物理性质
- 熔点246-256 °C
- 沸点448.0±0.0 °C at 760 mmHg
- 闪点209.1±13.7 °C
- 密度1.2±0.1 g/cm3
- PSA:0.0
- LogP:5.91
- 折射率1.771
- 蒸汽压0.0±0.5 mmHg at 25°C
- 溶解性<0.0001克/升
- 敏感性1.易燃、有毒,防止皮肤接触。2.本品有毒,防止皮肤直接接触和吸入蒸气。车间应有良好通风,设备应密闭,操作人员应穿戴防护用具。3. IARC致癌性评估:有限证据,引发活性,与正十二烷同时存在时增强活性。
- 外观形态无色至米色晶体或粉末
- 储存条件本品可燃,应贮于阴凉通风仓库内,瓶装。
- 产品应用用于非磁性金属表面探伤用荧光剂,化学仪器紫外线过滤剂,光敏剂及照像感光剂,用于染料生产,代替洗油作农药敌稗的溶剂和增效剂.
- 性质描述白色或带银灰色,黄绿色鳞片状或平斜方八面结晶体,在苯中结成无色斜方片晶,在紫外线下有紫色荧光.可燃.有毒.真空中易升华.熔点255°C,沸点440.7°C,相对密度1.274.微溶于醇,醚,二硫化碳和冰醋酸,在25°C时1g能溶于1300ml无水乙醇,480ml甲苯,在100°C时在甲苯中约溶解5,略溶于沸苯,不溶于水.
欧盟法规
[统一分类与标签ECHA物质工作场所安全标识要求ECHA物质化妆品禁用物质清单食品接触材料-禁用CMR物质C&L通报REACH预注册欧盟候选物质清单废弃物危险特性清单上下游产品
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参考文献:Thermal Stability,Crystallization Kinetics,And Grain Growth In An Amorphous Al85Ce5Ni8Co2 Alloy
标题:Thermal Stability,Crystallization Kinetics,And Grain Growth In An Amorphous Al85Ce5Ni8Co2 Alloy
摘要:通过 X 射线衍射和差示扫描量热法(dsc)研究了熔淬无定形 Al85Ce5Ni8Co2 合金的热稳定性和结晶动力学.玻璃化转变之后是过冷液态区(21 oc),然后是两步结晶过程.最终的微观结构包含 Al3Ce,α-Al,Al3Ni 和 Al9Co2 相.在 275-285 oc 范围内对淬火样品进行的等温退火表明,两个结晶反应都是通过成核和生长过程发生的.为了研究材料的结晶动力学和稳定性,还在预退火后进行了不同时间的连续加热 Dsc 测量.对等温 Dsc 曲线进行的 Avrami 分析表明,随着退火温度的升高,三维成核和生长过程变得更加主要.平均比晶界能量与高角度晶界相对应,表明存在独立的成核事件.
Doi:10.1557/jmr.2002.0315
专利信息
专利号:US-9353057-B2
优先权日:2003-12-30
标 题:Synthesis of acyloxyalkyl carbamate prodrugs and intermediates thereof
发明人:GALLOP MARK A; DAI XUEDONG; SCHEUERMAN RANDALL A; RAILLARD STEPHEN P; MANTHATI SURESH K; YAO FENMEI; PHAN THU; LUDWIKOW MARIA; PENG GE; BHAT SEEMA
权利人:XENOPORT INC
摘要:Methods for synthesis of 1-(acyloxy)-alkyl carbamates, particularly, the synthesis of 1-(acyloxy)-alkyl carbamate prodrugs of primary or secondary amine-containing drugs are described. Also described are methods for synthesis of 1-(acyloxy)-alkyl N-hydroxysuccinimidyl carbonates which are useful intermediates in the synthesis of 1-(acyloxy)-alkyl carbamates are also described.
专利号:US-6770436-B1
优先权日:1996-11-14
标题:Chemical amplification for the synthesis of patterned arrays
发明人:BEECHER JODY E; GOLDBERG MARTIN J; MCGALL GLENN H
权利人:AFFYMETRIX INC
摘要:Radiation-activated catalysts (RACs), autocatalytic reactions, and protective groups are employed to achieve a highly sensitive, high resolution, radiation directed combinatorial synthesis of pattern arrays of diverse polymers. When irradiated, RACs produce catalysts that can react with enhancers, such as those involved in autocatalytic reactions. The autocatalytic reactions produce at least one product that removes protecting groups from synthesis intermediates. This invention has a wide variety of applications and is particularly useful for the solid phase combinatorial synthesis of polymers.
专利号:US-10711138-B2
优先权日:2016-04-08
标题:Intermediates and procedures for the synthesis of functional materials
发明人:KIRSCH PEER; GUNST SUSANN
权利人:MERCK PATENT GMBH
摘要:The present invention relates to heteroaromatic compounds which have two different reactive groups, their use in the synthesis of asymmetrically substituted compounds, and synthesis processes in which the compounds according to the invention are reacted sequentially with two different compounds, whereby an asymmetrically substituted compound is formed.
专利号:US-2003162992-A1
优先权日:2001-12-14
标 题 :Preparation of intermediates useful in the synthesis of antiviral nucleosides
发明人:WATANABE KYOICHI A; DU JINFA
摘要:The present invention is an efficient process for the manufacture of α-acyloxyacetaldehyde, a key intermediate in the synthesis of 1,3-oxathiolane and 1,3-dioxolane nucleosides.
专利号:US-2010087658-A1
优先权日:1996-08-06
标 题 :Methods and intermediates for synthesis of selective dpp-iv inhibitors
发明人:CAMPBELL DAVID ALAN; LEITAO EMILIA P T; WU ZHEN-PING; WANG PENG
权利人:PHENOMIX CORP
摘要:Methods and intermediates for the synthesis of selective inhibitors of dipeptidyl peptidase IV (DPP-IV) are provided. Coupling of a carboxylate salt with a boro-proline derivative provides a protected form of a DPP-IV inhibitor, which may be deblocked to yield the medicinal compound. The carboxylate salt can be a crystalline form of a sodium salt or a dicyclohexylammonium salt. The inhibitor can be used in the treatment of diabetes.
专利号:US-10918627-B2
优先权日:2016-05-11
标 题:Convergent and enantioselective total synthesis of Communesin analogs
发明人:MOVASSAGHI MOHAMMAD; LATHROP STEPHEN PAUL; POMPEO MATTHEW W; CHANG WEN-TAU TIMOTHY
权利人:MASSACHUSETTS INST TECHNOLOGY
摘要:A highly convergent biomimetic synthesis of a complex polycyclic scaffold has been successfully implemented. From these efforts, compounds having a structure of Formula (I): n nor a pharmaceutically acceptable salt, tautomer or stereoisomer thereof, wherein R 1 -R 8 and m, n, r, s, t, and u are as defined herein, is provided. Methods of making such compounds are also disclosed as are methods for the treatment of cancer, various infectious diseases, and abnormal cardiovascular function.