CAS: 59293-67-3; (2,4-Dichlorophenyl)Methanethiol

该化合物是一种有机硫化合物,其特征是,苯环上有一个硫醇(-SH)组,该组附属于苯环,在2和4个位置上又用两个氯原子替换.该化合物一般是无色的,可粉黄,有明显的气味;有机溶剂中可溶解,但因其缺水芳香结构,水溶解性有限;氯原子的存在可增强它的再活动性,使其在各种化学合成和应用中有用,包括作为生产农用化学品和药品的中间体;此外,硫醇组有助于其作为消毒剂的潜力和形成脱硫联结的能力.在处理该化合物时,有必要采取安全防范措施,因为吸入或皮肤接触可能会对健康造成危险,因此,氯原子应储存在冷却,通风不相容的物质之外的地区.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

dimethyl-dithi°Carbamic acid-(2,4-dichloro-benzyl ester) 2,4-dichloro-1-{[(2,4-dichlorobenzyl)disulfanyl]methyl}benzene 2,4-Dichlorobenzyl chloride thiourea ethyl 2-(2, 4-dichlorophenyl)acetate 5'-O-Dimethoxytritylthymidine-3'-O-[β-cyanoethyl-(S-2,4-dichlorobenzyl)]-phosphorodithioate 5'-O-tritylthymidine-3'-O(S-2,4 dichlorobenzylmethyl)methylphosphonothioate

合成工艺路线路线简述

    📜Rrd-251盐酸盐置于sodium Hydroxide体系中,化学反应生成 2,4-二氯苄硫醇
    参考文献:Tait; Di Bella; Bondi,Il Farmaco,1990,Vol. 45,# 6,P. 617-630
    标题:Tait; Di Bella; Bondi,Il Farmaco,1990,Vol. 45,# 6,P. 617-630

    海关参考信息

    专利信息


    专利号:US-7273933-B1
    优先权日:1998-02-26
    标 题 :Methods for synthesis of oligonucleotides
    发明人:KROTZ ACHIM H; RAVIKUMAR VASULINGA T
    权利人:ISIS PHARMACEUTICALS INC
    摘要:Improved methods for synthesis of oligonucleotides and other phosphorus-linked oligomers are disclosed. The methods include the use of aromatic solvents, alkyl aromatic solvents, halogenated aromatic solvents, halogenated alkyl aromatic solvents, or aromatic ether solvents to achieve deprotection of protected hydroxyl groups.

    专利号:US-5714597-A
    优先权日:1994-07-07
    标题:Use of carbocation scavenger during oligonucleotide synthesis
    发明人:RAVIKUMAR VASULINGA; ANDRADE MARK; MULVEY DENNIS; COLE DOUGLAS L
    权利人:ISIS PHARMACEUTICALS INC
    摘要:During the synthesis of oligonucleotides and phosphate linked oligomers, a carbocation scavenging agent is employed to increase the overall yield. The carbocation scavenging agent is used in conjunction with an acidic solution employed during the deprotection step.

    专利号:US-5331096-A
    优先权日:1992-04-01
    标题 :2- and 3-sulfur derivatives of 1,5-iminosugars
    发明人:KOSZYK FRANCIS J; MUELLER RICHARD A
    权利人:SEARLE & CO
    摘要:Novel derivatives of 1-deoxynojirimycin are disclosed which have thio or sulfinyl substituents at C-2 or C-3. These compounds are useful inhibitors of lentiviruses such as visna virus and human immunodeficiency virus. Methods of chemical synthesis of these derivatives and intermediates therefor are also disclosed.

    专利号:US-5342951-A
    优先权日:1992-04-01
    标题:2- and 3-sulfur derivatives of 1,5-iminosugars
    发明人:KOSZYK FRANCIS J; MUELLER RICHARD A
    权利人:SEARLE & CO
    摘要:Novel derivatives of 1-deoxynojirimycin are disclosed which have thio or sulfinyl substituents at C-2 or C-3. These compounds are useful inhibitors of lentiviruses such as visna virus and human immunodeficiency virus. Methods of chemical synthesis of these derivatives and intermediates therefor are also disclosed.

    专利号:US-5268482-A
    优先权日:1992-04-01
    标 题:2- and 3-sulfur derivatives of 1,5-iminosugars
    发明人:KOSZYK FRANCIS J; MUELLER RICHARD A
    权利人:SEARLE & CO
    摘要:Novel derivatives of 1-deoxynojirimycin are disclosed which have thio or sulfinyl substituents at C-2 or C-3. These compounds are useful inhibitors of lentiviruses such as visna virus and human immunodeficiency virus. Methods of chemical synthesis of these derivatives and intermediates therefor are also disclosed.

    专利号:US-5210264-A
    优先权日:1992-01-10
    标 题 :S-(2,4-dichlorobenzyl)-β-cyanoethyl phosphorothioate diester
    发明人:YAU ERIC K
    权利人:ISIS PHARMACEUTICALS INC
    摘要:The compound S-(2,4-dichlorobenzyl)-β-cyanoethyl phosphorothioate diester is disclosed as useful in the synthesis of phosphorothioate oligonucleotides. In certain embodiments of the invention, this reagent is used to prepare 3'-S-(alkaryl) phosphorothioates. The β-cyanoethyl blocking group can be removed and the resulting diester reacted with a nucleotide having a free 5'-hydroxyl group to yield compounds of the structure: ##STR1## where X is H, a first blocking group, a nucleoside, a nucleotide or an oligonucleotide; Y is H, a second blocking group, a nucleotide or an oligonucleotide; R is an alkaryl or aryl group; n is an integer greater than 0; and Bx is a heterocyclic base. Deblocking of the S-alkaryl or S-aryl moiety yields a phosphorothioate oligonucleotide.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:An Improved Method For The Synthesis Of Disulfides By Periodic Acid And Sodium Hydrogen Sulfite In Water
    作者:Khalid M. Khan,Muhammad Taha,Fazal Rahim,Muhammad Ali,Waqas Jamil,Shahnaz Perveen,M. Iqbal Choudhary |发布日期:2010.7.1
    摘要:An Improved Method For The Synthesis Of Disulfide In Water By Using Periodic Acid And Sodium Hydrogen Sulfite Was Developed.

    合成参考文献


    摘要:Kashemirov, B. A.; Błażewska, K.; Justyna, K.; Lyu, J.; McKenna, C. E., Science of Synthesis Knowledge Updates, (2021) 1, 483.
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