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1H-Indol-6-ol, 5-methoxy-, acetate (ester)

Base Information
  • Chemical Name:1H-Indol-6-ol, 5-methoxy-, acetate (ester)
  • CAS No.:112919-69-4
  • Molecular Formula:C11H11NO3
  • Molecular Weight:205.21000
  • Hs Code.:
1H-Indol-6-ol, 5-methoxy-, acetate (ester)

Synonyms:.acetic acid-(5-methoxy-indol-6-yl ester);.Essigsaeure-(5-methoxy-indol-6-ylester);.5-methoxy-6-acetoxyindole;.5-methoxy-6acetoxyindole;6-acetoxy-5-methoxyindole;

Suppliers and Price of 1H-Indol-6-ol, 5-methoxy-, acetate (ester)
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
  • 5-Acetoxy-6-methoxyindole
  • 200mg
  • $ 175.00
  • Biosynth Carbosynth
  • 5-Acetoxy-6-methoxyindole
  • 1 g
  • $ 150.00
  • Biosynth Carbosynth
  • 5-Acetoxy-6-methoxyindole
  • 500 mg
  • $ 90.00
  • Biosynth Carbosynth
  • 5-Acetoxy-6-methoxyindole
  • 250 mg
  • $ 50.00
  • Biosynth Carbosynth
  • 5-Acetoxy-6-methoxyindole
  • 2 g
  • $ 250.00
  • AccelPharmtech
  • 5-methoxy-1H-Indol-6-ol6-acetate 97.00%
  • 25G
  • $ 8510.00
  • AccelPharmtech
  • 5-methoxy-1H-Indol-6-ol6-acetate 97.00%
  • 5G
  • $ 4530.00
  • AccelPharmtech
  • 5-methoxy-1H-Indol-6-ol6-acetate 97.00%
  • 1G
  • $ 2640.00
Total 3 raw suppliers
Chemical Property of 1H-Indol-6-ol, 5-methoxy-, acetate (ester)
Chemical Property:
  • PSA:51.32000 
  • LogP:2.10180 
Purity/Quality:

95% *data from raw suppliers

5-Acetoxy-6-methoxyindole *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1H-Indol-6-ol, 5-methoxy-, acetate (ester)

There total 9 articles about 1H-Indol-6-ol, 5-methoxy-, acetate (ester) 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 4 steps
1: 98 percent / 4-(dimethylamino)pyridine / 1 h
2: KF, 18-crown-8 / propan-2-ol / 5 h
3: acetic anhydride, sodium acetate / overnight
4: 1.) H2; 2.) acetic anhydride, 4-(dimethylamino)pyridine / 1.) 5percent Pt/C / 1.) acetic acid, 15 psi, overnight; 2.) room temperature
With dmap; potassium fluoride; 18-crown-8; hydrogen; sodium acetate; acetic anhydride; platinum on activated charcoal; In isopropyl alcohol;
Guidance literature:
Multi-step reaction with 5 steps
1: CF3COOH / 60 °C
2: 98 percent / 4-(dimethylamino)pyridine / 1 h
3: KF, 18-crown-8 / propan-2-ol / 5 h
4: acetic anhydride, sodium acetate / overnight
5: 1.) H2; 2.) acetic anhydride, 4-(dimethylamino)pyridine / 1.) 5percent Pt/C / 1.) acetic acid, 15 psi, overnight; 2.) room temperature
With dmap; potassium fluoride; 18-crown-8; hydrogen; sodium acetate; acetic anhydride; trifluoroacetic acid; platinum on activated charcoal; In isopropyl alcohol;
Guidance literature:
Multi-step reaction with 3 steps
1: KF, 18-crown-8 / propan-2-ol / 5 h
2: acetic anhydride, sodium acetate / overnight
3: 1.) H2; 2.) acetic anhydride, 4-(dimethylamino)pyridine / 1.) 5percent Pt/C / 1.) acetic acid, 15 psi, overnight; 2.) room temperature
With dmap; potassium fluoride; 18-crown-8; hydrogen; sodium acetate; acetic anhydride; platinum on activated charcoal; In isopropyl alcohol;
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