CAS: 23283-97-8; (+)-Isomenthol

该化合物是源自月球的循环单体酒精,其特征是其性能,作为异族新醇的对应体之一,特别是(+)形式,具有薄膜芳香.该化合物在室内温度下一般是无色的,可粉黄黄色液体,在酒精和醚中溶解,但在水中则因其疏水特性而较少溶解.其分子结构具有环形特征,具有氢氧化物组,有助于其功能性.(+)-Isomenthol在香味和调味行业以及个人护理产品的配制中普遍使用,因为其香味和冷却感.此外,该化合物在制药和有机合成中作为土气建筑块具有潜在用途.其安全特征表明毒性低,适合各种消费品.

结构式图片

相似化合物

89-78-1 2216-52-6 2623-23-6

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号89-83-8 麝香草酚 | CAS号2216-51-5 (-)-薄荷醇 | CAS号2216-52-6 (+)-新薄荷醇 | CAS号1044169-05-2 (1R,2R,4R)-2-溴-... | CAS号1196-31-2 (+)-异薄荷酮 | CAS号500-00-5 para-3-menthene

合成工艺路线路线简述

    百里酚置于氢气,镍体系中,化学反应生成(+)-异薄荷醇
    参考文献:Brunel,Bulletin De La Societe Chimique De France,1905,Vol. <3> 33,P. 269,500
    标题:Brunel,Bulletin De La Societe Chimique De France,1905,Vol. <3> 33,P. 269,500

    海关参考信息

    专利信息


    专利号:US-2004053999-A1
    优先权日:1997-09-17
    标题 :Novel compounds and methods for synthesis and therapy
    发明人:BISCHOFBERGER NORBERT W; DAHL TERRENCE C; HITCHCOCK MICHAEL J M; KIM CHOUNG U; LEW WILLARD; LIU HONGTAO; MILLS ROGER G; WILLIAMS MATTHEW A
    摘要:Novel compounds are described. The compounds generally comprise an acidic group, a basic group, a substituted amino or N-acyl and a group having an optionally hydroxylated alkane moiety. Pharmaceutical compositions comprising the inhibitors of the invention are also described. Methods of inhibiting neuraminidase in samples suspected of containing neuraminidase are also described. Antigenic materials, polymers, antibodies, conjugates of the compounds of the invention with labels, and assay methods for detecting neuraminidase activity are also described.

    专利号:US-6225341-B1
    优先权日:1995-02-27
    标 题:Compounds and methods for synthesis and therapy
    发明人:BISCHOFBERGER NORBERT W; KIM CHOUNG U; LEW WILLARD; LIU HONGTAO; WILLIAMS MATTHEW A
    权利人:GILEAD SCIENCES INC
    摘要:Novel compounds are described. The compounds generally comprise an acidic group, a basic group, a substituted amino or N-acyl and a group having an optionally hydroxylated alkane moiety. Pharmaceutical compositions comprising the inhibitors of the invention are also described. Methods of inhibiting neuraminidase in samples suspected of containing neuraminidase are also described. Antigenic materials, polymers, antibodies, conjugates of the compounds of the invention with labels, and assay methods for detecting neuraminidase activity are also described.

    专利号:US-2003236435-A1
    优先权日:2002-05-15
    标题 :Synthesis of 2-alkylcysteine via substituted thiazoline ester

    专利号:EP-1529037-B1
    优先权日:2002-05-15
    标题 :Synthesis of 2-alkylcysteines, 2-(hydroxylated phenyl)-4-alkylthiazoline-4-carboxylic acids and derivatives thereof

    专利号:JP-2005538950-A
    优先权日:2002-05-15
    标题:Synthesis of 2-alkylcysteine, 2- (hydroxylated phenyl) -4-alkylthiazoline-4-carboxylic acids and their derivatives

    专利号:JP-2007001986-A
    优先权日:2002-05-15
    标 题 :Synthesis of 2-alkylcysteine, 2- (hydroxylated phenyl) -4-alkylthiazoline-4-carboxylic acids and their derivatives
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    主要参考文献

    参考标题:Oxidation Of Azides By The Hof.Ch3Cn: A Novel Synthesis Of Nitro Compounds
    作者:Mira Carmeli,Shlomo Rozen |发布日期:2006.6.1
    摘要:Aromatic Rings, Ketones, Nitriles, Halides, Alcohols, And Esters Are Tolerated. Sulfides React With Hof.Ch3Cn Usually At The Same Rate As Azides. Amines And Olefins, However, React Faster, So They Have To Be Protected First. Nitro Derivatives With Various Oxygen Isotopes Can Be Made Using The Labeled H18Of.Ch3Cn. In The Case Of Chiral Azides The Stereochemistry Around The Nitrogen-Bonded Carbons Is Retained

    合成参考文献


    摘要:Joosten, A.; Brioche, J., Science of Synthesis: Modern Strategies in Organofluorine Chemistry , (2024) 1, 24.
    参考文献:10.1186/1752-153x-5-26
    摘要:Esmaeili A, Hashemi E. Biotransformation of myrcene by Pseudomonas aeruginosa. Chemistry Central Journal. 2011 May 24;5(1). doi: 10.1186/1752-153x-5-26.
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