CAS: 5490-92-6; (9H-Xanthen-9-yl)Methanol

该化合物是有机化合物,其特点是其Xanthene结构,由包括苯环和中央氧原子的引信环系统组成;该化合物是附于Xanthene核心的氢甲基组(-CH2OH),有助于其反应和潜在应用;它一般是无色的,可粉黄的固体或液体,视其纯度和形态而定;氢-甲基组的存在允许氢结合,影响其在水和酒精等极溶剂中的溶性. 9H-Xanthen-9-ylm乙醇因其荧光特性和在染料应用中的潜在用途,对各个领域,包括有机合成和材料科学,都感兴趣.此外,它可作为合成其他Xanne衍生物的前体,这些衍生物对于发展荧光探测器和感应具有价值.应参考安全数据,以便处理和储存所有化学物质.

结构式图片

上下游产品

xanthene-9-carboxylic acid 9H-xanthene-9-carboxylic acid methyl ester benzoic acid xanthen-9-ylmethyl ester xanthene 9-iodomethyl-9H-xanthene 9-xanthylmethyl p-nitrophenylcarbonate

合成工艺路线路线简述

  • 合成目标产物 9H-Xanthene-9-Methanol 主要起始原料 Xanthene-9-Carboxylic Acid
  • (文献来源)合成步骤主要原料 Xanthene-9-Carboxylic Acid
📜占吨-9-甲酸甲酯置于lithium Aluminium Tetrahydride,乙醚体系中,化学反应生成 9H-氧杂蒽-9-甲醇
参考文献:Studies In The Wagner-meerwein Rearrangement. Part Ii
标题:Studies In The Wagner-meerwein Rearrangement. Part Ii
摘要:Dibenz[b,F]Oxepin及其10-甲基衍生物已通过合适的苯并二氧杂环衍生物的环扩张制备.2-氟菲是由2-氟芴合成的.
DOI:10.1139/v57-147

海关参考信息

专利信息


专利号:US-5101059-A
优先权日:1989-12-05
标 题 :Amino acid protecting groups
发明人:CARPINO LOUIS A; WU AN-CHUU
权利人:RES CORP TECHNOLOGIES INC
摘要:This invention relates to compounds of the formula a compound of the formula ##STR1## wherein X is O, CR 7 R 8 , S or NR 9 wherein R 7 and R 8 are independently hydrogen, or lower alkyl, and R 9 is lower alkyl; n n is 0 or 1; n R 1 and R 2 are independently hydrogen, lower alkyl, monoorganosilyl, diorganosilyl, triorganosilyl, halogen, aryl, or nitro; n R 3 is hydrogen, lower alkyl, monoorganosilyl, diorganosilyl, triorganosilyl, halogen, 9-fluorenylalkyl, cycloalkyl, aryl or aralkyl; n R 4 and R 5 are independently hydrogen, lower alkyl, or aryl or one of R 4 and R 5 is 9-fluorenyl; n R 6 is H or COZ wherein Z is an amino acid, a peptide residue or a leaving group; and n with the provisos that when n is 0 and R 3 is hydrogen, R 1 and R 2 are not hydrogen, halogen or nitro; that when n is 0 and R 3 is lower alkyl, R 1 and R 2 are not hydrogen; and that when X is O or CR 7 R 8 wherein R 7 and R 8 are H, that R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 are not all simultaneously H. The compounds of the present invention are useful in peptide synthesis as blocking or protecting groups for reactive groups. The present invention is also directed to a method of protecting a reactive group of an organic molecule during a reaction which modifies a portion of the molecule other than the protected group.

专利号:CN-119390724-A
优先权日:2024-09-19
标 题 :Synthesis method of phosphorous acid diester compound

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品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

合成参考文献


摘要:von Angerer, S., Science of Synthesis, (2004) 17, 680.
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