- ⚠️危险化学品目录(2015年版) 特异性靶器官毒性-一次接触,类别3(呼吸道刺激、麻醉效应)
- 英文名称1,1,2-Trichlorotrifluoroethane
- 中文名称1,1,2-三氯三氟乙烷(CFC-113)
- IUPAC名称1,1,2-trichloro-1,2,2-trifluoroethane
- 其它别名1,1,2-Trichloro-1,2,2-trifluroethane
- CAS编号76-13-1
- MFCD编号:MFCD00000782
- EINECS号:200-936-1
- FDA UNII编号:0739N04X3A
- 分子式:C2Cl3F3Lewis structure
- 分子量:187.38
- 产品CID: 1753128
- 产品分类有机原料 → 有机卤素化合物 → 卤代烷
物理性质
- 熔点-35.0 °C
- 沸点47.7 °C
- 闪点195 °C
- 密度1.5635 g/cu cm at 25 °C
- PSA:0.0
- LogP:2.9189
- 折射率n20/D 1.358(文献)
- 蒸汽压363 mm Hg at 25 °C
- 溶解性In water, 170 mg/L at 25 °C
- 敏感性1,1,2-TRICHLORO-1,2,2-TRIFLUOROETHANE yields violent reactions with Al, Ba, Li, Sm, Na/K alloy and Ti (NTP, 1992). May react exothermically with aluminum.
- 外观形态澄清无色无色气体挥发性液体.
- 储存条件储存于阴凉,通风的库房.远离火种,热源,并应与活性金属粉末等分开存放,切忌混储.储区应备有泄漏应急处理设备和合适的收容材料. 用敞口容器存放时,需加水密封.使用240L铁桶包装,每桶重200kg.不可直接接触火焰,按危险品规定贮运.
- 产品应用用作聚三氟氯乙烯单体,也用作致冷剂,清洗剂,干洗剂,发泡剂,灭火剂和溶剂等.
MSDS等安全信息
- GHS象形图


- GHS符号GHS07 & GHS09;
注释: Exclamation mark & Environment - 危险类别严重眼刺激 类别2
水生慢性毒性 类别2
Ozone 1 - 警示词Warning(警告)
- 危险描述H319 |造成严重眼刺激.
H411 |对水生生物有毒并具有长期持续影响.
H420 |破坏高层大气中的臭氧,危害公众健康和环境
EUH059 |Hazardous to the ozone layer. - 防范说明P260, P261, P264, P270, P271, P304+P340, P319, P332+P317, P403+P233, P405, and P501
- UN编号3082.0
- 危险品标志N
- 安全声明S36/37,S45,S59,S61
- 危险类别码R52/53,R59
- WGK Germany2
欧盟法规
ECHA物质ECHA物质C&L通报REACH预注册上下游产品
1,1,2,2-tetrachloroethylene 1,1-difluorotetrachloroethane 1,1,1,2-tetrachoroethane 1,1,1-trichloro-2,2-difluoroethane 1,1-difluorotetrachloroethane hexachloroethane 1,1,2-Trifluoroethan trichlorofluoromethane四氯乙烯置于氟化锆,氢氟酸体系中,化学反应生成 1,1,2-三氯三氟乙烷(cfc-113)
参考文献:Manufacture Of 1,2,2-Trichloro-1,1,2-Trifluoroethane
标题:Manufacture Of 1,2,2-Trichloro-1,1,2-Trifluoroethane
专利信息
专利号:US-11548898-B2
优先权日:2017-07-06
标题 :Synthesis of halichondrins
发明人:KISHI YOSHITO; AI YANRAN; YE NING; WANG QIAOYI; YAHATA KENZO; ISO Kentaro; NAINI SANTHOSH REDDY; YAMASHITA SHUJI; LEE JIHOON; OHASHI ISAO; FUKUYAMA TAKASHI
权利人:HARVARD COLLEGE; EISAI R&D MAN CO LTD
摘要:The present invention provides methods for the synthesis of ketones involving a Ni/Zr-mediated coupling reaction. The Ni/Zr-mediated ketolization reactions can be used in the synthesis of halichondrins (e.g., halichondrin A, B, C; homohalichondrin A, B, C; norhalichondrin A, B, C), and analogs thereof. Therefore, the present invention also provides synthetic methods useful for the synthesis of halichondrins, and analogs thereof. Also provided herein are compounds (i.e., intermediates) useful in the synthesis of halichondrins, and analogs thereof. In particular, the present invention provides methods and compounds useful in the synthesis of compound of Formula (H3-A).
专利号:US-2022372000-A1
优先权日:2021-05-05
标 题:New Process for the Synthesis of 5-Fluoro-3-(Difuoromethyl)-5-Fluoro-1-Methyl-1H-Pyrazole-4-Carboxylic Acid Derivatives and the Free Acid Thereof
发明人:LUO WEIFEN; WU WENTING
权利人:FUJIAN YONGJING TECH CO LTD
摘要:The invention provides a new process for the synthesis of 5-fluoro-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid derivatives and the free acid thereof, involving a direct fluorination reaction with a fluorination gas comprising or consisting of elemental fluorine (F2), in a reactor which is resistant to elemental fluorine (F2) and hydrogen fluoride (HF), and wherein in the process as a starting material a difluoromethyl-pyrazole compound dissolved in an inert solvent is subjected to the direct fluorination reaction. Some particular examples of 5-fluoro-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid derivatives which can be prepared according to the process of the invention are 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid fluoride (5F-DFMPAF), also known under the alternative name 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carbonyl fluoride; 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid ethylester (5F-DFMP); and 3-(chlorodifluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid ethylester (5F-CDFMP), or the corresponding methyl esters. The 5-fluoro-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid can be obtained from its carboxylic acid derivatives such as, e.g., mentioned before in that the acid derivative is converted to the corresponding carboxylic acid.
专利号:US-10973847-B2
优先权日:2017-06-30
标题 :Core-to-surface polymerization for the synthesis of star polymers and uses thereof
发明人:JOHNSON JEREMIAH A; GOLDER MATTHEW R
权利人:MASSACHUSETTS INST TECHNOLOGY
摘要:Disclosed are methods, compositions, reagents, systems, and kits to prepare star polymers, as well as compositions and uses thereof. Various embodiments show that synthesis of these polymers contain low metal concentration to provide polymers for diverse biomedical applications including in vivo applications.
专利号:US-12221452-B2
优先权日:2017-10-04
标题:Synthesis of cantharidin
发明人:DAVIDSON MATTHEW GENE; EKLOV BRIAN MATTHEW; WUTS PETER; LOERTSCHER BRAD MELVIN; SCHOW STEVEN R
权利人:VERRICA PHARMACEUTICALS INC
摘要:The invention provides synthetic methods for the preparation of cantharidin and analogs thereof. In one aspect, the invention provides an improved Diels-Alder cycloaddition to generate a key intermediate en route to cantharidin and analogs thereof. In certain embodiments, the new Diels-Alder reaction involves reacting Compound (2) in the presence of furan, and in the absence of acid or increased pressure, in an aprotic polar solvent with slight warming, to yield Compound (1) in favorable yield and exo-endo ratio. In another aspect, the invention also provides a new Diels-Alder reaction between compounds of Formula (III) and furan to yield compounds of Formula (IV), which can then be transformed into cantharidin or analogs thereof. In yet another aspect, the invention describes a new palladium-mediated carbonylation providing another key intermediate en route to cantharidin and analogs thereof. In addition to synthetic methods, present invention also provides compounds (i.e., intermediates) useful in the synthesis of cantharidin and analogs thereof. Compounds provided herein may have biological activity, and therefore may be used in the treatment of diseases or conditions (e.g., infectious diseases and skin conditions).
专利号:US-4219489-A
优先权日:1978-09-05
标题:Synthesis of steroids
发明人:BUNES LEONARD A; JOHNSON WILLIAM S
权利人:STANFORD LELAND JUNIOR UNIV TR
摘要:Method and compounds are provided for use in the synthesis of steroids wherein a polyolefin is provided having an initiating group having a chalcogen atom in juxtaposition to a double bond, so as to be capable of bond formation to close to form a ring and having a terminating group involving pi unsaturation (a double or triple bond) conjugated to an aromatic ring. Upon acid catalysis, sigma bonds are formed through the interaction of a carbocation formed at the carbon atom bonded to the chalcogen atom and the double bond intermediate the initiating group and the terminating group, which close to form rings of a steroid nucleus, the carbocation interacting with the pi unsaturation conjugated with the aromatic group and being captured by a nucleophile present in the acidic reaction medium. The resulting steroid product may then be modified in known ways to produce known steroids.
专利号:US-4756739-A
优先权日:1985-12-21
标题 :Pyridine derivatives and the N-oxides thereof, and the use thereof as intermediates for the synthesis of plant protecting agents
发明人:FUSS ANDREAS; KOCH VOLKER
权利人:HOECHST AG
摘要:The compounds of the formula I (I) in which A denotes N or N->O, Z denotes O or NH, R denotes H, (halo)alkyl, (halo)alkenyl, (halo)alkynyl or alkoxycarbonyl, R1 denotes hydrogen, halogen, amino, -NHOH, hydroxyl, (substituted) phenylazo or a radical of the formulae Y=C=N-, Y1Y2C=N-, Y3NH- or K denotes 0 or 1, and m and n, independently of one another, denote a number from 1 to 4, with the proviso that, when Z-R denotes OH or NH2, (R1)n denotes at least one radical of the formula or represents two radicals, in the 5 or 6 position of the heterocyclic ring, which, in the 5 position, denote halogen and, in the 6 position, denote a radical of the group comprising halogen, amino, hydroxyl or phenylazo, which may be substituted as specified above, are valuable intermediates in the synthesis of plant protection agents.