- 相似结构搜索
- InChIKey: LYXCVHLXCNLHFW-UOUKXZINSA-L
- 1S/C16H12N2O7S2.2Na/c19-15-8-1-10-9-13(27(23,24)25)6-7-14(10)16(15)18-17-11-2-4-12(5-3-11)26(20,21)22;;/h1-9,19H,(H,20,21,22)(H,23,24,25);;/…
- 计算化学: 氢键受体数9.0氢键供体数1.0可旋转键数2.0
物理性质
- 熔点Decomposes without melting when heated to 390 deg C
- PSA:172.62
- LogP:3.1415
- 外观形态微红色-棕色粉末
- 产品应用直接黄R(cas:1325-37-7)的用途:直接黄R可用于棉,黏胶纤维及其针织品染色,得鲜艳红光黄色.也可用于蚕丝,羊毛的染色.较多用于黏胶纤维与蚕丝交织物染色.也可用于纸张及棉丝织物的染色匀染性和移染性均较差.染色后需经固色剂处理,以提高湿牢度.本品具有较强的光脆损作用.
- 性质描述直接黄R(cas:1325-37-7)的化学性质:棕色粉末.溶于水呈红光黄色,微溶于乙二醇乙醚,不溶于其他有机溶剂.其水溶液加浓盐酸呈橄榄黄色,加浓氢氧化钠产生金橙色沉淀.于浓硫酸中呈暗红色,稀释后呈暗黄色,并伴有棕色沉淀.于浓硝酸中部分溶解,呈黄光棕色转橄榄色.于浓盐酸中部分溶解呈黑色.染色时遇铜离子色光偏绿,遇铁离子色光稍暗红,遇锌离子和氨变成浅黄光橙色.
欧盟法规
ECHA物质C&L通报REACH预注册海关参考信息
- 2902902000-精萘
2908199090-其他酚的卤化衍生物
2908999090-其他酚的硝化衍生物
2918290000-其他含酚基羧酸 - 💡 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-2023313255-A1
优先权日:2020-07-15
标题:Massively Parallel Enzymatic Synthesis of Polynucleotides
发明人:HORGAN ADRIAN; LACHAIZE HENRI; VERARDO DOMIANO; GODRON XAVIER
权利人:DNA SCRIPT
摘要:The invention is directed to methods and compositions for inkjet assisted synthesis of a plurality of polynucleotides at reaction sites on a substrate using template-free polymerases, such as, terminal deoxynucleotidyl transferases (TdTs). Compositions of the invention include formulations of synthesis reagents for inkjet delivery including, but not limited to, TdT coupling reaction buffers and 3′-O-protected dNTP monomers.
专利号:US-10040752-B2
优先权日:2015-08-24
标 题 :Synthesis of levomethadone hydrochloride or dextromethadone hydrochloride and methods for use thereof
发明人:MKRTCHYAN GNEL; YAO QINGWEI
权利人:CODY LABORATORIES INC
摘要:Highly efficient methods for synthesis of levomethadone hydrochloride or dextromethadone hydrochloride are provided starting from D-alanine, or L-alanine, respectively, with retention of configuration. Methods for treating a subject are provided comprising administering a composition comprising an effective amount of levomethadone hydrochloride having not more than 10 ppm dextromethadone.
专利号:WO-2012120543-A1
优先权日:2011-03-09
标 题 :A single step process for synthesis of yellow dye -11 of consistent colour tone
发明人:KULKARNI AMOL ARVIND; JOSHI RAMESH ANNA; JOSHI ROHINI RAMESH
权利人:COUNCIL SCIENT IND RES; KULKARNI AMOL ARVIND; JOSHI RAMESH ANNA; JOSHI ROHINI RAMESH
摘要:Yellow due 11 is a useful dye with several application in the industry. The available literature in the synthesis of this dye results in non uniform colour tone. This issue in prior art is addressed by disclosing a batch as well continuous single condensation step process for synthesizing the yellow dye 11 with on-line uv monitoring system to ensure colour tone uniformity.
专利号:US-10882884-B2
优先权日:2016-05-18
标题:Stereoselective synthesis of phosphorothioate oligoribonucleotides
发明人:HALL JONATHAN; LI MEILING
权利人:ETH ZUERICH
摘要:The present invention relates to chiral phosphoramidites represented by formula (Ia) or formula (Ib) n n n n n n n n n n n n as novel monomers for the synthesis of stereodefined phosphorothioate MOE oligonucleotides. Furthermore, the present invention relates to a method for synthesizing stereodefined phosphorothioate MOE oligonucleotides using said novel chiral phosphoramidites.
专利号:WO-2024153643-A1
优先权日:2023-01-16
标 题 :Inkjet-assisted enzymatic nucleic acid synthesis
发明人:MOGHADDAM NICOLAS; ADELIZZI BEATRICE; LOMAN TESSA; VERARDO DAMIANO; RODRIGUEZ-PINZON DANIEL; HORGAN ADRIAN
权利人:DNA SCRIPT
摘要:Methods, devices, and compositions are provided for inkjet-assisted synthesis of a plurality of polynucleotides at reaction sites on a substrate using template-free polymerases, such as, terminal deoxynucleotidyl transferases (TdTs). Compositions include printable stabile formulations of synthesis reagents for inkjet delivery including, but not limited to, template-free polymerases, divalent cations, and nucleotides.
专利号:US-6777554-B2
优先权日:2001-02-05
标题 :Preparation of N-methylparoxetine and related intermediate compounds
发明人:FINKELSTEIN NINA
权利人:TEVA PHARMA
摘要:The present invention provides a process for preparing N-methylparoxetine, an intermediate in the synthesis of paroxetine, by reacting sesamol-tetrabutylammonium salt with CIPMA. The present invention is not limited to the synthesis of N-methylparoxetine, but also includes other similar compounds.