4-benzylsulfanylbenzoic acid | 22855-95-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-benzylsulfanylbenzoic acid
• 英文别名: 4-(benzylthio)benzoic acid；p-(benzylthio)benzoic acid；4-benzylthiobenzoic acid；4-benzylsulfanyl-benzoic acid；4-Benzylmercapto-benzoesaeure；4-(Benzylsulfanyl)benzoic acid
• CAS: 22855-95-4
• 化学式: C₁₄H₁₂O₂S
• mdl: MFCD06804476
• 分子量: 244.314
• InChiKey: BIGZCUUCDAVUIJ-UHFFFAOYSA-N

物化性质

• 熔点：
  189-190 °C
• 沸点：
  423.5±38.0 °C(Predicted)
• 密度：
  1.27±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  17
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.071
• 拓扑面积：
  62.6
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 海关编码：
  2930909090

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 4-(Benzylsulfanyl)benzoic acid
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-(Benzylsulfanyl)benzoic acid
CAS number: 22855-95-4

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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.
Storage: Store in closed vessels.

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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
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C14 H12 O2 S
Molecular weight: 244.3

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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, 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-benzylsulfanylbenzoic acid 在 氯化亚砜 、 双氧水 、 三乙胺 作用下， 以 四氢呋喃 、 溶剂黄146 为溶剂， 反应 4.17h， 生成 1-benzyl-4-<2-amino>ethyl>piperidine
  参考文献：
  名称：

  新型哌啶衍生物。1-苄基-4- [2-（N-苯甲酰基氨基）乙基]哌啶衍生物的合成和抗乙酰胆碱酯酶活性。

  摘要：

  合成了一系列的1-苄基-4- [2-（N-苯甲酰基氨基）乙基]哌啶衍生物，并评估了其抗乙酰胆碱酯酶（anti-AChE）的活性。用对位上的大体积部分取代苯甲酰胺导致活性显着增加。在苯甲酰胺的氮原子上引入烷基或苯基大大增强了活性。哌啶氮原子的基本质量似乎在活性增加中起重要作用，因为N-苯甲酰基哌啶衍生物几乎没有活性。我们发现1-苄基-4- [2-（N- [4'-（苄基磺酰基）苯甲酰基] -N-甲基氨基]乙基]哌啶盐酸盐（21）（IC50 = 0.56 nM）是最有效的抑制剂之一化合物21对AChE的亲和力比对BuChE的亲和力大18,000倍，剂量为3 mg / kg时，21在大鼠的脑涡和海马中产生了乙酰胆碱（ACh）含量的显着显着增加。选择化合物21作为抗痴呆剂进行高级开发。

  DOI：

  10.1021/jm00169a008
• 作为产物：
  描述：

  4,4’-二硫二苯甲酸 在 氨 、 sodium 作用下， 生成 4-benzylsulfanylbenzoic acid
  参考文献：
  名称：

  292.氨基酸系列的抑菌作用。第二部分 丙氨酸衍生物的进一步研究

  摘要：

  DOI：

  10.1039/jr9490001374

文献信息

• Sulfide synthesis through copper-catalyzed C–S bond formation under biomolecule-compatible conditions
  作者：Yonghong Zhang、Yiming Li、Xiaomei Zhang、Xuefeng Jiang

  DOI：10.1039/c4cc08367a

  日期：——

  We report here an efficient, mild and biomolecule-compatible method for constructing C–S bonds.

  我们在这里报告了一种高效、温和且生物分子兼容的构建C-S键的方法。
• Hydrazide and alkoxyamide angiogenesis inhibitors
  申请人：——

  公开号：US20020002152A1

  公开（公告）日：2002-01-03

  Compounds having the formula 1 are methionine aminopeptidase type 2 (MetAP2) inhibitors and are useful for inhibiting angiogenesis. Also disclosed are MetAP2-inhibiting compositions and methods of inhibiting angiogenesis in a mammal.

  具有以下化学式的化合物是蛋氨酸氨肽酶2型（MetAP2）抑制剂，对抑制血管生成有用。还公开了抑制MetAP2的组合物和在哺乳动物中抑制血管生成的方法。
• A Facile One-Pot Synthesis of Alkyl Aryl Sulfides from Aryl Bromides
  作者：Jungyeob Ham、Inho Yang、Heonjoong Kang

  DOI：10.1021/jo049758h

  日期：2004.4.1

  one-pot synthetic method for the formation of alkyl aryl sulfides from various alkyl halides and lithium aryl thiolates that are prepared in situ by direct halogen−lithium exchange is reported. In particular, the method overcomes many of the problems encountered in previous reports; it is very quick, catalyst-free, and does not involve use of unstable aryl thiols.

  报道了一种方便的一锅合成方法，该方法由各种烷基卤和芳基硫醇锂通过直接卤素-锂交换原位制备形成烷基芳基硫醚。尤其是，该方法克服了先前报告中遇到的许多问题。它非常快速，无催化剂，并且不涉及使用不稳定的芳基硫醇。
• Mercaptobenzoic acid-palladium(0) complexes as active catalysts for S-benzylation with benzylic alcohols via (η³-benzyl)palladium(<scp>ii</scp>) cations in water
  作者：Hidemasa Hikawa、Isao Azumaya

  DOI：10.1039/c4ob00688g

  日期：——

  of the respective substituents. From the slope, negative rho values are obtained, suggesting that there is a build-up of positive charge in the transition state. Water plays an important role in the catalytic system for sp(3) C-O bond activation and stabilization of the activated Pd(II) cation species. The catalytic system can be performed using only 2.5 mol% Pd2(dba)3 without the phosphine ligand or

  巯基苯甲酸-钯（0）配合物通过水中的（eta（3）-苄基）钯（II）阳离子对苄基醇进行S-苄基化反应显示出高催化活性。值得注意的是，这些钯（0）配合物可以在形成活性（eta（3）-苄基）钯（II）阳离子配合物，然后进行S-苄基化过程中发挥重要作用。Hammett对各种取代醇进行S-苄基化反应的速率常数的研究表明，log（kX / kH）与各个取代基的sigma（+）值之间具有良好的相关性。从斜率可以得到负rho值，这表明在过渡态中会积聚正电荷。水在sp（3）CO键活化和活化Pd（II）阳离子物种的稳定化催化体系中起着重要作用。催化系统只能使用2进行。
• Palladium-catalyzed S-benzylation of unprotected mercaptobenzoic acid with benzyl alcohols in water
  作者：Hidemasa Hikawa、Yuusaku Yokoyama

  DOI：10.1039/c2ob25091h

  日期：——

  Palladium-catalyzed S-benzylation of unprotected mercaptobenzoic acids with benzyl alcohols gave only S-benzylated mercaptobenzoic acids in good yields. Water may play an important role for the smooth generation of the (η3-benzyl)palladium species by activation of the hydroxyl group of the benzyl alcohol.

  钯催化下，用苄醇对未保护的硫代苯甲酸进行S-苄基化反应仅生成S-苄基化硫代苯甲酸，且产率良好。水可能在通过激活苄醇的羟基生成(η3-苄基)钯物种的过程中特别重要。