3-Quinolinol, 8-methyl-

Base Information

Chemical Name:3-Quinolinol, 8-methyl-
CAS No.:25369-30-6
Molecular Formula:C10H9NO
Molecular Weight:
Hs Code.:
Mol file:25369-30-6.mol

Synonyms:

Suppliers and Price of 3-Quinolinol, 8-methyl-

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

Total 7 raw suppliers

Chemical Property of 3-Quinolinol, 8-methyl-

Chemical Property:

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 3-Quinolinol, 8-methyl-

There total 3 articles about 3-Quinolinol, 8-methyl- 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: 13.0%

: 611-32-5
8-methylquinoline

: 16032-35-2
8-hydroxymethylquinoline

: 16026-71-4
5-hydroxy-8-methylquinoline

: 25369-30-6
3-hydroxy-8-methylquinoline

: 7b-methyl-1a,7b-dihydrooxireno[2,3-h]quinoline

Guidance literature:: With glucose dehydrogenase; D-glucose; cytochrome P₄₅₀ enzyme CYP₁₀₂A₁ R₄₇L/Y₅₁F/H₁₇₁L/I₂₆₃A/Q₃₀₇H/N₃₁₉Y/A₃₂₈L mutant; C₂₁H₂₅N₇O₁₇P₃^(3-)*2H⁽¹⁺⁾*Na⁽¹⁺⁾; In aq. phosphate buffer; ethanol; at 20 ℃; for 12h; pH=8.4; Reagent/catalyst; Catalytic behavior; Enzymatic reaction;
DOI:10.1002/anie.201904157

Reference yield:

: 52601-70-4
8-methyl-1,2,3,4-tetrahydroquinoline

: 16032-35-2
8-hydroxymethylquinoline

: 16026-71-4
5-hydroxy-8-methylquinoline

: 25369-30-6
3-hydroxy-8-methylquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: cytochrome P₄₅₀ enzyme CYP₁₀₂A₁ R₄₇L/Y₅₁F/H₁₇₁L/I₂₆₃G/Q₃₀₇H/N₃₁₉Y/A₃₂₈L mutant; D-glucose; glucose dehydrogenase; C₂₁H₂₅N₇O₁₇P₃^(3-)*2H⁽¹⁺⁾*Na⁽¹⁺⁾ / ethanol; aq. phosphate buffer / 16 h / 20 °C / pH 8.4 / Enzymatic reaction

2: cytochrome P₄₅₀ enzyme CYP₁₀₂A₁ R₄₇L/Y₅₁F/H₁₇₁L/I₂₆₃A/Q₃₀₇H/N₃₁₉Y/A₃₂₈L mutant; D-glucose; glucose dehydrogenase; C₂₁H₂₅N₇O₁₇P₃^(3-)*2H⁽¹⁺⁾*Na⁽¹⁺⁾ / ethanol; aq. phosphate buffer / 12 h / 20 °C / pH 8.4 / Enzymatic reaction

With glucose dehydrogenase; D-glucose; cytochrome P₄₅₀ enzyme CYP₁₀₂A₁ R₄₇L/Y₅₁F/H₁₇₁L/I₂₆₃A/Q₃₀₇H/N₃₁₉Y/A₃₂₈L mutant; cytochrome P₄₅₀ enzyme CYP₁₀₂A₁ R₄₇L/Y₅₁F/H₁₇₁L/I₂₆₃G/Q₃₀₇H/N₃₁₉Y/A₃₂₈L mutant; C₂₁H₂₅N₇O₁₇P₃^(3-)*2H⁽¹⁺⁾*Na⁽¹⁺⁾; In aq. phosphate buffer; ethanol;
DOI:10.1002/anie.201904157