物理性质
- 熔点−64(文献)
- 沸点40.3±3.0 °C at 760 mmHg
- 闪点7.8±10.7 °C
- 密度2.2±0.1 g/cm3
- PH:5.2 (H2O, 25°C)
- LogP:1.5
- 折射率1.528
- 蒸汽压437.1±0.1 mmHg at 25°C
- 溶解性Water: Soluble14G/l At 20°c
- 敏感性光敏感
- 外观形态透明液体
- 储存条件2-8°C
- 产品应用用于医药,有机合成,吡啶的检验,显微镜检查等.
- 性质描述无色易燃体.熔点-66.45°C,沸点42.4°C,相对密度2.279(20/4°C),折光率1.5317.能与乙醇,乙醚混溶,溶于丙酮和苯,微溶于水.见光变红色.
欧盟法规
统一分类与标签压力设备指令-第1组危险流体REACH注册ECHA物质工作场所安全标识要求食品接触材料-禁用CMR物质化妆品禁用物质清单ECHA物质C&L通报REACH预注册废弃物危险特性清单上下游产品
CAS号75-77-4 三甲基氯硅烷 | CAS号5927-18-4 三甲基膦酰基乙酸酯 | CAS号1125-88-8 苯甲醛二甲缩醛 | CAS号4461-87-4 1,1-二甲氧基丁烷 | CAS号311-46-6 乙基膦酰基乙酸二甲酯 | CAS号933-40-4 1,1-二甲氧基环己烷 | CAS号29238-81-1 dimethyl trichl... | CAS号62327-21-3 P,P-二甲基膦酰乙酸叔丁酯 | CAS号16965-84-7 [dimethoxyphosp... | CAS号1015-28-7 2-dimethoxyphos... | CAS号108903-57-7 trimethyl-[2-me... | CAS号109561-74-2 6-methyl-5,7-di... | CAS号111238-14-3 methyl 2-(2,2-d... | CAS号105020-38-0 1-甲基-1,2,3-三氮唑-... | CAS号105020-39-1 2-甲基-1,2,3-三氮唑-... | CAS号57362-82-0 1-甲基-1,2,3-三氮唑-... | CAS号105285-61-8 2-[1-(benzenesu... | CAS号10493-37-5 邻甲氧基苯丙醇 | CAS号105889-17-6 6-(4-methoxyphe... | CAS号108460-23-7 7-methyl-4H-thi...氯甲烷置于甲醇,Sodium Iodide体系中,化学反应生成 碘甲烷
参考文献:无机汞和甲基汞对虾虾直接和直接营养污染的同时实验研究
标题:无机汞和甲基汞对虾虾直接和直接营养污染的同时实验研究
摘要:进行了一项实验研究,以调查无机汞(hg(II))或甲基汞(mehg)对小龙虾astacus Astacus的直接和直接加营养污染途径.直接暴露基于低污染条件,溶解相中分别为 300 和 30 Ng/l,在 20 摄氏度下持续 30 天.营养暴露基于每天食用亚洲蛤蜊 Corbicula Fluminea,之前在 40 天被污染类似的暴露条件.双壳贝类中的 Hg 浓度非常相似:Hg(II) 为 1,451 +/-287 Ng/g,Mehg 为 1,346 +/-143 Ng/g.在甲壳类动物中,在暴露 15 天和 30 天后,在整个生物体水平和八个器官(鳃,胃,肠,肝胰腺,尾肌,绿腺,甲壳和血淋巴)中分析了汞的生物蓄积.结果分析表明,Hg(II) 和 Mehg 积累有利于 Mehg 的显着差异:对于直接路线,金属浓度之间的比率接近 8;对于营养途径,即使直接加营养污染途径中的 Hg 浓度与
DOI:10.1002/etc.5620200609
专利信息
专利号:US-11667658-B2
优先权日:2021-06-30
标 题:Chemical synthesis of the organoarsenical antibiotic arsinothricin
发明人:ROSEN BARRY P; YOSHINAGA MASAFUMI; WNUK STANISLAW F; HOWLADER MD ABU HASAN; SUZOL SK MD SAZZAD HOSSAIN
权利人:ROSEN BARRY P; YOSHINAGA MASAFUMI; WNUK STANISLAW F; HOWLADER MD ABU HASAN; SUZOL SK MD SAZZAD HOSSAIN; THE FLORIDA INTERNATIONAL UNIV BOARD OF TRUSTEES
摘要:The subject invention provides methods for the chemical synthesis of racemic arsinothricin (D,L-AST), the novel organoarsenical antibiotic. One is by condensation of the 2-chloroethyl(methyl)arsinic acid with acetamidomalonate, and the second involves reduction of the N-acetyl-protected derivative of hydroxyarsinothricin (AST-OH) and subsequent methylation of the resulting sodium salt of trivalent arsenic intermediate with methyl iodide. The enzyme AST N-acetyltransferase (ArsN1) was utilized to purify L-AST from racemic AST. This expedient chemical synthesis of AST provides a source of this novel antibiotic for future drug development.
专利号:WO-2021014395-A1
优先权日:2019-07-24
标题:Process for the synthesis of deuterated capsaicin, capsaicinoids and synthetic capsaicin analogs
发明人:ORUGANTI SRINIVAS; AMRUTAPU SRAVANTH KUMAR; SAMPATH MAGESH; SEN SAIKAT
权利人:DR REDDY’S INST OF LIFE SCIENCES
摘要:The present application provides novel processes for the synthesis of deuterated intermediates of capsaicinoids, particularly II, III, IV and V of capsaicinoids, relating to pharmaceutical applications. The invention also provides novel intermediates of compounds of formula IX, XIV, XV, XVI, XVII, XVIII, XX and XXI utilized in the process of making deuterated capsaicin II, III, IV and V.
专利号:US-2019047933-A1
优先权日:2016-03-15
标 题:Process for the synthesis of (2e, 4e, 6z, 8e)-8-(3,4-dihydronaphthalen-1(2h)-ylidene)-3,7-dimethylocta-2, 4, 6-trienoic acid
发明人:ABEL ULRICH; RÉPÃ?SI JÓZSEF; Szabó András; SZÜCSNÉ CSERÉPI STEFÃ?NIA; Bor Ã?dám
权利人:ABEL ULRICH; REPASI JOZSEF; SZABO ANDRAS; SZUECSNE CSEREPI STEFANIA; BOR ADAM; BRICKELL BIOTECH INC
摘要:This invention relates to a novel method for the synthesis of (2E,4E,6Z,8E)-8-(3,4-dihydronaphthalen-1(2H)-ylidene)-3,7-dimethylocta-2,4,6-trienoic acid. In particular, the invention relates to several improvements in several individual steps of the multi-step synthesis scheme
专利号:US-9126995-B2
优先权日:2011-11-08
标题:Method for catalytic asymmetric synthesis of optically active isoxazoline compound and optically active isoxazoline compound
发明人:TOYAMA KEN-ICHI; MORIYAMA YUJI; MATOBA KAZUTAKA; YAOSAKA MANABU; IKEDA EITATSU
权利人:NISSAN CHEMICAL IND LTD
摘要:There is provided a method for catalytic asymmetric synthesis of optically active isoxazoline compound and an optically active isoxazoline compound. A method for catalytic asymmetric synthesis of optically active isoxazoline compound of a formula (6) including reacting an α,β-unsaturated carbonyl compound of a formula (1) and a hydroxylamine in a solvent in the presence of a base by adding a chiral phase transfer catalyst. An optically active isoxazoline compound of a formula (13) that can be synthesized by the method.
专利号:US-5200516-A
优先权日:1990-02-16
标 题:Synthesis of sugars from substituted and unsubstituted arene diols
发明人:HUDLICKY TOMAS
权利人:VIRGINIA TECH INTELL PROP
摘要:There are disclosed processes for the synthesis of substituted and unsubstituted arene diols useful in the further synthesis of sugars, sugar derivatives, chiral synthons or amino acids.
专利号:US-4226770-A
优先权日:1978-02-10
标题:Synthesis of steroids
发明人:KAISER EMIL T
权利人:KAISER EMIL T
摘要:The synthesis of 1α,25-dihydroxycholesterol, 1α,25-dihydroxy-7-dehydrocholesterol and 1α,25-dihydroxycholecalciferol and other sterol derivatives from bile acids. Also the synthesis of 3,6-diketo steroids useful in the production of 1α,25-dihydroxycholesterol and other sterols which are biologically active or can be converted to biologically active sterols. The invention involves the sterols so produced and the processes by which they are prepared.