GB1201515A - Method of preparing organotin compounds - Google Patents

Info

Publication number

GB1201515A

GB1201515A GB25604/68A GB2560468A GB1201515A GB 1201515 A GB1201515 A GB 1201515A GB 25604/68 A GB25604/68 A GB 25604/68A GB 2560468 A GB2560468 A GB 2560468A GB 1201515 A GB1201515 A GB 1201515A

Authority

GB

United Kingdom

Prior art keywords

dibenzyltin

radical

organotin compounds

dibutyltin

aromatic

Prior art date

1967-05-30

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired

Links

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• 150000001875 compounds Chemical class 0.000 title abstract 3
• -1 alkyl radical Chemical class 0.000 abstract 5
• 125000003118 aryl group Chemical group 0.000 abstract 3
• 150000003254 radicals Chemical class 0.000 abstract 2
• OBLHJVIUIHMHOM-UHFFFAOYSA-L C(C1=CC=CC=C1)(=O)[O-].C(C1=CC=CC=C1)(=O)[O-].C(C1=CC=CC=C1)[Sn+2]CC1=CC=CC=C1 Chemical compound C(C1=CC=CC=C1)(=O)[O-].C(C1=CC=CC=C1)(=O)[O-].C(C1=CC=CC=C1)[Sn+2]CC1=CC=CC=C1 OBLHJVIUIHMHOM-UHFFFAOYSA-L 0.000 abstract 1
• QMBQNHGAJUNECS-UHFFFAOYSA-L C(CCCCCCCCC(=O)[O-])(=O)[O-].C(C1=CC=CC=C1)[Sn+2]CC1=CC=CC=C1 Chemical compound C(CCCCCCCCC(=O)[O-])(=O)[O-].C(C1=CC=CC=C1)[Sn+2]CC1=CC=CC=C1 QMBQNHGAJUNECS-UHFFFAOYSA-L 0.000 abstract 1
• OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
• UFYYBMYIZKRDCG-UHFFFAOYSA-L [benzoyloxy(dioctyl)stannyl] benzoate Chemical compound [O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.CCCCCCCC[Sn+2]CCCCCCCC UFYYBMYIZKRDCG-UHFFFAOYSA-L 0.000 abstract 1
• LVIAVDPYLHRLNQ-UHFFFAOYSA-L [dibenzyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound C=1C=CC=CC=1C[Sn](OC(=O)CCCCCCCCCCC)(OC(=O)CCCCCCCCCCC)CC1=CC=CC=C1 LVIAVDPYLHRLNQ-UHFFFAOYSA-L 0.000 abstract 1
• UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 abstract 1
• NBJODVYWAQLZOC-UHFFFAOYSA-L [dibutyl(octanoyloxy)stannyl] octanoate Chemical compound CCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCC NBJODVYWAQLZOC-UHFFFAOYSA-L 0.000 abstract 1
• 125000001931 aliphatic group Chemical group 0.000 abstract 1
• 229910052783 alkali metal Inorganic materials 0.000 abstract 1
• 150000005840 aryl radicals Chemical class 0.000 abstract 1
• 125000004432 carbon atom Chemical group C* 0.000 abstract 1
• URUAAUSPFAHCOA-UHFFFAOYSA-L dibenzyltin(2+) hexanoate Chemical compound C(CCCCC)(=O)[O-].C(CCCCC)(=O)[O-].C(C1=CC=CC=C1)[Sn+2]CC1=CC=CC=C1 URUAAUSPFAHCOA-UHFFFAOYSA-L 0.000 abstract 1
• BNADHZBWFBSFQB-UHFFFAOYSA-L dibenzyltin(2+);hexanedioate Chemical compound [O-]C(=O)CCCCC([O-])=O.C=1C=CC=CC=1C[Sn+2]CC1=CC=CC=C1 BNADHZBWFBSFQB-UHFFFAOYSA-L 0.000 abstract 1
• NTEABVBMFIONGY-UHFFFAOYSA-L dibenzyltin(2+);octadecanoate Chemical compound C=1C=CC=CC=1C[Sn+2]CC1=CC=CC=C1.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O NTEABVBMFIONGY-UHFFFAOYSA-L 0.000 abstract 1
• 239000012975 dibutyltin dilaurate Substances 0.000 abstract 1
• SGIBEPSSERDAHS-UHFFFAOYSA-L dibutyltin(2+);hexanedioate Chemical compound CCCC[Sn+2]CCCC.[O-]C(=O)CCCCC([O-])=O SGIBEPSSERDAHS-UHFFFAOYSA-L 0.000 abstract 1
• 239000004094 surface-active agent Substances 0.000 abstract 1
• LNANSYMQXPWAEI-UHFFFAOYSA-M tribenzylstannyl acetate Chemical compound C=1C=CC=CC=1C[Sn](CC=1C=CC=CC=1)(OC(=O)C)CC1=CC=CC=C1 LNANSYMQXPWAEI-UHFFFAOYSA-M 0.000 abstract 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1