1-正-丁基-4-碘苯 | 20651-67-6

• 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: 1-正-丁基-4-碘苯
• 中文别名: 1-正丁基-4-碘苯；4-正丁基碘苯
• 英文名称: 4-butyliodobenzene
• 英文别名: 1-butyl-4-iodobenzene；4-n-butyliodobenzene；1-n-butyl-4-iodobenzene；p-(n-butyl)iodobenzene；1-iodo-4-butylbenzene
• CAS: 20651-67-6
• 化学式: C₁₀H₁₃I
• 分子量: 260.118
• InChiKey: XILRUONFYBUYIE-UHFFFAOYSA-N

物化性质

• 沸点：
  80-82°C 0,5mm
• 密度：
  1,462 g/cm3
• 闪点：
  80-82°C/0.5mm
• 稳定性/保质期：
  如果按照规格使用和储存，则不会分解，请避免接触光线及氧化物。

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  11
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

安全信息

• 危险品标志：
  Xi
• 安全说明：
  S26,S37/39
• 危险类别码：
  R36/37/38
• 海关编码：
  2903999090
• 危险性防范说明：
  P261,P301+P312,P302+P352,P304+P340,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H335
• 储存条件：
  保持贮藏器密封，并将其放入一个紧密封装的容器中。应储存在阴凉、干燥的地方。

SDS

Name:	1-Butyl-4-iodobenzene Material Safety Data Sheet
Synonym:
CAS:	20651-67-6

Section 1 - Chemical Product MSDS Name:1-Butyl-4-iodobenzene Material Safety Data Sheet
Synonym:

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Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS

CAS#	Chemical Name	content	EINECS#
20651-67-6	1-butyl-4-iodobenzene	97	unlisted

Hazard Symbols: None Listed.
Risk Phrases: None Listed.

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Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Not available.
Potential Health Effects
The toxicological properties of this material have not been investigated. Use appropriate procedures to prevent opportunities for direct contact with the skin or eyes and to prevent inhalation.

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Section 4 - FIRST AID MEASURES
Eyes: Not available.
Skin:
Not available.
Ingestion:
Not available.
Inhalation:
Not available.
Notes to Physician:

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Section 5 - FIRE FIGHTING MEASURES
General Information:
Not available.
Extinguishing Media:
Not available.

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Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Not available.

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Section 7 - HANDLING and STORAGE
Handling:
Not available.
Storage:
Not available.

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Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Exposure Limits CAS# 20651-67-6: Personal Protective Equipment Eyes: Not available.
Skin:
Not available.
Clothing:
Not available.
Respirators:
Not available.

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Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Liquid
Color: colorless - pale yellow
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: 85 - 87 deg C @0.05mmHg
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: C11H12O
Molecular Weight: 160

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Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Not available.
Conditions to Avoid:
Not available.
Incompatibilities with Other Materials:
Not available.
Hazardous Decomposition Products:
Not available.
Hazardous Polymerization: Has not been reported

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Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 20651-67-6 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
1-butyl-4-iodobenzene - Not listed by ACGIH, IARC, or NTP.

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Section 12 - ECOLOGICAL INFORMATION

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Section 13 - DISPOSAL CONSIDERATIONS
Dispose of in a manner consistent with federal, state, and local regulations.

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Section 14 - TRANSPORT INFORMATION

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

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Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: Not available.
Risk Phrases:
Safety Phrases:
WGK (Water Danger/Protection)
CAS# 20651-67-6: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 20651-67-6 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 20651-67-6 is not listed on the TSCA inventory.
It is for research and development use only.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  1-正-丁基-4-碘苯 在 C₁₂H₂₂CuN₂⁽¹⁺⁾*CF₃O₃S^(1-) 、 silver fluoride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 22.0h， 以74%的产率得到1-丁基-4-氟苯
  参考文献：
  名称：

  [EN] FLUORINATION OF ARYL COMPOUNDS
  [FR] FLUORATION DE COMPOSÉS ARYLE

  摘要：

  本发明提供了组合物和使用这些组合物的方法，用于氟化含有可被氟离子取代的离去基的芳基前体。这些组合物包括金属离子源、氟离子源和化合物，该化合物是芳基氟化物的芳基前体，并且具有可被氟离子取代的离去基。本发明的示例方法利用这些组合物和方法制备芳基氟化物化合物。在一个示例实施例中，氟离子源是18F的源。

  公开号：

  WO2013188554A1
• 作为产物：
  描述：

  丁苯 在 碘 、 碘酸 、 溶剂黄146 作用下， 生成 1-正-丁基-4-碘苯
  参考文献：
  名称：

  Boedtker, Bulletin de la Societe Chimique de France, 1929, vol. <4> 45, p. 648

  摘要：

  DOI：

文献信息

• Visible-light-promoted N-centered radical generation for remote heteroaryl migration
  作者：Chengkou Liu、Chen Cai、Chengcheng Yuan、Qiang Jiang、Zheng Fang、Kai Guo

  DOI：10.1039/d0ob01594f

  日期：——

  An efficient visible-light-mediated organocatalyzed N–H heteroarylation was accomplished via remote heteroaryl ipso-migration.

  通过远程杂芳基ipso-迁移实现了一种高效的可见光介导的有机催化N–H杂芳基化反应。

• Discovery of an Acrylic Acid Based Tetrahydroisoquinoline as an Orally Bioavailable Selective Estrogen Receptor Degrader for ERα+ Breast Cancer
  作者：Heather E. Burks、Tinya Abrams、Christina A. Kirby、Jason Baird、Alexander Fekete、Lawrence G. Hamann、Sunkyu Kim、Franco Lombardo、Alice Loo、Danuta Lubicka、Kaitlin Macchi、Donald P. McDonnell、Yuji Mishina、John D. Norris、Jill Nunez、Chitra Saran、Yingchuan Sun、Noel M. Thomsen、Chunrong Wang、Jianling Wang、Stefan Peukert

  DOI：10.1021/acs.jmedchem.6b01468

  日期：2017.4.13

  as a potent ERα antagonist and selective estrogen receptor degrader (SERD), exhibiting good oral bioavailability, antitumor efficacy, and SERD activity in vivo. We outline the discovery and chemical optimization of the THIQ scaffold leading to THIQ 40 and showcase the racemization of the scaffold, pharmacokinetic studies in preclinical species, and the in vivo efficacy of THIQ 40 in a MCF-7 human breast

  四氢异喹啉40已被确定为有效的ERα拮抗剂和选择性雌激素受体降解剂（SERD），在体内具有良好的口服生物利用度，抗肿瘤功效和SERD活性。我们概述了导致THIQ 40的THIQ支架的发现和化学优化，并展示了支架的消旋作用，临床前物种的药代动力学研究以及THIQ 40在MCF-7人乳腺癌异种移植模型中的体内功效。
• Palladium-Catalyzed Decarboxylative<i>sp</i>-<i>sp</i>²Cross-Coupling Reactions of Aryl and Vinyl Halides and Triflates with α,β-Ynoic Acids using Silver Oxide
  作者：Hyunseok Kim、Phil Ho Lee

  DOI：10.1002/adsc.200900502

  日期：2009.11

  Palladium-catalyzed decarboxylative sp-sp2 cross-coupling reactions of aryl and vinyl halides and triflates with α,β-ynoic acids using silver oxide have been developed. A variety of α,β-ynoic acids were readily decarboxylated in the presence of silver oxide and then, generated in situ, silver acetylides were coupled with electrophiles in the presence of a palladium(0) catalyst under neutral conditions

  已经开发了使用氧化银的芳族卤化物和乙烯基卤化物以及三氟甲磺酸与钯，α-炔酸的钯催化的脱羧sp-sp 2交叉偶联反应。多种α，β炔酸在氧化银的存在下，容易地脱羧，然后，生成的原位，银乙炔化物加上在中性条件下在钯（0）催化剂的存在下亲电子，产生对称或不对称的二芳基乙炔，芳基烷基乙炔和芳基乙烯基乙炔，收率良好至优异。
• Synthesis and properties of thieno[2,3-d:5,4-d’]bisthiazoles and their oxidized derivatives: Thionyl chloride as a sulfurative ring-fusing reagent towards thiophene-based ring-fused heteroaromatic compounds
  作者：Ryuta Wada、Shigesaki Kaga、Yasuhiro Kawai、Kimitaka Futamura、Toshiaki Murai、Fumitoshi Shibahara

  DOI：10.1016/j.tet.2021.131978

  日期：2021.3

  A new route to thiophene-ring-fused compounds with thionyl chloride as a sulfur source was developed. Use of an excess amount thionyl chloride directly gave the corresponding thiophene-ring-fused compound via further reduction of generated thiophene-S-oxide with excess thionyl chloride in some cases. One-pot reduction with tributylphosphine also gave thiophene-ring-fused compounds in good yields, and

  开发了一种以亚硫酰氯为硫源的噻吩环稠合化合物的新途径。在某些情况下，通过用过量的亚硫酰氯进一步还原生成的噻吩-S-氧化物，使用过量的亚硫酰氯可直接得到相应的噻吩-环稠合的化合物。用三丁基膦一锅还原也可得到高产率的噻吩环稠合化合物，用NaClO·5H 2 O氧化可得到S-二氧化物。另外，获得的噻唑-噻吩环稠合化合物之一显示出一些出乎意料的机械致变色行为。
• A general method for the formation of diaryl selenides using copper(I) catalysts
  作者：Rattan K Gujadhur、D Venkataraman

  DOI：10.1016/s0040-4039(02)02480-2

  日期：2003.1

  We report a mild, palladium-free synthetic protocol for the cross coupling reaction of aryl iodides and phenyl selenol using 10 mol% CuI/neocuproine, NaOt-Bu or K2CO3 as base, in toluene, at 110°C. Using this protocol, we show that a variety of diaryl selenides can be synthesized in good yields from commercially available aryl iodides.

  我们报告了一种温和的，不含钯的合成方案，用于在110°C的甲苯中，使用10 mol％CuI /新磷腈，NaO t -Bu或K 2 CO 3作为碱，对芳基碘化物和苯基硒酚进行交叉偶联反应。使用该协议，我们表明可以从商业上可获得的芳基碘化物以高收率合成多种二芳基硒化物。