CAS: 594-89-8; 1,1,1,2,2,3,3-Heptachloropropane

该化合物是一种属于氯化碳氢化合物类的合成有机化合物,其特点是结构复杂,有多种氯原子附着在丙烷脊柱上,这种化合物一般没有色素,可粉黄黄色液体,有明显的气味,以其稳定性和抗降解性为名,这助长了其在环境中的持久性. 1,1,1,2,2,2,3,3-七氯丙烷历来被用作杀虫剂和杀虫剂,尽管由于与氯化化合物有关的环境和健康问题,其使用有所减少,但被归类为潜在的环境污染物,接触可通过各种途径,包括吸入,摄取和皮肤接触,由于其毒理学特征,包括潜在的致癌影响,已实施管制措施,限制其使用,减轻其对人类健康和环境的影响.

结构式图片

相似化合物

3849-33-0 15600-01-8 21700-31-2

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

dichloroacethyl chloride 1,1,2,2-tetrachloroethylene chloroform pentachloroethane 1,1,2,2-tetrachloroethylene 1,2,3,3-tetrachloro-1,1,2-trifluoro-propane 1,1,2,2,3-pentachloro-3,3-difluoropropane 1,1,2,2,3,3-hexachloro-1-fluoro-propane

合成工艺路线路线简述

    📜五氯丙酮置于五氯化磷体系中,化学反应生成 1,1,1,2,2,3,3-七氯丙烷
    参考文献:Fritsch,Justus Liebigs Annalen Der Chemie,1897,Vol. 297,P. 314
    标题:Fritsch,Justus Liebigs Annalen Der Chemie,1897,Vol. 297,P. 314

    海关参考信息

    专利信息


    专利号:US-6235957-B1
    优先权日:1998-06-29
    标 题 :Process for the preparation of cyclopropylacetylene
    发明人:CHOUDHURY ANUSUYA
    权利人:DU PONT PHARM CO
    摘要:The present invention relates generally to novel methods for the synthesis of cyclopropylacetylene which is an essential reagent in the asymmetric synthesis of (S)-6-chloro-4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one; a useful human immunodeficiency virus (HIV) reverse transcriptase inhibitor.

    专利号:US-7833926-B2
    优先权日:2005-07-01
    标题 :Arylphenoxy catalyst system for producing ethylene homopolymer or copolymers of ethylene and α-olefins
    发明人:WOO TAE WOO; OK MYUNG AHN; HAHN JONG SOK; LEE MAL-OU; KANG SANG OOK; KO SUNG-BO; KIM TAE-JIN; KIM SUNG-KWAN
    权利人:SK ENERGY CO LTD
    摘要:The present invention relates to an arylphenoxy catalyst system producing an ethylene homopolymer or copolymers of ethylene and α-olefins, and a method of producing an ethylene homopolymer or copolymers of ethylene and α-olefins having a high molecular weight under a high temperature solution polymerization condition using the same. The catalyst system includes a group IV arylphenoxy-based transition metal catalyst and an aluminoxane cocatalyst or a boron compound cocatalyst. In the transition metal catalyst, a cyclopentadiene derivative and arylphenoxide as fixed ligands are located around the group IV transition metal, arylphenoxide is substituted with at least one aryl derivative and is located at the ortho position thereof, and the ligands are not crosslinked to each other. The catalyst includes an environmentally-friendly raw material, synthesis of the catalyst is economical, and thermal stability of the catalyst is excellent. It is useful for producing an ethylene homopolymer or copolymers of ethylene and α-olefins having various physical properties in commercial polymerization processes.

    专利号:WO-2025019747-A1
    优先权日:2023-07-20
    标题:Processes for the production of z-1,1,1,4,4,4-hexafluoro-2-butene intermediates and compositions thereof
    发明人:PENG SHENG
    权利人:CHEMOURS CO FC LLC
    摘要:Methods of synthesis of intermediates, such as 2-chloro-1,1,1,4,4,4-hexafluoro-2-butene and 2,3-dichloro-1,1,1,4,4,4-hexafluoro-2-butene, which can be used in the production fluorinated olefins, such as 1,1,1,4,4,4-hexafluoro-2-butene, from hexafluorobutadiene, are provided.

    专利号:US-5446211-A
    优先权日:1994-04-01
    标 题 :Chlorination of difluoromethyl methyl ether
    发明人:O'NEILL GERALD J; BULKA ROBERT J
    权利人:HAMPSHIRE CHEMICAL CORP
    摘要:The synthesis of fluorinated dimethyl ethers of the formula CF 2 HOCCl x F y H 3- (x+y) wherein x is 0, 1 or 2; y is 1, 2 or 3; and wherein (x+y) is 1, 2 or 3. The process involves chlorination of methyl difluoromethyl ether in the presence of a solvent to form a chlorinated reaction product of the formula CF 2 HOCH 3-z Cl z wherein z is 1, 2 or 3. The process may also be carried out in the presence of oxygen in order to inhibit the formation of CF 2 HOCCl 3 . The resulting compound(s) is then fluorinated with HF before or after separation, to give a fluorinated reaction product including the aforementioned fluorinated dimethyl ethers.

    专利号:US-6586615-B1
    优先权日:2001-01-10
    标题:α-aminoboronic acids prepared by novel synthetic methods
    发明人:KETTNER CHARLES A; JAGANNATHAN SHARADA; FORSYTH TIMOTHY PATRICK
    权利人:BRISTOL MYERS SQUIBB CO
    摘要:The present invention relates to a novel class of alpha-aminoboronic acids of Formula (V),which are useful as intermediates in synthetic processes for inhibitors of the serine proteases, leukocyte elastase, pancreatic elastase, cathepsin G, and chymotrypsin. More specifically, the alpha-aminoboronic acids are useful as intermediates for the synthesis of Hepatitis C Virus (HCV) protease inhibitors. This invention also generally relates to novel methods for the preparation of alpha-aminoboronic acids.

    专利号:EP-3070087-B1
    优先权日:2011-08-05
    标题 :Intermediates for the synthesis of cyclic p1 linkers as factor xia inhibitors

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Drabowicz, J.; Lewkowski, J.; Stevens, C. V.; Krasowska, D.; Karpowicz, R., Science of Synthesis, (2009) 42, 640.
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