CAS: 1825-21-4; 1,2,3,4,5-Pentachloro-6-Methoxybenzene
该化合物是一种有机氯化合物,其特点是,含有五氯原子,附于一个活性结构,由甲基氧(-OCH3)组组成,与苯环捆绑在一起,该化合物一般是白色晶状固体,以其稳定性和耐降解性而闻名;五氯苯酚由于其抗微生物特性,主要用作杀真菌剂和木材防腐剂;该化合物还被公认为是五氯苯酚的一种降解产物,一种广泛使用的农药;该化合物具有疏水性,影响其在水中的溶解性,使其在有机溶剂中更易溶解;由于其氯含量,五氯苯酚可对环境和健康造成危害,从而引起对环境持久性和潜在生物蓄积性的关切;在处理该物质时,必须采取安全措施,因为它可能对水生生物产生毒性影响,而且如果摄入或吸入,则可能有害.
- 英文名称1,2,3,4,5-Pentachloro-6-Methoxybenzene
- 中文名称五氯苯甲醚
- IUPAC名称1,2,3,4,5-pentachloro-6-methoxybenzene
- 其它别名Anisole,2,3,4,5,6-pentachloro- (6CI,7CI,8CI); Benzene, pentachloromethoxy- (9CI); 2,3,4,5,6-Pentachloroanisole; Methyl pentachlorophenate; Methylpentachlorophenyl ether; PCP methyl ether; Pentachloroanisole; Pentachloromethoxybenzene; Pentachlorophenol methyl ether; Pentachlorophenylmethyl ether
- CAS编号1825-21-4
- MFCD编号:MFCD00129711
- EINECS号:625-770-0
- FDA UNII编号:14D125MH3W
- 分子式:C7H3Cl5O分子量:280.36
- 产品CID: 940632
- 产品分类分析化学 → 标准品 → 食品和饮料标准品
物理性质
- 熔点108-110°C
- 沸点309°C (760 Torr)
- 闪点127.1 °C
- 密度1.6178 (估算)
- PSA:9.23
- LogP:4.9622
- 蒸汽压0.000557 mmHg at 25 °C
- 溶解性Chloroform, Methanol (Slightly)
- 敏感性A halogenated ether derivative. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert. Simple aromatic halogenated organic compounds are very unreactive. Halogenated organics generally become less reactive as more of their hydrogen atoms are replaced with halogen atoms.
- 外观形态白色至类白色固体
- 储存条件0-6°C
MSDS等安全信息
欧盟法规
ECHA物质C&L通报上下游产品
diazomethane Pentachlorophenol tetrachloromethane para-iodoanisolehexachlorobenzene pentachlorophenyl-trichloromethyl ether chloromethyl-pentachlorophenyl ether 4-chloromethoxybenzene合成工艺路线路线简述
📜五氯酚置于n,N,N',N'-Tetrabutyl-N''-Methylguanidine Sodium Hydride体系中,化学反应 4.0H,反应生成五氯甲氧基苯
参考文献:五烷基胍作为醚化和酯化催化剂
标题:五烷基胍作为醚化和酯化催化剂
摘要:已经制备了几种五烷基胍,并且发现它们是用于由碳酸盐制备芳基和芳烷基醚以及用于苯酚与碳酸二甲酯甲基化的非常好催化剂.它们也可作为有效的催化剂,用于酸与烷基氯甲酸酯的酯化反应,而不是叔醇与乙酸酐的乙酰化反应.
Doi:10.1016/s0040-4020(01)89753-2
海关参考信息
- 2905110000-甲醇
2908110000-五氯苯酚
2908191000-对氯苯酚
2903911000-邻二氯苯 - 💡 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-2020047146-A1
优先权日:2017-03-17
标 题 :Hydroxyalkylated polyacrylamide surface coatings for in situ synthesis of dna arrays
发明人：MCGALL GLENN
权利人:CENTRILLON TECH HOLDINGS CORPORATION
摘要:The present disclosure relates to processes for derivatizing a surface of a substrate with a covalently bonded thin film of hydroxalkylated poly(acrylamide) as a platform for the synthesis of a biomolecule array. These processes can also be used to prepare a surface of a substrate for an in situ solid-phase synthesis of biomolecule array.
专利号:US-11149301-B2
优先权日:2017-03-17
标 题 :Preparation of universal spin-coatable amine-reactive surface coatings for biomolecule array fabrication
发明人：MCGALL GLENN
权利人:CENTRILLION TECH HOLDINGS CORP
摘要:The present disclosure relates to processes for derivatizing a surface of a substrate with a covalently bonded thin film of poly(methylsilsesquioxane)-bonded polymers as a platform for the synthesis of a biomolecule array. These processes can also be used to prepare a surface of a substrate for an in situ solid-phase synthesis of biomolecule array.
专利号:WO-2018169726-A1
优先权日:2017-03-17
标题 :Hydroxyalkylated polyacrylamide surface coatings for in situ synthesis of dna arrays
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
合成参考文献
摘要:Herve S et al; Chemosphere 17: 1945-61 (1988)
摘要:Meylan WM et al; Environ Sci Technol 28: 459-65 (1992)
摘要:Kuehl DW et al; Chemosphere 29: 523-5 (1994)
摘要:Franke C et al; Chemosphere 29: 1501-14 (1994)
摘要:
📝 需求与反馈
尽可能描述清楚需求与问题信息
