物理性质
- 熔点−22 °C(文献)
- 沸点106.0±0.0 °C at 760 mmHg
- 闪点34.0±20.2 °C
- 密度1.4±0.1 g/cm3
- PSA:17.07
- LogP:0.69
- 折射率1.430
- 蒸汽压28.8±0.2 mmHg at 25°C
- 溶解性Miscible With Ethyl Ether, Acetone, Benzene And Carbon Tetrachloride.
- 敏感性易受潮
- 外观形态透明无色至微黄色液体
- 储存条件常温保存.
- 产品应用用于农药乐果,氟乙酰胺,医药,溶剂,致冷剂,灭火剂,助染剂,润滑油添加剂等的生产.氯乙酰氯用途广泛,仅除草剂就有3大系列40多个品种需消耗氯乙酰氯.
- 性质描述无色或微黄色液体,有强烈的刺激性,遇水分解.凝固点-22.5°C,沸点107°C(108-110°C),相对密度1.4202,折射率1.4530.能溶于苯,四氯化碳,醚和氯仿中.
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ECHA物质工作场所安全标识要求C&L通报REACH预注册废弃物危险特性清单上下游产品
CAS号79-11-8 氯乙酸 | CAS号463-51-4 乙烯酮 | CAS号75-44-5 光气 | CAS号98-07-7 三氯甲苯 | CAS号27843-27-2 1-Butene,2-chlo... | CAS号75-36-5 乙酰氯 | CAS号79-37-8 草酰氯 | CAS号541-88-8 氯乙酸酐 | CAS号110704-19-3 5-氯-2-(氯甲基)-1,3-苯并噻唑 | CAS号1115-24-8 N-氯乙酰基-DL-异亮氨酸 | CAS号108086-37-9 2-氯-n-(2-氯-5-硝基... | CAS号106700-04-3 2-chloro-N-(2-m... | CAS号109348-25-6 5-(chloromethyl... | CAS号107235-74-5 4-benzoyl-1-eth... | CAS号108441-34-5 2-chloro-N-[3-[... | CAS号109607-24-1 2-chloro-1-(4-m... | CAS号104246-27-7 2-氯-N-{4-[(1,3-... | CAS号111631-72-2 2-氯乙酰基-6,7-二甲氧基...合成工艺路线路线简述
- 合成目标产物 Chloroacetyl Chloride 主要起始原料 Acetyl Chloride
- (文献来源)合成步骤主要原料 Acetyl Chloride
乙烯酮置于二氧化硫,氯体系中,化学反应生成 氯乙酰氯
参考文献:Notes-Chloroacetyl Chloride From Ketene And Chlorine
标题:Notes-Chloroacetyl Chloride From Ketene And Chlorine
摘要:
DOI:10.1021/jo01095A638
海关参考信息
- 2903150000-1,2-二氯乙烷
2912110000-甲醛
2912120000-乙醛
2903110000-一氯甲烷及氯乙烷 - 💡 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-2004058888-A1
优先权日:2000-01-13
标题:Methods for synthesis of alpha-d-gal (1~>3) gal-containing oligosaccharides
发明人:BORNAGHI LAURENT; DEKANY GYULA; DRINNAN NICHOLAS BARRY; PAPAGEORGIOU JOHN; WEST MICHAEL LEO
摘要:This invention relates to reagents and methods for synthesis of biologically active di- and tri-saccharides comprising α-D-Gal(1→3)-D-Gal. In particular the invention provides novel reagents, intermediates and processes for the solution or solid phase synthesis of α-D-galactopyranosyl-(1→3)-D-galactose, and derivatives thereof. In one preferred embodiments the invention provides a protected monosaccharide building block of general formula (II): in which R 3 is methoxy or methyl; R 1 is H, benzoyl, pivaloyl, 4-chlorobenzoyl, acetyl, chloroacetyl, levulinoyl, 4-methylbenzoyl, benzyl, 3,4-methylenedioxybenzyl, 4-methoxybenzyl, 4-chlorobenzyl, 4-acetamidobenzyl, or 4-azidobenzyl; and R 2 is H, Fmoc, benzoyl, pivaloyl, 4-chlorobenzoyl, acetyl, chloroacetyl, levulinoyl, 4-methylbenzoyl, benzyl, 3,4-methylenedioxybenzyl, 4-methoxybenzyl, 4 -chlorobenzyl, 4-acetamidobenzyl, or 4-azidobenzyl.
专利号:WO-2025134140-A1
优先权日:2023-12-19
标题:A method for the synthesis of substituted anthranilic amide compounds, intermediates and salts thereof
发明人:MALVIYA NITIN JAIKANT; SINGH VIPENDER; SHAH JIGARKUMAR HARKISHANDAS; KALE MANOJ GANPAT; KAVITAKE SANTOSH GIRIDHAR; BORHADE AJIT SAHEBRAO; KLAUSENER ALEXANDER G M
权利人:PI INDUSTRIES LTD
摘要:The present invention discloses a method for the synthesis of compounds of formula (I) or a salt thereof, wherein, R is selected from hydrogen, halogen, cyano, C1-C12 alkyl, C1-C12 haloalkyl, C1-C12 alkoxy, C1-C12 haloalkoxy, or C3-C8 cycloalkyl; R4 is selected from hydrogen, C1-C12 alkyl, C2-C12 alkenyl, C2-C12 alkynyl, C1-C12 haloalkyl, C2-C12 haloalkenyl, C2-C12 haloalkynyl, C1-C12 alkoxy, C1-C12 haloalkoxy, C3-C8 cycloalkyl, or C3-C8 cycloalkyl-C1-C10 alkyl; and n represents an integer selected from 0-4. The method further comprises the synthesis of an anthranilic diamide compound of formula (A).
专利号:US-2023339906-A1
优先权日:2020-09-26
标 题 :A process for the synthesis of anthranilic acid/amide compounds and intermediates thereof
发明人:SYTHANA SURESH KUMAR; NAGLE PRAMOD; KUMAR VIJAY KUMAR; KANAWADE SHRIKANT BHAUSAHEB; CHANDRE TUKARAM NIVRUTTI; THUBE VINAYAK KISAN; PATIL PRADEEP PRAKASH; SHUKLA SHALINI; SHENDE KANTILAL BALU; PATRA PRANAB KUMAR; KLAUSENER ALEXANDER G M
权利人:PI INDUSTRIES LTD; PI INDUSTRIES LTD
摘要:The present invention discloses a process for the synthesis of compound of formula (VII) or a salt thereof,wherein, R, R1, R2, R3, R4a and R4b are as defined in the detailed description. The process further comprises the synthesis of an anthranilic diamide compound of formula (I).
专利号:WO-2024036115-A1
优先权日:2022-08-08
标题:Continuous flow synthesis of lorazepam
发明人:THOMPSON DAVID; BIYANI SHRUTI; HYUN SEOK-HEE; MCGUIRE MICHAEL
权利人:PURDUE RESEARCH FOUNDATION; CONTINUITY PHARMA LLC
摘要:A method for synthesis of Lorazepam in a continuous flow using continuous flow reactor, in which method comprises five steps including N-acylation, diazepine ring closure, imine N- oxidation, Polonovski-type rearrangement, and ester hydrolysis; a green reagent comprising a peroxide reagent and rhenium oxide catalyst for N-oxidation of delorazepam; and an ammonium source combination for the synthesis of delorazepam.
专利号:EP-2644590-A1
优先权日:2012-03-30
标 题:Synthesis of 2-(3,4-difluorophenyl)cyclopropanamine derivatives and salts
权利人:LEK PHARMACEUTICALS
摘要:The present invention relates to the field of organic synthesis and describes the synthesis of specific intermediates suitable for the preparation of triazolopyrimidine compounds such as ticagrelor.
专利号:US-9440940-B2
优先权日:2014-03-18
标 题:Methods for synthesis of psoralen derivatives
发明人:REFOUVELET BERNARD
权利人:MACOPHARMA S A S
摘要:Methods for the synthesis of psoralen derivatives are provided. In one embodiment, the method may include acetylating a compound of formula (II) to form a compound of formula (III), subjecting the compound of formula (III) to a Fries rearrangement to form a compound of formula (IV), and subjecting the compound of formula (IV) to cyclization, reduction and aromatization, to form a compound having the following formula (I):