- 英文名称4,4-Isopropylidenebis[2-(2,6-Dibromophenoxy)Ethanol](Flakes Or Chunks)
- 中文名称2,2-双[4-(2-羟基乙氧基)-3,5-二溴苯基]丙烷
- IUPAC名称2,2'-((propane-2,2-diylbis(2,6-dibromo-4,1-phenylene))bis(oxy))bis(ethan-1-ol)
- 其它别名2,2-Bis{3,5-dibromo-4-(2-hydroxyethoxy)phenyl}propane
- CAS编号4162-45-2
- MFCD编号:MFCD00059603
- EINECS号:224-005-4
- FDA UNII编号:Y6AMX5NV4O
- 分子式:C19H20Br4O4分子量:631.98
- 产品CID: 1430322
- 产品分类化学试剂 → 有机试剂 → 芳香醇
物理性质
- 熔点107 °C(文献)
- 沸点582.1±50.0 °C at 760 mmHg
- 闪点305.8±30.1 °C
- 密度1.8±0.1 g/cm3
- pKa:13.76±0.10(预测)
- PSA:58.92
- LogP:4.98
- 折射率1.621
- 蒸汽压0.0±1.7 mmHg at 25°C
- 溶解性DMSO (Slightly), Methanol (Slightly)
- 敏感性常温常压下稳定, 热稳定性很好。
- 外观形态白色至类白色固体
- 储存条件防潮, 冰箱, 置于惰性气氛下
- 产品应用2,2-双[4-(2,3-二溴丙氧基)-3,5-二溴苯基]丙烷 (4162-45-2)本品为反应型阻燃剂,可用于聚酯,环氧树脂,聚氨酯,也可用于ABS树脂,本品还可作为反应型阻燃剂用于聚酯纤维.
- 性质描述2,2-双[4-(2,3-二溴丙氧基)-3,5-二溴苯基]丙烷 (4162-45-2)的性质如下:1,熔点113~119°C.分解温度:质量减少5%开始温度不低于300°C2,白色粉末.3,可溶于甲乙酮,甲醇,二氯甲烷,苯及丙酮,微溶于水.4,质量损失5%的温度322°C,热稳定性很好.
欧盟法规
ECHA物质ECHA物质C&L通报REACH预注册海关参考信息
- 2902600000-乙苯
2902700000-异丙基苯
2905310000-1,2-乙二醇
2908199090-其他酚的卤化衍生物 - 💡 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-2009111737-A1
优先权日:1999-05-24
标题:Novel antibacterial agents
发明人:CHRISTENSEN BURTON G; MORAN EDMUND J; GRIFFIN JOHN H; JUDICE J KEVIN; MU YONGQI; PACE JOHN L; MAMMEN MATHAI; AGGEN JAMES
权利人:CHRISTENSEN BURTON G; MORAN EDMUND J; GRIFFIN JOHN H; JUDICE J KEVIN; MU YONGQI; PACE JOHN L; MAMMEN MATHAI; AGGEN JAMES
摘要:This invention relates to novel multibinding compounds (agents) that are antibacterial agents. The multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands in their monovalent (i.e., unlinked) state have the ability to bind to a an enzyme involved in cell wall biosynthesis and metabolism, a precursor used in the synthesis of the bacterial cell wall and/or the bacterial cell surface thereby interfere with the synthesis and/or metabolism of the cell wall. In particular the multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands hasn a ligand domain capable of binding to penicillin binding proteins, a transpeptidase enzyme, a substrate of a transpeptidase enzyme, a beta-lactamase enzyme, pencillinase enzyme, cephalosporinase enzyme, a transglycoslase enzyme, or a transglycosylase enzyme substrate; Preferably, the ligands are selected from the beta lactam or glycopeptide class of antibacterial agents.
专利号:US-7179794-B2
优先权日:1998-06-08
标题 :Multivalent macrolide antibiotics
发明人:GRIFFIN JOHN H; PACE JOHN L
权利人:THERAVANCE INC
摘要:Disclosed are multibinding compounds which include macrolide antibiotics, aminoglycosides, lincosamides, oxazolidinones, streptoramins, tetracycline and/or other compounds which bind to bacterial ribosomal RNA and/or to one or more proteins involved in ribosomal protein synthesis in the bacterium, which are useful in treating bacterial infections. The compounds adversely affect protein expression and have an antibacterial effect. The multibinding compounds of this invention containing from 2 to 10 ligands covalently attached to one or more linkers. Each ligand is macrolide antibiotic, aminoglycoside, lincosamide, oxazolidinone, streptogramin, tetracycline or other compound which binds to bacterial ribosomal RNA and/or one or more proteins involved in ribosomal protein synthesis in the bacterium.