Metallocene Catalysts & Life Science Technologies von MCat GmbH

Katalog: Metallocene Catalysts & Life Science Technologies
Unternehmen: MCat GmbH

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3 cl 32 n 5 cl 54 cl 95 n active br c 1 n c 220 c 96 c h 21 cl cl 500 cl 75 et 1 32 et 300 et 40 et 54 et 55 et 900 f 280 f 500 fep fw 7 g 40 hf j 130 light lithium mc mc 19 mc 5 2 mc 55 mc 55 1 mg mg 34 mg f p 250 p 35 page 22 page 69 r 900 s 320 s 450 s 67 si si 12 tetra titanium tris type a zr zr 15 zr 7 zr 7 s

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mc 8402 dichloro[1,1 bis diphenylphosphino ferrocene cadmiumii c h cl cdfep 34 28 2 2 fw 737.70 1g 2g 230 320 hafnium mc 8592 tris-neopentylhafnium iv chloride c h clhf fw 427.37 15 33 air moisture and light sensitive storage temperature minus 80°c 500 mg 2g mc 8590 tetrabenzylhafniumiv c h hf fw 543.02 28 28 160 380 98 air moisture and light sensitive storage temperature minus 30°c 1g 2g mc 8591 tetraneopentylhafniumiv c h hf fw 463.06 20 44 290 490 air moisture and light sensitive storage temperature minus 80°c 1g 2g mc 8510 bis butylcyclopenta-dienyl dichlorohafnium iv c h cl hf fw 491.80 18 26 2 420 700 500 mg 2g 60 130 page 4/35


mc 7019 >new 1,5,6,7-tetrahydro 2-methyl-3-phenyl-sindacenyllithium [210286-48-9 c h li fw 246.35 19 17 air and moisture sensitive 500 mg 1g 180 290 ligands mc 8562 >new s 2,2 bis diphenylphosphino 1,1 binaphthyl [76189-56-5 c h p 44 32 2 99 fw 622.69 250 mg 1g 5g 28 90 390 mc 8550 2,3-bis 2,6-di-isopropylphenyliminobutane c h n 28 40 2 fw 404.64 ligand used in the synthesis of a new family of highly active nickel and palladium catalysts for the polymerisation of ethylene and olefins m brookhart et al j am chem soc 1995 117 6414 m brookhart et al organometallics 1997 16 2005 500 mg 2g mc 8560 >new rac-2,2 bis diphenylphosphino 1,1 binaphthyl [98327-87-8 c h p 44 32 2 36 120 98 fw 622.69 1g 5g 25 g 29 96 420 mc 8561 >new r 2,2 bis diphenylphosphino 1,1 binaphthyl [76189-55-4 c h p 44 32 2 99 fw 622.69 250 mg 1g 5g 28 90 390 page 8/35


mc 9042 1h-2-methylindenyl-1-trimethylsilane c h si fw 202.37 13 18 98 1g 5g mc 9011 1,2,3,4,5-pentamethylcyclopentadiene [4045-44-7 c h 10 16 110 320 95 fw 136.24 1g 5g 25 g 22 90 410 mc 9044 1,2,3,4,5-pentamethyl-2,4-cyclopentadiene-1-yl trimethylsilane [87778-95-8 c h si fw 208.42 13 24 97 nd20 1.4880 d 0.864 1g 5g mc 9010 1,2,3,4-tetramethylcyclopentadiene [4249-10-9 c h 9 14 55 180 95 fw 122.21 mixture of isomers nd 20 1.4720 d 0.808 1g 5g mc 9043 2,3,4,5-tetramethyl-2,4-cyclopentadiene-1-yl trimethylsilane [134695-74-2 c h si fw 194.40 12 22 60 190 nd20 1.4860 d 0.852 1g 5g 100 350 page 11/35


mc 9081 >new 2-methyl-4-thiazolecarboxaldehyde [20949-84-2 c h nos fw 127.18 5 5 1g 5g mc 9094 >new 2,3,4,7,8,9,10,12-octahydro 1,1,4,4,7,7,10,10-octamethyl-1h-dibenzo b,h]fluorene [77308-48-6 c h 29 38 80 320 fw 386.62 1g 10 g 80 500 mc 9090 >new 1-phenylindene [1961-96-2 c h 98 fw 192.26 1g 5g 100 400 15 12 mc 9092 >new 2-phenylindene [4505-48-0 c h 98 fw 192.26 5g 120 15 12 mc 9093 >new 7-phenyl-indene [78383-19-4 c h 98 fw 192.26 1g 5g 100 400 15 12 mc 9096 >new 1,2,3,5-tetrahydro-6 methyl-s-indacen [202667-45-6 c h 13 14 fw 170.26 500 mg 1g 150 250 page 14/35


titanium mc 1401 r biphenyl 3,4-dimethyl-1-cyclopentadienyl titaniumiv r 1,1 binaphthyl-2 c h o ti fw 668.67 46 36 2 100 mg 500 mg mc 1402 s biphenyl 3,4-dimethyl-1-cyclopentadienyl titaniumiv s 1,1 binaphthyl-2 c h o ti fw 668.67 46 36 2 100 900 100 mg 500 mg mc 1020 bis cyclopentadienylchlorotitaniumiii dimer c h cl ti 20 20 2 2 230 900 fw 427.04 reagent for the rapid preparation of protected glycals j schwartz et al j org chem 1999 64 3987 1g 5g mc 1001 bis cyclopentadienyl difluoro-titaniumiv c h f ti fw 216.07 10 10 2 82 285 catalyst for the conversion of lactones into cyclic ethers 1g 5g 80 280 page 17/35


mc 1150 bis methylcyclopentadienyl difluorotitanium iv [1270-98-0 c h cl ti fw 219.36 5 5 3 97 moisture sensitive 1g 5g mc 1302 dichloro s,s ethylenebis 4,5,6,7-tetrahydro-1-indenyl titaniumiv [83462-46-8 c h cl ti fw 383.20 20 24 2 50 180 100 mg 500 mg mc 1305 rac-ethylenebis 4,5,6,7-tetrahydro-1 indenyl difluoro-titaniumiv c h f ti fw 350.29 20 24 2 72 300 100 mg 500 mg mc 1306 r,r ethylenebis 4,5,6,7-tetrahydro-1 indenyl difluoro-titaniumiv [214361-86-1 c h f ti fw 350.29 20 24 2 80 280 precatalyst for the highly enantioselective imine hydrosilylation s l buchwald et al j am chem soc 1996 118 6784 s l buchwald et al angew chem 1998 110 1174 100 mg 500 mg mc 1307 s,s ethylenebis 4,5,6,7-tetrahydro-1 indenyl difluoro-titaniumiv [178177-04-3 c h f ti fw 350.29 20 24 2 100 400 100 mg 500 mg 100 400 page 20/35


mc 1800 tetrabenzyl-titanium iv c h ti fw 412.41 28 28 air moisture and light sensitive storage temperature minus 30°c 1g 5g mc 1801 tetraneopentyl-titanium iv c h ti fw 332.45 20 44 240 540 air moisture and light sensitive storage temperature minus 80°c 1g 5g mc 1100 tetrachlorobis tetrahydrofuran titaniumiv [31011-57-1 c h cl o ti fw 333.91 8 16 4 2 350 990 10 g 100 g mc 1806 tris-benzyl-titanium iv chloride c h clti fw 356.73 21 21 26 130 air moisture and light sensitive storage temperature minus 80°c 500 mg 2g 250 690 page 23/35


mc 2150 bis cyclopentadienyl zirconiumiv tertbutylsulfonate hydride c h o szr fw 359.60 14 20 3 selective schwartz s type of reagent for the hydrozirconation of styrene g a luinstra dozententagung oldenburg 1999 100 mg 500 mg mc 2151 bis cyclopentadienyl zirconiumiv hydrido triflate chfo szr fw 371.49 11 11 3 3 390 900 soluble type of schwartz s reagent g a luinstra et al organometallics 1995 14 1551 k suzuki et al angew chem 1997 109 2578 j w sung et al j chem soc perkin trans 1997 1 591 j dupont et al tetrahedron asymmetry 1998 9 949 s harada et al tetrahedron 1998 54 753 100 mg 500 mg mc 2005 bis 1,3-dimethylcyclopentadienyl zirconiumiv dichloride [119445-92-0 c h cl zr fw 348.42 14 18 2 290 750 500 mg 2g mc 2003 bis methylcyclopentadienyl dichlorozirconiumiv [12109-76-1 c h cl zr fw 320.37 12 14 2 220 600 1g 5g mc 2802 tris-neopentylzirconium iv chloride c h clzr fw 340.10 15 33 70 220 500 mg 2g 340 770 page 26/35


mc 2311 rac-ethylenebis 4,5,6,7-tetrahydro-1-indenyl zirconiumiv 1,1 binaphthyl-2 c h o zr fw 639.95 40 36 2 100 mg 500 mg mc 2312 r,r ethylenebis 4,5,6,7-tetrahydro-1-indenyl zirconiumiv r 1,1 binaphthyl-2 [123236-85-1 c h o zr fw 639.95 40 36 2 170 450 asymmetric catalyst for the kinetic resolution of cyclic allylic ethers a h hoveyda et al j am chem soc 1996 118 3779 100 mg 500 mg mc 2313 s,s ethylenebis 4,5,6,7-tetrahydro-1-indenyl zirconiumiv s 1,1 binaphthyl-2 [132881-66-4 c h o zr fw 639.95 40 36 2 62 190 100 mg 500 mg mc 2800 tetra-benzyl-zirconium iv 28 28 62 190 98 [24356-01-2 c h zr fw 455.41 air moisture and light sensitive storage temperature minus 30°c 1g 5g mc 2803 tetra-benzyl-zirconium iv 28 28 190 620 95 [24356-01-2 c h zr fw 455 41 air moisture and light sensitive storage temperature minus 30°c 1g 5g 110 420 page 29/35


mc 7005 indenyllithium c h li fw 122.10 48.00125 9 7 air and moisture sensitive 1g 5g mc 7006 2-methylindenyllithium c h li fw 136.12 86.00125 10 9 60 240 air and moisture sensitive 1g 5g mc 7007 pentamethylcyclopentadienyllithium [51905-34-1 c h li fw 142.17 124.00125 10 15 85 280 air and moisture sensitive 1g 5g mc 2402 s biphenyl 3,4-dimethyl-1-cyclopentadienyl zirconiumiv r 1,1 binaphthyl-2 c h o zr fw 712.01 162.00125 46 36 2 85 280 100 mg 500 mg mc 2100 tetra-chloro-bistetrahydrofuranzirconium iv [21959-01-3 c h cl o zr fw 377.25 194.00125 8 16 4 2 290 900 moisture sensitive 10 g 50 g 50 210 page 32/35


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