O₂CC₆H₄NH₂-o^(1-)

Base Information

• Chemical Name: O₂CC₆H₄NH₂-o^(1-)
• CAS No.: 1462-61-9
• Molecular Formula: C₇H₆NO₂
• Molecular Weight: 136.13
• Mol file: 1462-61-9.mol

Synonyms:O₂CC₆H₄NH₂-o^(1-)

Chemical Property of O₂CC₆H₄NH₂-o^(1-)

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of O₂CC₆H₄NH₂-o^(1-)

There total 4 articles about O₂CC₆H₄NH₂-o^(1-) 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:

methyl red (493-52-7) → O2CC6H4NH2-o(1-) (1462-61-9) + 4-amino-N,N-dimethylaniline (99-98-9)

Guidance literature:

With sodium tetrahydroborate; water; at 21 - 23 ℃; Reagent/catalyst; Kinetics; Catalytic behavior;

DOI:10.1002/cctc.201900260

Reference yield:

(-)-chorismate (159700-65-9) → salicylate (63-36-5,38504-14-2,45749-46-0) + O2CC6H4NH2-o(1-) (1462-61-9)

Guidance literature:

With L-glutamine; DL-dithiothreitol; Salmonella typhimurium TrpE; Salmonella typhimurium TrpG; magnesium chloride; In aq. phosphate buffer; at 25 ℃; for 3h; pH=7; Reagent/catalyst; Enzymatic reaction;

DOI:10.1002/anie.201505063

Reference yield:

(-)-chorismate (159700-65-9) → salicylate (63-36-5,38504-14-2,45749-46-0) + O2CC6H4NH2-o(1-) (1462-61-9) + isochorismate

Guidance literature:

With L-glutamine; anthranilate synthase Q₁₄₇K mutant; magnesium chloride; at 25 ℃; for 3h; pH=7; aq. phosphate buffer; Enzymatic reaction;

DOI:10.1021/bi100021x

upstream raw materials:

(-)-chorismate

methyl red

Downstream raw materials:

Co(II) o-aminobenzoate