CAS: 1073-29-6; 2-(Methylthio)Phenol

相似化合物

1073-72-9 29549-60-8 2388-73-0

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CAS号2388-73-0 2-甲氧基茴香硫醚 | CAS号99346-84-6 magnesium,methy... | CAS号108-95-2 苯酚 | CAS号624-92-0 二甲基二硫醚 | CAS号7429-90-5 铝片 | CAS号10026-11-6 四氯化锆 | CAS号1121-24-0 2-羟基苯硫酚 | CAS号74-88-4 碘甲烷 | CAS号1073-72-9 4-(甲硫基)苯酚 | CAS号74-83-9 溴甲烷 | CAS号27489-33-4 2-(甲基磺酰)苯酚 | CAS号72955-86-3 2-[2-(甲硫基)苯氧基]乙胺 | CAS号1074-02-8 2-(甲基亚磺酰)苯酚 | CAS号2388-73-0 2-甲氧基茴香硫醚 | CAS号66264-56-0 1-[4-hydroxy-3-... | CAS号67127-64-4 2-羟基-3-(甲基)苯甲酸 | CAS号57728-82-2 (2-methylsulfan... | CAS号38452-13-0 1-methoxy-2-met...

Magnesium,Methylsulfanylbenzene,Bromide置于air体系中,用 四氢呋喃 用作溶剂,-25.0 °C,1.72 Mpa 条件下,反应 0.06H,以75%的收率获得2-羟基茴香硫醚
参考文献:格氏试剂的需氧氧化连续流式合成功能化苯酚
标题:格氏试剂的需氧氧化连续流式合成功能化苯酚
摘要:苯酚是化学工业中的重要化合物.描述了在连续的气液分段流系统中使用压缩空气通过直接氧化芳基格氏试剂来制备苯酚的一种经济,绿色的方法.该工艺可耐受各种官能团,包括对氧化敏感的官能团,例如烯烃,胺和硫醚.通过将苯并炔介导的芳基镁中间体的在线生成与好氧氧化相集成,建立了一种能够以模块化方式制备2-官能化苯酚的简便的三步单流方法.
Doi:10.1002/anie.201310572

专利信息

专利号:US-12421534-B2
优先权日:2021-11-10
标 题 :Engineered enzymes and method for the synthesis of diverse tyrosine analogs
发明人：ALMHJELL PATRICK J; ARNOLD FRANCES H
权利人:CALIFORNIA INST OF TECHN
摘要:Provided herein is an engineered tryptophan synthase β-subunit (TrpB) that catalyzes the synthesis of tyrosine, tyrosine analogs, or salts thereof. Also provided herein are methods for preparing tyrosine, tyrosine analogs, or a salt thereof using the engineered TrpB described herein.

专利号:US-2012226018-A1
优先权日:2009-11-16
标 题:Process for the Synthesis of Ac-Arg-Cyclo(Cys-D-Ala-His-D-Phe-Arg-Trp-Cys)-NH2
发明人：DONG ZHENG XIN
权利人:DONG ZHENG XIN; IPSEN PHARMA SAS
摘要:The present invention relates to a novel process for the synthesis of the melanocortin analog, Ac-Arg-cyclo(Cys-D-Ala-His-D-Phe-Arg-Trp-Cys)-NH 2 , using solution-phase peptide chemistry.

专利号:US-9115179-B2
优先权日:2012-06-22
标题 :Synthesis of beta-turn peptidomimetic cyclic compounds
发明人：LAMA TERESA; PASCAL JEANICK
权利人:MIMETOGEN PHARMACEUTICALS INC
摘要:The present invention relates to methods of preparing β-turn cyclic peptidomimetic compounds and intermediates thereof. Particularly, the present invention relates to a process for the synthesis of β-turn cyclic peptidomimetic compounds of formula I: n nwhere R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , L 2 , X, Y and n are as defined in the specification.n n The present invention provides a more efficient route for preparing β-turn cyclic peptidomimetic compounds and intermediates thereof.

专利号:US-8202985-B2
优先权日:2005-10-31
标 题:Monomer compositions for the synthesis of polynucleotides, methods of synthesis, and methods of deprotection
发明人：DELLINGER DOUGLAS J; TIMAR ZOLTAN; SIERZCHALA AGNIESZKA; DELLINGER GERALDINO; CARUTHERS MARVIN H
权利人:DELLINGER DOUGLAS J; TIMAR ZOLTAN; SIERZCHALA AGNIESZKA; DELLINGER GERALDINO; CARUTHERS MARVIN H; AGILENT TECHNOLOGIES INC; UNIV COLORADO
摘要:Nucleotide monomers, polynucleotides, methods of making each, and methods of deprotecting each, are disclosed. An embodiment of the nucleotide monomer, among others, includes a nucleotide monomer having a heterobase protecting group selected from structures I through III as described herein. An embodiment of the polynucleotide, among others, includes a plurality of nucleotide moieties having a heterobase protecting group selected from one of structures I through III as described herein.

专利号:US-7759471-B2
优先权日:2005-10-31
标题 :Monomer compositions for the synthesis of RNA, methods of synthesis, and methods of deprotection
发明人：DELLINGER DOUGLAS J; TIMAR ZOLTAN; SIERZCHALA AGNIESZKA; DELLINGER GERALDINE; CARUTHERS MARVIN H
权利人:AGILENT TECHNOLOGIES INC; UNIV COLORADO
摘要:Nucleotide monomers, polynucleotides, methods of making each, methods of deprotecting each, and the like are disclosed herein.

专利号:EP-0264802-B1
优先权日:1986-10-21
标 题:Synthesis of peptide-aminoalkyl amides and peptide hydrazides by the solid phase method
摘要:Compounds of the formula I in which A is hydrogen or an amino protective group, B is an amino acid residue, X is alkylene or aralkylene, Y<1>, Y<2>, Y<3> and Y<4> are identical or different and are hydrogen, methyl, methoxy or nitro, V is hydrogen or a carboxyl protective group, W is -[CH2]n- or -O-[CH2]n-, m is 0 or 1, n is 0 to 6 and p is 0 to 5, are prepared as described and used in the solid-phase synthesis.