2-(2-oxo-2,3-dihydro-1H-indol-6-yl)acetic acid

Base Information

Chemical Name:2-(2-oxo-2,3-dihydro-1H-indol-6-yl)acetic acid
CAS No.:101566-05-6
Molecular Formula:C₁₀H₉NO₃
Molecular Weight:191.186
Hs Code.:
European Community (EC) Number:843-338-1

Synonyms:101566-05-6;2-(2-oxo-2,3-dihydro-1H-indol-6-yl)acetic acid;2-(2-oxo-1,3-dihydroindol-6-yl)acetic Acid;2,3-dihydro-2-oxo-1H-Indole-6-acetic acid;2-(2-oxoindolin-6-yl)acetic acid;SCHEMBL5363902;SLTMYJVEPKGZTR-UHFFFAOYSA-N;BEA56605;AKOS004905491;CS-0233434;FT-0714266;EN300-133489;2-(2-oxo-2,3-dihydro-1H-indol-6-yl)aceticacid;Z1255415994

Suppliers and Price of 2-(2-oxo-2,3-dihydro-1H-indol-6-yl)acetic acid

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
2-(2-Oxo-2,3-dihydro-1H-indol-6-yl)aceticAcid
50mg
$ 285.00

TRC
2-(2-Oxo-2,3-dihydro-1H-indol-6-yl)aceticAcid
10mg
$ 65.00

AK Scientific
2-(2-Oxo-2,3-dihydro-1H-indol-6-yl)aceticacid
5g
$ 2894.00

AccelPharmtech
2,3-dihydro-2-oxo-1H-Indole-6-aceticacid 97.00%
25G
$ 13300.00

AccelPharmtech
2,3-dihydro-2-oxo-1H-Indole-6-aceticacid 97.00%
5G
$ 5360.00

AccelPharmtech
2,3-dihydro-2-oxo-1H-Indole-6-aceticacid 97.00%
1G
$ 3120.00

Total 3 raw suppliers

Chemical Property of 2-(2-oxo-2,3-dihydro-1H-indol-6-yl)acetic acid

Chemical Property:

XLogP3:0.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:191.058243149
Heavy Atom Count:14
Complexity:264

Purity/Quality:

98%min ^*data from raw suppliers

2-(2-Oxo-2,3-dihydro-1H-indol-6-yl)aceticAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C2=C(C=C(C=C2)CC(=O)O)NC1=O

Technology Process of 2-(2-oxo-2,3-dihydro-1H-indol-6-yl)acetic acid

There total 10 articles about 2-(2-oxo-2,3-dihydro-1H-indol-6-yl)acetic acid 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:

Reference yield:

: 1131604-64-2
methyl 2-(2-oxoindolin-6-yl)acetate

: 101566-05-6
indolone-6-acetic acid

Guidance literature:: With hydrogenchloride; In water; at 90 ℃; for 2h;

Reference yield:

: 192508-36-4
2-(4-fluoro-3-nitrophenyl)acetic acid

: 101566-05-6
indolone-6-acetic acid

Guidance literature:: Multi-step reaction with 6 steps

1: thionyl chloride / ethanol / 0 - 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

3: hydrogenchloride / water / 120 °C

4: thionyl chloride / 8 h / 0 - 20 °C

5: acetic acid; palladium on activated charcoal; hydrogen / 20 °C

6: hydrogenchloride / water / 2 h / 90 °C

With hydrogenchloride; thionyl chloride; palladium on activated charcoal; hydrogen; potassium carbonate; acetic acid; In ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 858972-16-4
ethyl 2-(4-fluoro-3-nitrophenyl)acetate

: 101566-05-6
indolone-6-acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

2: hydrogenchloride / water / 120 °C

3: thionyl chloride / 8 h / 0 - 20 °C

4: acetic acid; palladium on activated charcoal; hydrogen / 20 °C

5: hydrogenchloride / water / 2 h / 90 °C

With hydrogenchloride; thionyl chloride; palladium on activated charcoal; hydrogen; potassium carbonate; acetic acid; In water; N,N-dimethyl-formamide;