- 英文名称1,1,1,2,2,3,3-Heptachloropropane
- 中文名称1,1,1,2,2,3,3-七氯丙烷
- IUPAC名称1,1,1,2,2,3,3-heptachloropropane
- 其它别名1,1,1,2,2,3,3-氯丙烷; Unsym-Heptachloropropane
- CAS编号594-89-8
- MFCD编号:MFCD00000847
- EINECS号:209-856-1
- FDA UNII编号:J7BW4GD9PS
- 分子式:C3HCl7分子量:285.21
- 产品CID: 1571708
- 产品分类有机原料→分子砌块→脂肪链类化合物
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 📜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
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