献:
    名称:
    取代的磺酰基-N-羟基胍衍生物作为潜在的抗肿瘤剂的合成及细胞毒性评估。
    摘要:
    以铅化合物LY-181984为基础,设计合成了一系列磺酰基-N-羟基胍衍生物,作为潜在的抗癌药进行细胞毒性评价。用羟基胍代替前导化合物的脲基部分提供了稳定的细胞毒剂。磺酰基-N-羟基胍衍生物的构象,例如N-(4-氯苯基)-N'-[(苯并[2,1,3]噻二唑-4-基)磺酰基] -N“-羟基胍(4g),使用HMBC NMR,理论计算和X射线晶体学研究表明,这两个芳环堆叠在一起,并评估了这些衍生物对5种人类肿瘤细胞系的体外细胞毒性,包括HepG2,TSGH 8302,COLO 205,KB和MOLT -4。衍生化合物对人肿瘤细胞系的细胞毒活性等于或大于先导化合物。N-(4-氯苯基)-N'-[[3,5-二氯-4-(4-硝基苯氧基)苯基]磺酰基]-N“-羟基胍(4n)和N-(4-氯苯基)-N'- [[3,5-二氯-4-(2-氯-4-硝基苯氧基)苯基]磺酰基] -N”-羟基胍(4o)对实体瘤细胞系表现
    DOI:
    10.1021/jm9607818
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文献信息

  • Biphenylsulfonamides and derivatives thereof that modulate the activity of endothelin
    申请人:——
    公开号:US20020095041A1
    公开(公告)日:2002-07-18
    Biphenylsulfonamides and methods for modulating or altering the activity of the endothelin family of peptides are provided. In particular, bicyclic or tricyclic carbon or heterocyclic ring biphenylsulfonamides and methods using these sulfonamides for inhibiting the binding of an endothelin peptide to an endothelin receptor by contacting the receptor with the sulfonamide are provided. Methods for treating endothelin-mediated disorders by administering effective amounts of one or more of these sulfonamides or prodrugs thereof that inhibit or increase the activity of endothelin are also provided.
    提供了二苯基磺胺类化合物和调节或改变内皮素家族肽活性的方法。具体包括使用双环或三环碳或杂环环二苯基磺胺类化合物的方法,通过将该磺胺类化合物与内皮素受体接触来抑制内皮素肽与内皮素受体的结合。还提供了通过给予有效剂量的这些磺胺类化合物或其前药来治疗内皮素介导的疾病的方法,这些化合物能够抑制或增加内皮素的活性。
  • Convenient preparation of aryl ether derivatives using a sequence of functionalized polymers
    作者:Mike E. Lizarzaburu、Stephen J. Shuttleworth
    DOI:10.1016/s0040-4039(03)01117-1
    日期:2003.6
    A four-step synthesis to aryl ether derivatives, three of which utilize polymer-supported reagents, has been developed. Supported triphenylphosphine was successfully utilized in two distinct synthetic processes in the first step, whilst supported base and ionic and covalent scavengers were employed to complete the synthesis and purification of the target compounds.
    已开发出四步合成芳基醚衍生物的方法,其中三步使用聚合物负载的试剂。在第一步中,成功地将负载的三苯膦用于两个不同的合成过程中,同时使用负载的碱和离子和共价清除剂来完成目标化合物的合成和纯化。
  • Targeting quinolone- and aminocoumarin-resistant bacteria with new gyramide analogs that inhibit DNA gyrase
    作者:Katherine A. Hurley、Thiago M. A. Santos、Molly R. Fensterwald、Madhusudan Rajendran、Jared T. Moore、Edward I. Balmond、Brice J. Blahnik、Katherine C. Faulkner、Marie H. Foss、Victoria A. Heinrich、Matthew G. Lammers、Lucas C. Moore、Gregory D. Reynolds、Galen P. Shearn-Nance、Brian A. Stearns、Zi W. Yao、Jared T. Shaw、Douglas B. Weibel
    DOI:10.1039/c7md00012j
    日期:——
    potent inhibitors of DNA gyrase and are active against clinical strains of Gram-negative bacteria (Escherichia coli, Shigella flexneri, and Salmonella enterica; 3 of 10 wild-type strains tested) and Gram-positive bacteria (Bacillus spp., Enterococcus spp., Staphylococcus spp., and Streptococcus spp.; all 9 of the wild-type strains tested). E. coli strains resistant to the DNA gyrase inhibitors ciprofloxacin
    细菌DNA促旋酶是一种必不可少的II型拓扑异构酶,可使细胞克服复制,转录,重组和修复过程中遇到的拓扑障碍。该酶在细菌中无处不在,代表了抗菌治疗的重要临床目标。在本文中,我们从183个衍生物库中报告了三种激动人心的新型回旋酰胺类似物的表征,它们是DNA回旋酶的有效抑制剂,对革兰氏阴性菌(大肠杆菌,志贺氏志贺氏菌和肠炎沙门氏菌;测试的10种野生型菌株中有3种)和革兰氏阳性菌(芽孢杆菌,肠球菌,葡萄球菌spp。,and Streptococcus spp .; 所有9种野生型菌株都进行了测试)。对DNA促旋酶抑制剂环丙沙星和新霉素具有抗性的大肠杆菌菌株对这些新的乙二酰胺具有极小的交叉抗性。体外研究表明,新的类似物可有效抑制DNA促旋酶的DNA超螺旋活性(IC 50值为47–170 nM),但不会改变酶的ATPase活性。尽管赋予细菌细胞对这些新的回旋酰胺抗性的突变会映射到编码DNA回旋酶亚基的基
  • N-aryl thienyl-, furyl-, and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin
    申请人:Texas Biotechnology Corp.
    公开号:US06342610B2
    公开(公告)日:2002-01-29
    Thienyl-, furyl- and pyrrolyl-sulfonamides and methods for modulating or altering the activity of the endothelin family of peptides are provided. In particular, N-(isoxazolyl)thienylsulfonamides, N-(isoxazolyl)furylsulfonamides and N-(isoxazolyl)pyrrolylsulfonamides and methods using these sulfonamides for inhibiting the binding of an endothelin peptide to an endothelin receptor by contacting the receptor with the sulfonamide are provided. Methods for treating endothelin-mediated disorders by administering effective amounts of one or more of these sulfonamides or prodrugs thereof that inhibit or increase the activity of endothelin are also provided.
    提供了噻吩基、呋喃基和吡咯基磺酰胺以及用于调节或改变内皮素肽家族活性的方法。特别是,提供了N-(异恶唑基)噻吩磺酰胺、N-(异恶唑基)呋喃磺酰胺和N-(异恶唑基)吡咯磺酰胺以及使用这些磺酰胺通过将受体与磺酰胺接触来抑制内皮素肽与内皮素受体结合的方法。还提供了通过施用有效量的一个或多个这些磺酰胺或其前药来治疗内皮素介导的疾病的方法,这些磺酰胺或其前药抑制或增加内皮素的活性。
  • 4-aryloxindoles
    申请人:Hoffman-La Roche Inc.
    公开号:US06307056B1
    公开(公告)日:2001-10-23
    Disclosed are 4-aryloxindoles that inhibit or modulate protein kinases, in particular JNK protein kinases. These compounds and their pharmaceutically acceptable salts, and prodrugs of said compounds, are useful as anti-inflammatory agents, particularly useful in the treatment of rheumatoid arthritis. Also disclosed are pharmaceutical compositions containing the foregoing compounds, as well as methods for the treatment and/or control of inflammation, particularly in the treatment or control of rheumatoid arthritis, using said compounds.
    披露的是4-元氧杂吲哚类化合物,这些化合物可以抑制或调节蛋白激酶,特别是JNK蛋白激酶。这些化合物及其药用可接受的盐,以及这些化合物的前药,作为抗炎剂特别有用,尤其是在治疗类风湿性关节炎方面。还披露了包含上述化合物的药物组合物,以及使用这些化合物治疗和/或控制炎症的方法,特别是在治疗或控制类风湿性关节炎方面。
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同类化合物

(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