3-丁氧基-2-环己烯-1-酮 | 16493-04-2

• 物质功能分类: 有机原料 - 酮类化合物
• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 3-丁氧基-2-环己烯-1-酮
• 英文名称: 3-butanoxycyclohex-2-en-1-one
• 英文别名: 3-butoxycyclohex-2-en-1-one；3-butoxy-2-cyclohexenone；3-butoxy-cyclohex-2-enone；3-Butoxy-cyclohex-2-enon；3-n-butoxy-2-cyclohexen-1-one
• CAS: 16493-04-2
• 化学式: C₁₀H₁₆O₂
• mdl: MFCD00190682
• 分子量: 168.236
• InChiKey: HQFGJBVERCJECK-UHFFFAOYSA-N

物化性质

• 沸点：
  280.6±29.0 °C(Predicted)
• 密度：
  0.97±0.1 g/cm3(Predicted)
• LogP：
  1.96

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  12
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 危险品标志：
  Xi
• 危险类别码：
  R20/21/22
• 海关编码：
  2914509090
• 安全说明：
  S36/37

SDS

Name:	3-Butoxycyclohex-2-en-1-one 97% Material Safety Data Sheet
Synonym:
CAS:	16493-04-2

Section 1 - Chemical Product MSDS Name:3-Butoxycyclohex-2-en-1-one 97% Material Safety Data Sheet
Synonym:

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Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS

CAS#	Chemical Name	content	EINECS#
16493-04-2	3-Butoxycyclohex-2-en-1-one	97%	240-557-9

Hazard Symbols: XN
Risk Phrases: 20/21/22

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Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Harmful by inhalation, in contact with skin and if swallowed.
Potential Health Effects
Eye:
May cause eye irritation.
Skin:
May cause skin irritation. Harmful if absorbed through the skin.
Ingestion:
Harmful if swallowed. May cause irritation of the digestive tract.
Inhalation:
Harmful if inhaled. May cause respiratory tract irritation.
Chronic:
Not available.

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Section 4 - FIRST AID MEASURES
Eyes: 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.
Ingestion:
Get medical aid. Wash mouth out with 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.
Notes to Physician:

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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 water spray, dry chemical, carbon dioxide, or chemical foam.

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Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Absorb spill with inert material (e.g. vermiculite, sand or earth), then place in suitable container.

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Section 7 - HANDLING and STORAGE
Handling:
Avoid breathing dust, vapor, mist, or gas. Avoid contact with skin and eyes.
Storage:
Store in a cool, dry place. Store in a tightly closed container.

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Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Use adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 16493-04-2: 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.

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Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Liquid
Color: yellow
Odor: Not available.
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: C10H16O2
Molecular Weight: 168

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Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Not available.
Conditions to Avoid:
Incompatible materials.
Incompatibilities with Other Materials:
Strong oxidizing agents, reducing agents.
Hazardous Decomposition Products:
Carbon monoxide, carbon dioxide.
Hazardous Polymerization: Has not been reported

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Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 16493-04-2 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
3-Butoxycyclohex-2-en-1-one - 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
Shipping Name: TOXIC LIQUID, ORGANIC, N.O.S.*
Hazard Class: 6.1
UN Number: 2810
Packing Group: III
IMO
Shipping Name: TOXIC LIQUID, ORGANIC, N.O.S.
Hazard Class: 6.1
UN Number: 2810
Packing Group: III
RID/ADR
Shipping Name: TOXIC LIQUID, ORGANIC, N.O.S.
Hazard Class: 6.1
UN Number: 2810
Packing group: III

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Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: XN
Risk Phrases:
R 20/21/22 Harmful by inhalation, in contact with
skin and if swallowed.
Safety Phrases:
S 36/37 Wear suitable protective clothing and
gloves.
WGK (Water Danger/Protection)
CAS# 16493-04-2: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 16493-04-2 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 16493-04-2 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：

  3-丁氧基-2-环己烯-1-酮 在 水 作用下， 20.0~80.0 ℃ 、330.01 kPa 条件下， 反应 0.31h， 生成 1,3-环己二酮
  参考文献：
  名称：

  连续流动条件下葡萄酒酯的快速和多克合成：葡萄酒酯的醚交换和逆反应

  摘要：

  在廉价的Amberlyst-15催化剂存在下，用醇类开发了一种从1,3-二酮合成乙烯基酯及其在连续流下逆反应的环境友好方法。这种方法学具有高度的选择性，对一系列环状的1,3-二羰基化合物具有通用性，在无溶剂和无金属的条件下，该文库可提供线性至烷基化和芳基化的乙烯基酯库，收率高至极佳。此外，在长达40小时的连续流中进行的长时间实验得到了8.0 g的乙烯基酯，其周转数（TON）= 28.6，周转频率（TOF）= 0.715 h –1使用Amberlyst-15作为催化剂。此外，已经以高收率实现了乙烯基酯与各种醇的连续流动顺序的醚交换。可逆地，使用环境友好的水作为溶剂，使用Amberlyst-15作为催化剂，在连续流过程中将该乙烯基酯脱保护或水解为酮。

  DOI：

  10.1021/acs.oprd.9b00067
• 作为产物：
  描述：

  3-乙氧基-2-环己烯-1-酮 在 Amberlyst-15 作用下， 80.0 ℃ 、330.01 kPa 条件下， 生成 3-丁氧基-2-环己烯-1-酮
  参考文献：
  名称：

  连续流动条件下葡萄酒酯的快速和多克合成：葡萄酒酯的醚交换和逆反应

  摘要：

  在廉价的Amberlyst-15催化剂存在下，用醇类开发了一种从1,3-二酮合成乙烯基酯及其在连续流下逆反应的环境友好方法。这种方法学具有高度的选择性，对一系列环状的1,3-二羰基化合物具有通用性，在无溶剂和无金属的条件下，该文库可提供线性至烷基化和芳基化的乙烯基酯库，收率高至极佳。此外，在长达40小时的连续流中进行的长时间实验得到了8.0 g的乙烯基酯，其周转数（TON）= 28.6，周转频率（TOF）= 0.715 h –1使用Amberlyst-15作为催化剂。此外，已经以高收率实现了乙烯基酯与各种醇的连续流动顺序的醚交换。可逆地，使用环境友好的水作为溶剂，使用Amberlyst-15作为催化剂，在连续流过程中将该乙烯基酯脱保护或水解为酮。

  DOI：

  10.1021/acs.oprd.9b00067

文献信息

• Synthesis of 9E- and 9Z-Locked Retinoic Acid Analogs As Ligands for RAR and RXR.
  作者：Yuko KATSUTA、Yukiko AOYAMA、Hisa OSONE、Akimori WADA、Shimami UCHIYAMA、Takuya KITAMOTO、Shoichi MASUSHIGE、Shigeaki KATO、Masayoshi ITO

  DOI：10.1248/cpb.42.2659

  日期：——

  New retinoic acid (RA) analogs 9E-locked-RA 3 and 9Z-locked-RA 4 were synthesized from dithiane 6 and beta-cyclocitral 13, respectively. Both analogs behaved as agonistic ligands for a mixture of retinoic acid receptor (RAR) and retinoid X receptor (RXR).

  新的视黄酸（RA）类似物9E-锁合的RA 3和9Z-锁合的RA 4分别由二噻吩6和β-环柠檬酸酯13合成。两种类似物均充当视黄酸受体（RAR）和类维生素X受体（RXR）混合物的激动配体。
• CATALYST FOR ASYMMETRIC HYDROGENATION
  申请人：MAEDA Hironori

  公开号：US20100324338A1

  公开（公告）日：2010-12-23

  This invention aims at providing a catalyst for producing an optically active aldehyde or an optically active ketone, which is an optically active carbonyl compound, by carrying out selective asymmetric hydrogenation of an α,β-unsaturated carbonyl compound, particularly a catalyst which is insoluble in a reaction mixture for obtaining optically active citronellal which is useful as a flavor or fragrance, by carrying out selective asymmetric hydrogenation of citral, geranial or neral; and a method for producing a corresponding optically active carbonyl compound. The invention relates to a catalyst for asymmetric hydrogenation of an α,β-unsaturated carbonyl compound, which comprises a powder of at least one metal selected from metals belonging to Group 8 to Group 10 of the Periodic Table, or a metal-supported substance in which at least one metal selected from metals belonging to Group 8 to Group 10 of the Periodic Table is supported on a support, an optically active cyclic nitrogen-containing compound and an acid.

  这项发明旨在通过对α，β-不饱和羰基化合物进行选择性不对称加氢，特别是通过对柠檬醛、香叶醛或柠檬醛进行选择性不对称加氢，从而提供用作香料或香精的有用的光学活性香茅醛的催化剂，该香茅醛是一种光学活性羰基化合物；以及生产相应的光学活性羰基化合物的方法。该发明涉及一种用于不对称加氢α，β-不饱和羰基化合物的催化剂，其包括来自周期表第8至第10族金属中至少一种金属的粉末，或者至少一种来自周期表第8至第10族金属的金属负载物质，该金属负载在一种支撑物上，还包括光学活性的含氮环化合物和酸。
• Iron(III) Tosylate in the Preparation of Dimethyl and Diethyl Acetals from Ketones and <font> <b>β</b> </font>-Keto Enol Ethers from Cyclic <font> <b>β</b> </font>-Diketones
  作者：Horacio Mansilla、María M. Afonso

  DOI：10.1080/00397910802219361

  日期：2008.7.24

  Abstract An efficient method for conversion of ketones to their corresponding dimethyl and diethyl acetals and of cyclic β-diketones into β-keto enol ethers using Fe(OTs)3 as a catalyst is described.

  摘要 描述了一种使用 Fe(OTs)3 作为催化剂将酮转化为相应的二甲基和二乙基缩醛以及将环状 β-二酮转化为 β-酮烯醇醚的有效方法。
• Solvent Free Rapid Synthesis of 3-Alkoxycyclohex-2-en-1-one from 1,3-Cyclohexanedione Promoted by Indium(III) Chloride/Silica Gel
  作者：R. Murugan、R. Kamakshi、Boreddy S. R. Reddy

  DOI：10.1071/ch04249

  日期：——

  A convenient and environmentally friendly method for the synthesis of 3-alkoxycyclohex-2-en-1-one 1 from cyclohexane-1,3-dione on the surface of silica gel impregnated with indium(iii) chloride under microwave irradiation without any solvent has been reported.

  据报道，一种简便、环保的方法可在微波辐照下，不使用任何溶剂，在氯化铟（iii）浸渍过的硅胶表面，从环己烷-1,3-二酮合成 3-烷氧基环己-2-烯-1-酮 1。
• Cerium(IV) Ammonium Nitrate-catalyzed Synthesis of β-Keto Enol Ethers from Cyclic β-Diketones and Their Deprotection
  作者：Biplab Banerjee、Samir Kumar Mandal、Subhas Chandra Roy

  DOI：10.1246/cl.2006.16

  日期：2006.1

  A mild and efficient method for etherification of cyclic β-diketones with alcohols has been developed using a catalytic amount of cerium(IV) ammonium nitrate at room temperature to afford the corre...

  使用催化量的硝酸铈（IV）铵在室温下开发了一种温和有效的环β-二酮与醇醚化的方法，以提供正确的...