CAS: 82461-14-1; 2,4-Dimethyl-4-Phenyltetrahydrofuran
该化合物是一种有机化合物,其独特结构包括一个四氢呋喃环,由两个甲基组和一个苯基组替代,该化合物是五人组成的四氢呋喃类别的成员,是五人组成的环状醚,其分子结构有助于其特性,包括其在有机溶剂中的溶性以及有机合成和溶剂中的潜在应用;该苯基组的存在增强了其芳香特性,可能影响其再活动以及与其他化学物种的相互作用;此外,二甲基替代物可影响其沸点和稳定性;尽管熔点,沸点和密度等具体的物理特性可能各不相同,但一般预期该化合物会表现出类似有机化合物典型的中等波动性和再活动性;在处理和储存时,应参考安全数据,如任何化学物质,以确保采取适当的预防措施.
- 英文名称2,4-Dimethyl-4-Phenyltetrahydrofuran
- 中文名称2,4-二甲基-4-苯基四氢呋喃
- IUPAC名称2,4-dimethyl-4-phenyltetrahydrofuran
- 其它别名2,4-Dimethyl-4-Phenyl Tetrahydrofuran; Rhubafuran; 2,4-Dimethyl-4-Phenyloxolane; Tetrahydro-2,4-Dimethyl-4-Phenylfuran; Furan, Tetrahydro-2,4-Dimethyl-4-Phenyl-; Tetrahydro-2,4-Dimethyl-4-Phenyl-Fura
- CAS编号82461-14-1
- MFCD编号:MFCD00169859
- EINECS号:279-967-8
- FDA UNII编号:85JUZ61OL5
- 分子式:C12H16O分子量:176.26
- 产品CID: 1815360
- 产品分类有机原料→分子砌块→芳环类化合物→苯类化合物
相似化合物
2059912-17-1 2059911-06-5 2059917-46-1物理性质
- 沸点248.7 °C at 760 mmHg
- 闪点99.9 °C
- 密度0.966 g/cm3
- PSA:9.23
- LogP:2.7531
- 折射率1.502
- 蒸汽压2.5Pa at 20°C
- 溶解性650mg/L at 20°C
- 外观形态无色至淡黄色液体
- 储存条件Dry, dark and at 0 -4 C for short term (days to weeks) or -20 C for long term(months to years).
- 产品应用该化合物是以其潜在的抗氧化剂和防炎特性而闻名的胡巴布自然产生的化合物,在皮肤保护产品中应用该化合物有助于保护皮肤免受氧化性压力和环境损害,而鲁巴弗兰则涉及清除自由基质和减少炎症,这可以支持皮肤健康,有助于抗衰竭效应,其温和而有效的特性使它成为针对敏感或衰老皮肤的配方中有价值的成分.
欧盟法规
REACH注册ECHA物质C&L通报REACH预注册上下游产品
2-methyl-2-phenylpent-4-en-1-ol 2-Phenylpropanal 2-methyl-2-phenyl-pentenal N-phenyl-2-methyl-2-phenyl-4-pentenylideneamine合成工艺路线路线简述
- 93-53-8 = 82461-14-1
反应条件:1.1 Catalysts: Trifluoroacetic Acid,Tetrakis(Triphenylphosphine)Palladium Solvents: Benzene1.2 Reagents: Hydrochloric Acid Solvents: Water2.1 Reagents: Lithium Aluminum Hydride Solvents: Diethyl Ether3.1 Reagents: Mercuric Acetate Solvents: Tetrahydrofuran,Water3.2 Reagents: Sodium Hydroxide,Sodium Borohydride Solvents: Water
标题:Palladium(0)-Catalyzed Rearrangement Of N-Allyl Enamines. Synthesis Of δ,ε-Unsaturated Imines And γ,δ-Unsaturated Carbonyl Compounds
作者:Murahashi,Shunichi; Et Al
参考文献:Journal Of Organic Chemistry 日期:1988 卷标:53(19) 页码:4489-95]
82461-15-2 = 82461-14-1
反应条件:1.1 Reagents: Mercuric Acetate Solvents: Tetrahydrofuran,Water1.2 Reagents: Sodium Hydroxide,Sodium Borohydride Solvents: Water
标题:Palladium(0)-Catalyzed Rearrangement Of N-Allyl Enamines. Synthesis Of δ,ε-Unsaturated Imines And γ,δ-Unsaturated Carbonyl Compounds
作者:Murahashi,Shunichi; Et Al
参考文献:Journal Of Organic Chemistry 日期:1988 卷标:53(19) 页码:4489-95]
24401-39-6 = 82461-14-1
反应条件:1.1 Reagents: Lithium Aluminum Hydride Solvents: Diethyl Ether2.1 Reagents: Mercuric Acetate Solvents: Tetrahydrofuran,Water2.2 Reagents: Sodium Hydroxide,Sodium Borohydride Solvents: Water
标题:Palladium(0)-Catalyzed Rearrangement Of N-Allyl Enamines. Synthesis Of δ,ε-Unsaturated Imines And γ,δ-Unsaturated Carbonyl Compounds
作者:Murahashi,Shunichi; Et Al
参考文献:Journal Of Organic Chemistry 日期:1988 卷标:53(19) 页码:4489-95]
93-53-8 = 82461-14-1
反应条件:1.1 Catalysts: Trifluoroacetic Acid,Tetrakis(Triphenylphosphine)Palladium Solvents: Benzene1.2 Reagents: Hydrochloric Acid Solvents: Water2.1 Reagents: Lithium Aluminum Hydride Solvents: Diethyl Ether3.1 Reagents: Mercuric Acetate Solvents: Tetrahydrofuran,Water3.2 Reagents: Sodium Hydroxide,Sodium Borohydride Solvents: Water
标题:Palladium(0)-Catalyzed Rearrangement Of N-Allyl Enamines. Synthesis Of δ,ε-Unsaturated Imines And γ,δ-Unsaturated Carbonyl Compounds
作者:Murahashi,Shunichi; Et Al
参考文献:Journal Of Organic Chemistry 日期:1988 卷标:53(19) 页码:4489-95]
115913-92-3 = 82461-14-1
反应条件:1.1 Catalysts: Trifluoroacetic Acid,Tetrakis(Triphenylphosphine)Palladium Solvents: Benzene1.2 Reagents: Hydrochloric Acid Solvents: Water2.1 Reagents: Lithium Aluminum Hydride Solvents: Diethyl Ether3.1 Reagents: Mercuric Acetate Solvents: Tetrahydrofuran,Water3.2 Reagents: Sodium Hydroxide,Sodium Borohydride Solvents: Water
标题:Palladium(0)-Catalyzed Rearrangement Of N-Allyl Enamines. Synthesis Of δ,ε-Unsaturated Imines And γ,δ-Unsaturated Carbonyl Compounds
作者:Murahashi,Shunichi; Et Al
参考文献:Journal Of Organic Chemistry 日期:1988 卷标:53(19) 页码:4489-95]
93-53-8 + 589-09-3 = 82461-14-1
反应条件:1.1 Catalysts: Trifluoroacetic Acid,Tetrakis(Triphenylphosphine)Palladium Solvents: Benzene1.2 Reagents: Hydrochloric Acid Solvents: Water2.1 Reagents: Lithium Aluminum Hydride Solvents: Diethyl Ether3.1 Reagents: Mercuric Acetate Solvents: Tetrahydrofuran,Water3.2 Reagents: Sodium Hydroxide,Sodium Borohydride Solvents: Water
标题:Palladium(0)-Catalyzed Rearrangement Of N-Allyl Enamines. Synthesis Of δ,ε-Unsaturated Imines And γ,δ-Unsaturated Carbonyl Compounds
作者:Murahashi,Shunichi; Et Al
参考文献:Journal Of Organic Chemistry 日期:1988 卷标:53(19) 页码:4489-95
📜2-甲基-2-苯基戊-4-烯醛置于sodium Hydroxide,Sodium Tetrahydroborate,Lithium Aluminium Tetrahydride,Mercury(II) Diacetate体系中,用 乙醚 作为反应溶剂,化学反应 15.0H,反应生成 2,4-二甲基-4-苯基四氢呋喃
参考文献:Palladium(0)-Catalyzed Rearrangement Of N-Allyl Enamines. Synthesis Of .Delta.,.Epsilon.-Unsaturated Imines And .Gamma.,.Delta.-Unsaturated Carbonyl Compounds
标题:Palladium(0)-Catalyzed Rearrangement Of N-Allyl Enamines. Synthesis Of .Delta.,.Epsilon.-Unsaturated Imines And .Gamma.,.Delta.-Unsaturated Carbonyl Compounds
摘要:
DOI:10.1021/jo00254A013
海关参考信息
- 2902600000-乙苯
2902700000-异丙基苯
2905122000-异丙醇
2909110000-乙醚 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:US-2021198229-A1
优先权日:2018-03-08
标 题 :Fragrance and flavor materials from 1-(2-hydroxy-4-methylcyclohexyl)-ethanone
发明人：DICKERSON THALIA S; LOMBARDO LOUIS J; LANKIN MICHAEL E
权利人:TAKASAGO PERFUMERY CO LTD
摘要:The present disclosure is directed to 1-(2-hydroxy-4-methycyclohexyl)-ethanone derivatives having unique and desired flavor and/or fragrance characteristics, as well as the synthesis and application of the derivatives. The compounds of the present disclosure can be employed alone or incorporated as fragrance or flavor ingredients to modify or enhance already existing fragrance compositions, solvents, media, and the like.
专利号:US-2020407301-A1
优先权日:2018-03-08
标 题:Fragrance and flavor materials derived from 1-(4-methylcyclohex-1-en-1-yl)ethan-1-one
发明人：BLANDINO MAUREEN; LANKIN MICHAEL E; LOMBARDO LOUIS J
权利人:TAKASAGO PERFUMERY CO LTD
摘要:The present disclosure is directed to 1-(4-methyl cyclohex-1-en-1-yl)ethan-1-one derivatives having unique and desired flavor and/or fragrance characteristics, as well as the synthesis and application of the derivatives. The compounds of the present disclosure can be employed alone or incorporated as fragrance or flavor ingredients to modify or enhance already existing fragrance compositions, solvents, media, and the like.
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