SU170978A1 - - Google Patents

Info

Publication number

SU170978A1

SU170978A1 SU897419A SU897419A SU170978A1 SU 170978 A1 SU170978 A1 SU 170978A1 SU 897419 A SU897419 A SU 897419A SU 897419 A SU897419 A SU 897419A SU 170978 A1 SU170978 A1 SU 170978A1

Authority

SU

USSR - Soviet Union

Prior art keywords

complex

diaryl

dialkyl

calculated

product

Prior art date

Links

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• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
• 238000000034 method Methods 0.000 description 5
• 230000015572 biosynthetic process Effects 0.000 description 4
• 235000019441 ethanol Nutrition 0.000 description 4
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
• RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
• UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
• 238000004821 distillation Methods 0.000 description 3
• 229910000037 hydrogen sulfide Inorganic materials 0.000 description 3
• 238000003786 synthesis reaction Methods 0.000 description 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
• INJBDKCHQWVDGT-UHFFFAOYSA-N chloro(diethyl)phosphane Chemical compound CCP(Cl)CC INJBDKCHQWVDGT-UHFFFAOYSA-N 0.000 description 2
• USJRLGNYCQWLPF-UHFFFAOYSA-N chlorophosphane Chemical class ClP USJRLGNYCQWLPF-UHFFFAOYSA-N 0.000 description 2
• 238000000354 decomposition reaction Methods 0.000 description 2
• YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 2
• 238000003756 stirring Methods 0.000 description 2
• 229910000831 Steel Inorganic materials 0.000 description 1
• -1 alkyl alkyl ethyl phosphines Chemical class 0.000 description 1
• 235000010290 biphenyl Nutrition 0.000 description 1
• 239000004305 biphenyl Substances 0.000 description 1
• 125000006267 biphenyl group Chemical group 0.000 description 1
• 238000006243 chemical reaction Methods 0.000 description 1
• XGRJZXREYAXTGV-UHFFFAOYSA-N chlorodiphenylphosphine Chemical compound C=1C=CC=CC=1P(Cl)C1=CC=CC=C1 XGRJZXREYAXTGV-UHFFFAOYSA-N 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 239000012530 fluid Substances 0.000 description 1
• 238000004508 fractional distillation Methods 0.000 description 1
• 239000002917 insecticide Substances 0.000 description 1
• 230000003993 interaction Effects 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 239000000203 mixture Substances 0.000 description 1
• 239000012299 nitrogen atmosphere Substances 0.000 description 1
• ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 239000010959 steel Substances 0.000 description 1
• 230000009885 systemic effect Effects 0.000 description 1