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2-amino-5-iodoisophthalic acid

Base Information
  • Chemical Name:2-amino-5-iodoisophthalic acid
  • CAS No.:907574-30-5
  • Molecular Formula:C8H6INO4
  • Molecular Weight:307.044
  • Hs Code.:
2-amino-5-iodoisophthalic acid

Synonyms:2-amino-5-iodoisophthalic acid

Suppliers and Price of 2-amino-5-iodoisophthalic acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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  • Matrix Scientific
  • 2-Amino-5-iodoisophthalic acid 95%
  • 5g
  • $ 1666.00
  • Matrix Scientific
  • 2-Amino-5-iodoisophthalic acid 95%
  • 1g
  • $ 1110.00
Total 0 raw suppliers
Chemical Property of 2-amino-5-iodoisophthalic acid
Chemical Property:
Purity/Quality:

2-Amino-5-iodoisophthalic acid 95% *data from reagent suppliers

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Technology Process of 2-amino-5-iodoisophthalic acid

There total 1 articles about 2-amino-5-iodoisophthalic 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:
Guidance literature:
With Iodine monochloride; In acetic acid; at 20 ℃; for 2.25h;
Guidance literature:
2-amino-5-iodoisophthalic acid; orthoformic acid triethyl ester; With acetic acid; In toluene; at 100 ℃; for 25h;
3-amino-4-methyl benzoic acid methyl ester; In toluene; at 100 ℃; for 21h;
Guidance literature:
Multi-step reaction with 7 steps
1.1: 0.25 h / 170 - 185 °C
2.1: sulfuric acid / 32 h / Reflux
3.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 0.5 h
3.2: 48 h / 20 °C
4.1: triethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 16 h / 20 °C / Inert atmosphere
5.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 4 h / 65 °C
5.2: pH 5 / Acidic conditions
6.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 16 h / 20 °C
7.1: trifluoroacetic acid / 1 h / 85 °C
With lithium hydroxide monohydrate; sulfuric acid; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; N,N-dimethyl-formamide; acetonitrile;
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