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4,7-DiMethoxy-6-azaindole Hydrochloride

Base Information
  • Chemical Name:4,7-DiMethoxy-6-azaindole Hydrochloride
  • CAS No.:917918-79-7
  • Molecular Formula:C9H10N2O2.ClH
  • Molecular Weight:214.652
  • Hs Code.:
  • Mol file:917918-79-7.mol
4,7-DiMethoxy-6-azaindole Hydrochloride

Synonyms:4,7-DIMETHOXY-1H-PYRROLO[2,3-C]PYRIDINE MONOHYDROCHLORIDE;4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridine hydrochloride;

Suppliers and Price of 4,7-DiMethoxy-6-azaindole Hydrochloride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 4,7-Dimethoxy-6-azaindoleHydrochloride
  • 1g
  • $ 1320.00
  • Crysdot
  • 4,7-Dimethoxy-1H-pyrrolo[2,3-c]pyridinehydrochloride 95+%
  • 1g
  • $ 888.00
  • Crysdot
  • 4,7-Dimethoxy-1H-pyrrolo[2,3-c]pyridinehydrochloride 95+%
  • 250mg
  • $ 355.00
  • Chemenu
  • 4,7-Dimethoxy-1H-pyrrolo[2,3-c]pyridinehydrochloride 95%+
  • 250mg
  • $ 731.00
  • Chemenu
  • 4,7-Dimethoxy-1H-pyrrolo[2,3-c]pyridinehydrochloride 95%+
  • 100mg
  • $ 548.00
  • Chemenu
  • 4,7-Dimethoxy-1H-pyrrolo[2,3-c]pyridinehydrochloride 95%+
  • 1g
  • $ 1462.00
  • Biosynth Carbosynth
  • 4,7-Dimethoxy-6-azaindole hydrochloride
  • 1 g
  • $ 1528.80
  • Biosynth Carbosynth
  • 4,7-Dimethoxy-6-azaindole hydrochloride
  • 500 mg
  • $ 840.00
  • Biosynth Carbosynth
  • 4,7-Dimethoxy-6-azaindole hydrochloride
  • 100 mg
  • $ 255.00
  • Biosynth Carbosynth
  • 4,7-Dimethoxy-6-azaindole hydrochloride
  • 50 mg
  • $ 140.00
Total 13 raw suppliers
Chemical Property of 4,7-DiMethoxy-6-azaindole Hydrochloride
Chemical Property:
  • PSA:47.14000 
  • LogP:2.38210 
  • Solubility.:Dimethyl Sulfoxide, Methanol, Water 
Purity/Quality:

97% *data from raw suppliers

4,7-Dimethoxy-6-azaindoleHydrochloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 4,7-Dimethoxy-6-azaindole Hydrochloride (cas# 917918-79-7) is a compound useful in organic synthesis.
Technology Process of 4,7-DiMethoxy-6-azaindole Hydrochloride

There total 2 articles about 4,7-DiMethoxy-6-azaindole Hydrochloride 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 5 steps
1.1: sulfuric acid; nitric acid / water / 7 h / 25 - 33 °C / Large scale
2.1: tert.-butylnitrite; sulfuric acid / 9.5 h / 20 - 43 °C / Large scale
3.1: N,N-dimethyl-formamide / 80 - 100 °C / Large scale
4.1: methanol; propanoic acid methyl ester; copper(l) iodide / tetrahydrofuran / 21 h / 30 - 72 °C / Large scale
5.1: 5%-palladium/activated carbon; hydrogen / ethyl acetate / 24 h / 25 - 35 °C / 1275.13 - 1500.15 Torr / Autoclave; Large scale
5.2: 10 - 30 °C / Large scale
With methanol; copper(l) iodide; tert.-butylnitrite; propanoic acid methyl ester; sulfuric acid; 5%-palladium/activated carbon; hydrogen; nitric acid; In tetrahydrofuran; water; ethyl acetate; N,N-dimethyl-formamide; 2.1: |Sandmeyer Reaction / 3.1: |Leimgruber-Batcho Indole Synthesis / 5.1: |Leimgruber-Batcho Indole Synthesis;
DOI:10.1021/acs.oprd.7b00134
Guidance literature:
Multi-step reaction with 5 steps
1.1: sulfuric acid; nitric acid / water / 7 h / 25 - 33 °C / Large scale
2.1: tert.-butylnitrite; sulfuric acid / 9.5 h / 20 - 43 °C / Large scale
3.1: N,N-dimethyl-formamide / 80 - 100 °C / Large scale
4.1: methanol; propanoic acid methyl ester; copper(l) iodide / tetrahydrofuran / 21 h / 30 - 72 °C / Large scale
5.1: formic acid; triethylamine; palladium 10% on activated carbon / tetrahydrofuran; ethanol / 7 h / 50 - 55 °C / Large scale
5.2: Large scale
With methanol; copper(l) iodide; formic acid; tert.-butylnitrite; propanoic acid methyl ester; sulfuric acid; palladium 10% on activated carbon; nitric acid; triethylamine; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; 2.1: |Sandmeyer Reaction / 3.1: |Leimgruber-Batcho Indole Synthesis;
DOI:10.1021/acs.oprd.7b00134
Guidance literature:
Multi-step reaction with 7 steps
1.1: trichlorophosphate / neat (no solvent) / 15 h / 40 - 102 °C / Large scale
2.1: methanol / toluene / 8 h / 45 - 55 °C / Large scale
3.1: Methyl isobutyl carbinol / 76 h / 130 - 145 °C / Large scale
4.1: isopropylmagnesium chloride; pyridine / 2-methyltetrahydrofuran / -25 - -10 °C / Large scale
4.2: 3 h / -25 - -10 °C / Large scale
5.1: tetra-(n-butyl)ammonium iodide; potassium carbonate / acetonitrile / 16 h / 20 °C / Large scale
6.1: potassium carbonate / acetonitrile / 4 h / 20 - 25 °C / Large scale
6.2: 12 h / 85 °C / Large scale
7.1: chlorine; water / dichloromethane / 0 °C
With pyridine; methanol; Methyl isobutyl carbinol; water; isopropylmagnesium chloride; chlorine; tetra-(n-butyl)ammonium iodide; potassium carbonate; trichlorophosphate; In 2-methyltetrahydrofuran; dichloromethane; toluene; acetonitrile;
DOI:10.1021/acs.oprd.7b00134
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