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5-dimethylamino-1-formylisoquinoline-2-oxide p-toluenesulfonyl hydrazone

Base Information
  • Chemical Name:5-dimethylamino-1-formylisoquinoline-2-oxide p-toluenesulfonyl hydrazone
  • CAS No.:75795-51-6
  • Molecular Formula:C19H20N4O3S
  • Molecular Weight:384.459
  • Hs Code.:
5-dimethylamino-1-formylisoquinoline-2-oxide p-toluenesulfonyl hydrazone

Synonyms:

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Chemical Property of 5-dimethylamino-1-formylisoquinoline-2-oxide p-toluenesulfonyl hydrazone
Chemical Property:
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Technology Process of 5-dimethylamino-1-formylisoquinoline-2-oxide p-toluenesulfonyl hydrazone

There total 10 articles about 5-dimethylamino-1-formylisoquinoline-2-oxide p-toluenesulfonyl hydrazone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 12 steps
1: 93 percent / conc. hydrochlorid acid / 5 h / 100 °C
2: 94 percent / conc. sulfuric acid / 3 h / Heating
3: H2 / 5 percent palladium on charcoal / ethanol / Ambient temperature
4: acetic anhydride / Ambient temperature
5: 1.) sodium hydride / 1.) THF, reflux, 30 min., 2.) THF, reflux, 3 h
6: 1.) LiALH4, conc. sulfuric acid, 2.) chloranil / 1.) THF, 0 deg C , 1 h; THF, reflux, 2 h, 2.) ethylacetate, 10 min., RT
7: Ambient temperature
8: 47 percent / m-chloroperbenzoic acid / methanol / 5 h / Ambient temperature
9: 70 percent / carbon disulfide / methanol / 1 h / Heating
10: 88 percent / conc. ammonia / ethanol / 1 h
11: selenium dioxide / pyridine / 5 h / Heating
12: benzene / 1 h / Ambient temperature
With hydrogenchloride; carbon disulfide; ammonium hydroxide; lithium aluminium tetrahydride; selenium(IV) oxide; sulfuric acid; hydrogen; acetic anhydride; chloranil; sodium hydride; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In pyridine; methanol; ethanol; benzene;
Guidance literature:
Multi-step reaction with 10 steps
1: H2 / 5 percent palladium on charcoal / ethanol / Ambient temperature
2: acetic anhydride / Ambient temperature
3: 1.) sodium hydride / 1.) THF, reflux, 30 min., 2.) THF, reflux, 3 h
4: 1.) LiALH4, conc. sulfuric acid, 2.) chloranil / 1.) THF, 0 deg C , 1 h; THF, reflux, 2 h, 2.) ethylacetate, 10 min., RT
5: Ambient temperature
6: 47 percent / m-chloroperbenzoic acid / methanol / 5 h / Ambient temperature
7: 70 percent / carbon disulfide / methanol / 1 h / Heating
8: 88 percent / conc. ammonia / ethanol / 1 h
9: selenium dioxide / pyridine / 5 h / Heating
10: benzene / 1 h / Ambient temperature
With carbon disulfide; ammonium hydroxide; lithium aluminium tetrahydride; selenium(IV) oxide; sulfuric acid; hydrogen; acetic anhydride; chloranil; sodium hydride; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In pyridine; methanol; ethanol; benzene;
Guidance literature:
Multi-step reaction with 9 steps
1: acetic anhydride / Ambient temperature
2: 1.) sodium hydride / 1.) THF, reflux, 30 min., 2.) THF, reflux, 3 h
3: 1.) LiALH4, conc. sulfuric acid, 2.) chloranil / 1.) THF, 0 deg C , 1 h; THF, reflux, 2 h, 2.) ethylacetate, 10 min., RT
4: Ambient temperature
5: 47 percent / m-chloroperbenzoic acid / methanol / 5 h / Ambient temperature
6: 70 percent / carbon disulfide / methanol / 1 h / Heating
7: 88 percent / conc. ammonia / ethanol / 1 h
8: selenium dioxide / pyridine / 5 h / Heating
9: benzene / 1 h / Ambient temperature
With carbon disulfide; ammonium hydroxide; lithium aluminium tetrahydride; selenium(IV) oxide; sulfuric acid; acetic anhydride; chloranil; sodium hydride; 3-chloro-benzenecarboperoxoic acid; In pyridine; methanol; ethanol; benzene;
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