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[ CAS No. 4741-58-6 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 4741-58-6
Chemical Structure| 4741-58-6
Chemical Structure| 4741-58-6
Structure of 4741-58-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 4741-58-6 ]

CAS No. :4741-58-6 MDL No. :MFCD00126369
Formula : C10H10O4 Boiling Point : -
Linear Structure Formula :- InChI Key :ZXIMTZPOPPEWHU-UHFFFAOYSA-N
M.W :194.18 Pubchem ID :12637623
Synonyms :

Safety of [ 4741-58-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 4741-58-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 4741-58-6 ]

[ 4741-58-6 ] Synthesis Path-Downstream   1~31

  • 1
  • [ 4741-58-6 ]
  • 4,5-dimethoxy-7-nitro-phthalide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With nitric acid
  • 2
  • [ 1567-56-2 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
With acetic acid; zinc
  • 3
  • [ 50-00-0 ]
  • [ 1522-67-4 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
Multistep reaction;
  • 4
  • [ 4741-58-6 ]
  • [ 123-72-8 ]
  • [ 116541-29-8 ]
YieldReaction ConditionsOperation in experiment
Yield given. Multistep reaction;
  • 5
  • [ 4741-58-6 ]
  • [ 95-92-1 ]
  • [ 106076-05-5 ]
YieldReaction ConditionsOperation in experiment
20% With sodium ethanolate In diethyl ether for 10h; Ambient temperature;
  • 6
  • [ 4741-58-6 ]
  • [ 98664-75-6 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide
  • 7
  • [ 201230-82-2 ]
  • [ 5653-67-8 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
With magnesium oxide; trifluoroacetic acid; lithium chloride; palladium dichloride; thallium(III) trifluoroacetate 1.) THF, 25 deg C, 18 h, 2.) MeOH, room temperature, overnight; Yield given. Multistep reaction;
  • 8
  • [ 201230-82-2 ]
  • [ 74785-03-8 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
78% With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 60h;
77% With sodium methylate In methanol at 25℃;
  • 9
  • 2-Hydroxymethyl-3,4-dimethoxy-benzonitrile [ No CAS ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide In methanol; water Heating; Yield given;
  • 10
  • [ 50-00-0 ]
  • [ 57193-17-6 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
With n-butyllithium 1.) n-hexane, THF, -45 deg C, 2 h, 2.) a) n-hexane, THF, -45 deg C, 1 h, b) RT, overnight; Yield given. Multistep reaction;
YieldReaction ConditionsOperation in experiment
Narkotinogendiol-metho-hydroxid, aq. KOH, Δ (neben 6-Methoxy-4,5-methylendioxy-2-vinyl-1-dimethylamino-benzol);
aus Isobenzofuranon 16, CH2N2;
Hydrastindiol-methjodid, sd. NaOH (neben N,N-Dimethyl-2-methoxy-3,4-methylendioxy-6-vinyl-benzylamin od. der methoxylfreien Verb.);
Narcotindiol-methjodid, sd. NaOH (neben N,N-Dimethyl-2-methoxy-3,4-methylendioxy-6-vinyl-benzylamin od. der methoxylfreien Verb.);
monomeres u. polymeres 2-Hydroxymethyl-3,4-dimethoxy-benzaldehyd, 40percent-ig. KOH, Δ, Dampfbad;
aus (+-)-Alpinigenin-diol (XXI), MnO2;

YieldReaction ConditionsOperation in experiment
With sodium hydroxide
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; tin Behandeln der filtrierten Loesung mit Natriumnitrit und Ansaeuern mit Salzsaeure;
YieldReaction ConditionsOperation in experiment
With sodium amalgam; sodium carbonate
  • 15
  • [ 4741-58-6 ]
  • [ 518-90-1 ]
YieldReaction ConditionsOperation in experiment
at 20℃;
  • 16
  • [ 4741-58-6 ]
  • 2-hydroxymethyl-3,4-dimethoxy-benzoic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
Versetzen mit Saeure;
  • 18
  • [ 4741-58-6 ]
  • [ 7697-37-2 ]
  • [ 6279-83-0 ]
YieldReaction ConditionsOperation in experiment
at 150 - 155℃;
  • 19
  • [ 518-90-1 ]
  • [ 7732-18-5 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
Electrolysis;
  • 20
  • [ 123796-70-3 ]
  • [ 7732-18-5 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
Electrolysis;
  • 21
  • [ 5653-67-8 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 67 percent / iodine, silver trifluoroacetate / CHCl3 2: 78 percent / potassium carbonate / PdCl2(PPh3)2 / dimethylformamide / 60 h / 50 °C / 3040 Torr
  • 22
  • [ 74785-03-8 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: dimethylformamide / 0.5 h / 110 °C 2: potassium hydroxyde / H2O; methanol / Heating
  • 23
  • [ 4741-58-6 ]
  • [ 91652-79-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 2: 99 percent / pyridine / benzene / 1 h / Heating 3: 74 percent / 1,8-diazabicylo<5.4.0>undec-7-ene (DBU) / benzene / 1 h / Heating 4: 81 percent / BBr3 / CH2Cl2 / 1.) 0 deg C, 30 min, 2.) RT, 3 h
  • 24
  • [ 4741-58-6 ]
  • [ 116541-08-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 2: 99 percent / pyridine / benzene / 1 h / Heating 3: 4 percent / 1,8-diazabicylo<5.4.0>undec-7-ene (DBU) / benzene / 1 h / Heating
  • 25
  • [ 4741-58-6 ]
  • (Z)-3-butylidene-4,5-dimethoxyphthalide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 2: 99 percent / pyridine / benzene / 1 h / Heating 3: 74 percent / 1,8-diazabicylo<5.4.0>undec-7-ene (DBU) / benzene / 1 h / Heating
  • 26
  • [ 4741-58-6 ]
  • [ 116541-31-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 2: 99 percent / pyridine / benzene / 1 h / Heating
  • 27
  • [ 4741-58-6 ]
  • [ 98664-74-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: NBS 2: 55 percent / triethylamine / acetone / 96 h / Ambient temperature
  • 28
  • [ 4741-58-6 ]
  • [ 1012323-56-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: NBS 2: 55 percent / triethylamine / acetone / 96 h / Ambient temperature 3: trifluoroacetic acid / CH2Cl2 / Ambient temperature
  • 29
  • [ 4741-58-6 ]
  • 4,5-dimethoxy-3-(4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-<i>g</i>]isoquinolin-5-yl)-7-nitro-phthalide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: aqueous nitric acid 2: ethanol
  • 30
  • [ 623-27-8 ]
  • [ 110451-87-1 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
64% Stage #1: terephthalaldehyde, With palladium 10% on activated carbon; sodium carbonate In isopropyl alcohol at 120℃; for 24h; Inert atmosphere; Stage #2: 2-bromomethyl-1-iodo-4,5-dimethoxybenzene With triphenylphosphine In 1-methyl-pyrrolidin-2-one at 100℃; for 24h; Inert atmosphere;
  • 31
  • [ 50-00-0 ]
  • [ 22792-13-8 ]
  • [ 531-88-4 ]
  • [ 4741-58-6 ]
YieldReaction ConditionsOperation in experiment
1: 50% 2: 42% With silver hexafluoroantimonate; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 In dichloromethane at 160℃; for 72h; Inert atmosphere; Sealed tube; regioselective reaction;
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