CAS: 556-61-6; Methyl Isothiocyanate

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统一分类与标签压力设备指令-第1组危险流体REACH注册ECHA物质工作场所安全标识要求ECHA物质C&L通报REACH预注册废弃物危险特性清单

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CAS号75-15-0 二硫化碳 | CAS号593-51-1 一甲胺盐酸盐 | CAS号463-71-8 硫光气 | CAS号74-89-5 氨基甲烷 | CAS号137-41-7 N-甲基二硫代氨基甲酸钾 | CAS号815-06-5 N-甲基三氟乙酰胺 | CAS号593-75-9 甲胩 | CAS号17986-01-5 methylimino(tri... | CAS号52664-26-3 ethyl N-methylc... | CAS号79645-01-5 1,3-dimethyl-1-... | CAS号107366-68-7 N-methylthiophe... | CAS号1076-72-8 Mth-dl-亮氨酸 | CAS号107401-74-1 akos ussh-4110200 | CAS号5422-44-6 1-甲基-5-氨基四氮唑 | CAS号38942-51-7 5-苯基-4-甲基-4氢-3-... | CAS号34839-70-8 甲硫米特 | CAS号4311-88-0 Necrostatin-1 | CAS号38942-50-6 3,4-二甲基-1H-1,2,... | CAS号4807-55-0 3-甲基罗丹宁 | CAS号534-13-4 N,N′-二甲基硫脲

合成工艺路线路线简述

    N1,N3-Dimethyl-N1-Nitrosothiourea置于potassium Phosphate Buffer体系中,化学反应 12.0H,以50%的收率获得产物异硫氰酸甲酯
    参考文献:Stereoelectronic Control In The Aqueous Decomposition Of Novel Nitrosothioureas
    标题:Stereoelectronic Control In The Aqueous Decomposition Of Novel Nitrosothioureas
    摘要:
    DOI:10.1021/jo00170A006

    专利信息


    专利号:US-4049710-A
    优先权日:1976-02-24
    标题:Novel carbamimidoyl chlorides and their use in the synthesis of herbicidal triazinediones
    发明人:TOCKER STANLEY
    权利人:DU PONT
    摘要:Carbamimidoyl chlorides of the formula: WHERE R2 is alkyl of 1-4 carbon atoms are useful as intermediates in the synthesis of herbicidal triazinediones of the formula: where R1 is certain organic radicals.

    专利号:US-10858414-B2
    优先权日:2018-03-09
    标 题:Chemo-enzymatic synthesis of semaglutide, liraglutide and GLP-1
    发明人:NUIJENS TIMO; TOPLAK ANA; QUAEDFLIEG PETER JAN LEONARD MARIO
    权利人:ENZYPEP B V
    摘要:The invention relates to a method for preparing a coupling product having the sequence P q -W v -His-X-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Y-Glu-Phe-Ile-Ala-Trp-Leu-Val-Z-Gly-Arg-Gly. The method includes enzymatically couplingn (a) a peptide C-terminal ester or thioester having a first peptide fragment represented by the formula P q -W v -His-X-Glu-(thio)ester; and (b) a peptide nucleophile having an N-terminally unprotected amine having a second peptide fragment with the sequence H-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Y-Glu-Phe-Ile-Ala-Trp-Leu-Val-Z-Gly-Arg-Glyn whereinn P represents a protective group at the N-terminal α-amino function of the peptide C-terminal ester or thioester and q is an integer having a value of 1 or 0; W represents one or more amino acid residues, which may be the same or different and v is an integer having a value of 1 or more representing the number of amino acid residues W; X is Ala or an α-amino-isobutyric acid unit (Aib); Y is Lys, which Lys has a free side-chain ε-amino group or a side-chain ε-amino group that is protected with a protective group or a side-chain ε-amino group that is functionalized with an amino acid or another functional group; and n Z is Arg or Lys.

    专利号:US-10920258-B2
    优先权日:2018-03-09
    标题 :Chemo-enzymatic synthesis of semaglutide, liraglutide and GLP-1
    发明人:NUIJENS TIMO; TOPLAK ANA; QUAEDFLIEG PETER JAN LEONARD MARIO
    权利人:ENZYPEP B V
    摘要:A method for synthesizing a peptide having the sequence His-X-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Y-Glu-Phe-Ile-Ala-Trp-Leu-Val-Z-Gly-Arg-Gly is disclosed. The method includes enzymatically coupling:n (a) a peptide C-terminal ester or thioester having a first peptide fragment with the sequence His-X-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-(thio)ester; and (b) a peptide nucleophile having an N-terminally unprotected amine having a second peptide fragment with the sequence H-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Y-Glu-Phe-Ile-Ala-Trp-Leu-Val-Z-Gly-Arg-Gly; wherein:n X is Ala or an α-amino-isobutyric acid (Aib) residue; Y is Lys, which Lys has a free side-chain ε-amino group or of which Lys the side-chain ε-amino group is protected with a protective group or of which Lys the side-chain ε-amino group is functionalized with an amino acid or another functional group; and Z is Arg or Lys.

    专利号:EP-1892237-A1
    优先权日:2004-01-28
    标 题 :Vinylchloroformate-free synthesis of vinyl and allyl(thio)carbamates
    发明人:SEELYE DAVID E; KUNZLER JAY F; SALAMONE JOSEPH C
    权利人:BAUSCH & LOMB
    摘要:The invention generally relates to methods of forming allyl(thio)carbamates and more particularly to a method of synthesizing allyl(thio)carbamates that does not necessitate the use of phosgene and organomercury intermediates.

    专利号:US-7402689-B2
    优先权日:2004-01-28
    标 题 :Vinylchloroformate-free synthesis of vinyl and allyl(thio) carbamates
    发明人:SEELYE DAVID E; KUNZLER JAY F; SALAMONE JOSEPH C
    权利人:BAUSCH & LOMB
    摘要:The invention generally relates to methods of forming vinyl(thio)carbamates and more particularly to a vinylchloroformate-free method of synthesizing (N-vinyloxycarbonyl)-3-aminopropyltris(trimethylsiloxysilane).

    专利号:WO-2024256370-A1
    优先权日:2023-06-13
    标 题 :Synthesis of glufosinate using an amidase-based process
    发明人:ZIMMERMANN GUNTHER; POTT MORITZ STEFAN
    权利人:BASF SE
    摘要:The present invention relates to a method of preparing glufosinate, comprising the steps of hydrolysing an N-carbamoyl glufosinate amide with an Amidase enzyme to form an N- carbamoyl amino acid compound followed by cleaving off the carbamoyl moiety of said N- carbamoyl amino acid compound.
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    合成参考文献


    参考文献:10.1016/j.taap.2005.10.004
    摘要:Pruett SB, Fan R, Zheng Q. Involvement of three mechanisms in the alteration of cytokine responses by sodium methyldithiocarbamate. Toxicol Appl Pharmacol. 2006 Jun 01;213(2):172–8. doi: 10.1016/j.taap.2005.10.004.
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