SU282313A1 - - Google Patents

Info

Publication number

SU282313A1

SU282313A1 SU1151321A SU1151321A SU282313A1 SU 282313 A1 SU282313 A1 SU 282313A1 SU 1151321 A SU1151321 A SU 1151321A SU 1151321 A SU1151321 A SU 1151321A SU 282313 A1 SU282313 A1 SU 282313A1

Authority

SU

USSR - Soviet Union

Prior art keywords

hydrazide

water

hydrazine hydrate

phenolcarboxylic

mol

Prior art date

Links

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• 238000000034 method Methods 0.000 description 7
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
• NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 5
• 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 5
• IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 5
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
• CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
• 230000015572 biosynthetic process Effects 0.000 description 3
• 238000003786 synthesis reaction Methods 0.000 description 3
• 239000008096 xylene Substances 0.000 description 3
• KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 2
• XSXYESVZDBAKKT-UHFFFAOYSA-N 2-hydroxybenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1O XSXYESVZDBAKKT-UHFFFAOYSA-N 0.000 description 2
• 238000010533 azeotropic distillation Methods 0.000 description 2
• 238000009835 boiling Methods 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• 150000002148 esters Chemical class 0.000 description 2
• OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• 239000003960 organic solvent Substances 0.000 description 2
• 150000007965 phenolic acids Chemical class 0.000 description 2
• 239000011541 reaction mixture Substances 0.000 description 2
• YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
• 239000002250 absorbent Substances 0.000 description 1
• 230000002745 absorbent Effects 0.000 description 1
• 239000002253 acid Substances 0.000 description 1
• 239000007844 bleaching agent Substances 0.000 description 1
• 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
• 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
• 239000013078 crystal Substances 0.000 description 1
• 230000003993 interaction Effects 0.000 description 1
• 239000000543 intermediate Substances 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• QSGONIQEKLJPGV-UHFFFAOYSA-N methyl 3,5-ditert-butyl-2-hydroxybenzoate Chemical compound COC(=O)C1=CC(C(C)(C)C)=CC(C(C)(C)C)=C1O QSGONIQEKLJPGV-UHFFFAOYSA-N 0.000 description 1
• 229960001047 methyl salicylate Drugs 0.000 description 1
• 238000009994 optical bleaching Methods 0.000 description 1
• 239000004476 plant protection product Substances 0.000 description 1
• 229920000642 polymer Polymers 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 239000003381 stabilizer Substances 0.000 description 1
• 239000012209 synthetic fiber Substances 0.000 description 1
• 229920002994 synthetic fiber Polymers 0.000 description 1

Cited By (1)