CAS: 15015-57-3; Bis(4-Hydroxyphenyl) Disulfide

该化合物是有机化合物,其特点是存在两个氢氧化物组和一个分硫化物链接,该化合物的特点是双苯结构,其中每个苯环在副位置被一个氢氧化物组所取代,有助于其作为抗氧化剂和各种应用中稳定剂的潜力;脱硫物联结具有独特的化学特性,使其与聚合物化学和材料科学有关,特别是在橡胶和塑料的开发方面;通常在室温下具有固态,并可能表现出有机溶剂中的中溶性;该化合物的再活动可能受到氢氧基组的影响,这些组可参与氢的联结和其他相互作用;由于其结构特性,BIS(4-HYDROXYPHEL) DISUFULIDE还可能对药化学产生影响,特别是在研究具有潜在治疗作用的化合物方面.应当参考安全数据,以便处理和使用,因为与所有化学物质有关.

英文名称Bis(4-Hydroxyphenyl) Disulfide
中文名称双(4-羟苯基)二硫醚
IUPAC名称4,4'-disulfanediyldiphenol
其它别名Di(4-Hydroxyphenyl)-Disulfide; L-Glutamic Acid, N-(N-Acetyl-L-Beta-Aspartyl)-; 4,4'-Dithiodiphenol; 4-Hydroxyphenyldisulfide; Bis(4-Hydroxyphenyl)Disulfid
CAS编号15015-57-3
MFCD编号:MFCD00020164
EINECS号:805-758-3
分子式:C12H10O2S2
分子量:250.34
产品CID: 726954
产品分类有机原料→分子砌块→芳环类化合物→苯类化合物

相似结构搜索
产品信息参考;;
InChIKey: XGKGITBBMXTKTE-UHFFFAOYSA-N
InChI=1S/C12H10O2S2/c13-9-1-5-11(6-2-9)15-16-12-7-3-10(14)4-8-12/h1-8,13-14H…
计算化学: 氢键受体数4.0氢键供体数2.0可旋转键数3.0

相似化合物

21101-56-4 5335-87-5 882-33-7

物理性质

熔点150.0-154.0 °C
沸点437.9°C at 760 mmHg
闪点212.5±23.3 °C
密度1.4±0.1 g/cm3
PSA:40.46
LogP:3.8972
折射率1.752
蒸汽压0.0±1.1 mmHg at 25°C
溶解性溶于甲醇
外观形态固体;White to Light yellow powder to crystal
储存条件2-8°C, stored under nitrogen
产品应用该化合物是* 甲状腺素* 的抗体抑制剂;它以激光蛋白(KD=7.04 ΜM)为对象,抑制了* PSEUDOMONAS AERUGINOSA* 法定人数感测系统,从而防止* PSODOMONAS AREUGINOSO* 引起食物破坏.

MSDS等安全信息

GHS象形图
GHS符号GHS07 & GHS09;
注释: Exclamation mark & Environment
危险类别皮肤腐蚀/刺激类别2
严重眼刺激类别2
特定目标器官毒性 - 单次接触类别3
严重眼刺激类别2A
急性毒性类别4(经口)
水生急性毒性类别1
水生慢性毒性类别1
警示词Warning(警告)
危险描述H315 |造成皮肤刺激.
H319 |造成严重眼刺激.
H335 |可能引起呼吸道刺激.
H302 |吞咽有害.
H400 |对水生生物毒性极大.
H410 |对水生生物毒性极大并具有长期持续影响.
防范说明P264-P280-P302+P352-P362+P364
危险品标志Xi

欧盟法规

ECHA物质C&L通报

上下游产品

合成工艺路线路线简述

4,4'-二甲氧基二苯二硫置于盐酸体系中,用吡啶用作溶剂,化学反应 0.17H,以28%的收率获得4,4'-二羟基二苯二硫醚
参考文献:Lalonde,Robert T.; Eckert,Timothy S.,Canadian Journal Of Chemistry,1981,Vol. 59,P. 2298-2302
标题:Lalonde,Robert T.; Eckert,Timothy S.,Canadian Journal Of Chemistry,1981,Vol. 59,P. 2298-2302

海关参考信息

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
2905199090-其他饱和一元醇
💡 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-5629394-A
优先权日:1992-12-17
标题 :Direct synthesis by living cationic polymerization of nitrogen-containing polymers
发明人：CHERADAME HERVE M; CHEN FRANK J; STANAT JON E R; NGUYEN HUNG A; TABAR BEHROOZ R
权利人:EXXON CHEMICAL PATENTS INC
摘要:A method is provided for the direct synthesis by living cationic polymerization of novel polymeric materials functionalized with desirable nitrogen-containing functional groups such as terminal azido, cyano, carbonylamino, cyanato, thiocyanato or thiocarbonylamino groups. Polymerization and functionalization occur in a substantially simultaneous manner. All necessary reactants for the functionalization are present when polymerization is initiated. The nitrogen-containing functional group is provided as a part of a molecule having a release moiety which is preferably resonance stabilized or a tertiary alkyl type and which acts to aid the nitrogen-containing species in functioning as a leaving group.

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