4-(丁基磺酰基)苯胺 | 51770-72-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 4-(丁基磺酰基)苯胺
• 中文别名: 4-(丁烷-1-磺酰基)苯胺
• 英文名称: (4-Aminophenyl)-butyl-sulfon
• 英文别名: 4-aminophenyl butyl sulfone；4-butylsulfonylaminobenzene；4-(butane-1-sulfonyl)-aniline；4-Butylsulfon-anilin；Butyl-(4-amino-phenyl)-sulfon；4-(Butan-1-sulfonyl)-anilin；4-(Butylsulfonyl)aniline；4-butylsulfonylaniline
• CAS: 51770-72-0
• 化学式: C₁₀H₁₅NO₂S
• 分子量: 213.301
• InChiKey: HBNSCBAEYVWNNV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  68.5
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 海关编码：
  2921420090
• 危险性防范说明：
  P261,P264,P270,P271,P280,P301+P312+P330,P302+P352,P304+P340+P312,P305+P351+P338,P332+P313,P337+P313,P362,P403+P233,P405,P501
• 危险性描述：
  H302,H315,H319,H335
• 储存条件：
  室温

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 4-(Butane-1-sulfonyl)aniline
Synonyms:

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Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

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Section 3. Composition/information on ingredients.
Ingredient name: 4-(Butane-1-sulfonyl)aniline
CAS number: 51770-72-0

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Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

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Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

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Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

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Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels.
Storage:

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Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

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Section 9. Physical and chemical properties
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C10H15NO2S
Molecular weight: 213.3

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Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides, sulfur oxides.

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Section 11. Toxicological information
No data.

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Section 12. Ecological information
No data.

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Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

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Section 14. Transportation information
Non-harzardous for air and ground transportation.

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Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  4-(丁基磺酰基)苯胺 在 吡啶 、 盐酸 、 potassium carbonate 、 sodium nitrite 作用下， 以 二氯甲烷 、 水 、 丙酮 为溶剂， 生成 4-(8-acroyloxyoctyloxy)-4'-butylsulfonylazobenzene
  参考文献：
  名称：

  Photorefractive Effect of Liquid Crystalline Polymers Possessing Azobenzene Chromophores

  摘要：

  A series of liquid crystalline polymers possessing azobenzene chromophores were synthesized, and in each polymer the photorefractive effect of the isotropic phase was investigated. The photorefractive effect was evaluated by a four-wave mixing experiment. The diffraction efficiency of a side-chain liquid crystalline polymer possessing chiral moieties was measured and compared with that of a polymer possessing achiral chromophores. Chiral polymers exhibited unusual electric-field dependence on diffraction efficiency. The effects of liquid crystallinity and chiral substituents on photorefractivity are discussed.

  DOI：

  10.1080/10587250210541
• 作为产物：
  描述：

  对乙酰氨基苯亚磺酸 在 盐酸 作用下， 以 乙醇 、 水 为溶剂， 反应 28.0h， 生成 4-(丁基磺酰基)苯胺
  参考文献：
  名称：

  合成烷基芳基，环烷基和芳基-（4-氨基苯基）-磺化剂的方法

  摘要：

  某些烷基-，环烷基-和芳基-（4-氨基苯基）砜的合成

  DOI：

  10.1002/hlca.19830660407

文献信息

• Cardioselective aryloxy- and arylthio-hydroxypropyl piperazinyl acetanilides wich affect calcium entry
  申请人：SYNTEX (U.S.A.) INC.

  公开号：EP0126449A1

  公开（公告）日：1984-11-28

  Novel compounds of the general formula and the pharmaceutically acceptable esters and acid addition salts thereof, wherein: R1, R2, R3, R4, and R5 are each independently hydrogen, lower alkyl, lower alkoxy, cyano, trifluoromethyl, halo, lower alkylthio, lower alkyl sulfinyl, lower alkyl sulfonyl, N-optionally substituted alkylamido, except that when R1 is methyl, R4 is not methyl; or R2 and R3 together form -OCH2O-; R6, R7, R8, R9 and R10 are each independently hydrogen, lower acyl, aminocarbonyl-methyl, arylcyano, lower alkyl, lower alkoxy, trifluoromethyl, halo, lower alkylthio, lower alkyl sulfinyl, lower alkyl sulfonyl, di-lower alkyl amino; or R6 and R7 together form -CH = CH-CH = CH-; R7 and R8 together form -OCH2O -; R11 and R12 are each independently hydrogen or lower alkyl; and W is oxygen or sulfur. These cardioselective compounds have calcium entry blockade properties and therefore are useful in therapy in the treatment of cardiovascular diseases, including arrhythmias, variant and exercise induced angina and myocardial infarction.

  通式为 及其药学上可接受的酯和酸加成盐，其中 R1、R2、R3、R4 和 R5 各自独立地为氢、低级烷基、低级烷氧基、氰基、三氟甲基、卤代、低级烷硫基、低级烷基亚磺酰基、低级烷基磺酰基、N-可选取代的烷基氨基，但当 R1 为甲基时，R4 不是甲基；或 R2 和 R3 共同形成 -OCH2O-； R6、R7、R8、R9 和 R10 各自独立地为氢、低级酰基、氨基羰基甲基、芳基氰基、低级烷基、低级烷氧基、三氟甲基、卤代、低级烷硫基、低级烷基亚磺酰基、低级烷基磺酰基、二低级烷基氨基；或 R6 和 R7 共同形成 -CH = CH-CH = CH-； R7 和 R8 共同形成 -OCH2O -； R11 和 R12 各自独立地为氢或低级烷基；以及 W 是氧或硫。 这些心脏选择性化合物具有钙离子进入阻断特性，因此可用于治疗心血管疾病，包括心律失常、变异型和运动诱发的心绞痛和心肌梗塞。
• Some Phenylthiourea Derivatives and their Antituberculous Activity
  作者：L. Doub、L. M. Richardson、D. R. Herbst、M. L. Black、O. L. Stevenson、L. L. Bambas、G. P. Youmans、A. S. Youmans

  DOI：10.1021/ja01542a043

  日期：1958.5
• DE755395
  申请人：——

  公开号：——

  公开（公告）日：——
• Organic-Inorganic Hybrid Materials for Nonlinear Optics Applications
  作者：Kwang-Sup Lee、Tae-Dong Kim、Yu Hong Min、Choon Sup Yoon、Marek Samoc、Anna Samoc

  DOI：10.1080/10587250008025686

  日期：2000.12

  Three types of organic-inorganic hybrid materials were prepared by the sol-gel processable monomers derived from 3-isocyanatopropyltriethoxysilane with three different hydroxy-functionalized nonlinear optical chromophores. The measured values of NLO coefficient strongly depended on conditions such as poling temperature, poling time and heating rate. The hybrid films heated at 200 degreesC exhibited d(33) = 50-58 pm/V in Maker-fringe measurement. It was found that the thermal stabilities of the films were greatly enhanced as poling time increased and a poling temperature became higher. Also, we observed good waveguiding properties of the films at 810 nm and 1063 nm. The optical propagation losses of the films for TE mode were about 2 dB/cm at 810 nm and 0.5 dB/cm at 1064 nm.
• Jain; Iyer; Guha, Journal of the Indian Chemical Society, 1947, vol. 24, p. 220
  作者：Jain、Iyer、Guha

  DOI：——

  日期：——