6-Methoxy-2-phenylpyrimidine-4-carboxylic acid

Base Information

• Chemical Name: 6-Methoxy-2-phenylpyrimidine-4-carboxylic acid
• CAS No.: 85815-04-9
• Molecular Formula: C₁₂H₁₀N₂O₃
• Molecular Weight: 230.223
• Hs Code.: 2933599090
• DSSTox Substance ID: DTXSID30511356
• Wikidata: Q82370108
• Mol file: 85815-04-9.mol

Synonyms:6-methoxy-2-phenylpyrimidine-4-carboxylic acid;85815-04-9;SCHEMBL2580556;DTXSID30511356;MFCD16710279;AKOS005766002;GE-0701;SB59201;FT-0682000;6-methoxy-2-phenylpyrimidine-4-carboxylicacid;J-518844

Chemical Property of 6-Methoxy-2-phenylpyrimidine-4-carboxylic acid

Chemical Property:

• PSA: 72.31000
• LogP: 1.85040
• XLogP3: 2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 230.06914219
• Heavy Atom Count: 17
• Complexity: 267

Purity/Quality:

98%min ^*data from raw suppliers

6-Methoxy-2-phenylpyrimidine-4-carboxylic acid >95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=NC(=NC(=C1)C(=O)O)C2=CC=CC=C2

Technology Process of 6-Methoxy-2-phenylpyrimidine-4-carboxylic acid

There total 2 articles about 6-Methoxy-2-phenylpyrimidine-4-carboxylic 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:

4-chloro-6-methyl-2-phenyl-pyrimidine (29509-92-0) → 4-methoxy-2-phenylpyrimidine-6-carboxylic acid (85815-04-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 95.7 percent / methanol / 5 h / Heating

2: 26.7 percent / SeO₂ / pyridine / 50 h / Heating

With selenium(IV) oxide; In pyridine; methanol;

DOI:10.1248/cpb.30.4314

Reference yield:

6-methyl-2-phenylpyrimidin-4-ol (13514-79-9) → 4-methoxy-2-phenylpyrimidine-6-carboxylic acid (85815-04-9)

Guidance literature:

Multi-step reaction with 3 steps

1: 97 percent / POCl₃ / 3.5 h / Heating

2: 95.7 percent / methanol / 5 h / Heating

3: 26.7 percent / SeO₂ / pyridine / 50 h / Heating

With selenium(IV) oxide; trichlorophosphate; In pyridine; methanol;

DOI:10.1248/cpb.30.4314

Reference yield:

4-methoxy-2-phenylpyrimidine-6-carboxylic acid (85815-04-9) → 6-cyano-2-methoxy-4-phenylpyrimidine (85830-27-9)

Guidance literature:

Multi-step reaction with 3 steps

1: SOCl₂ / 2 h / Heating

2: 1.18 g / aq. NH₄OH / benzene / 2.5 h / Ambient temperature

3: 96 percent / POCl₃ / 1 h / Heating

With ammonium hydroxide; thionyl chloride; trichlorophosphate; In benzene;

DOI:10.1248/cpb.30.4314

upstream raw materials:

4-chloro-6-methyl-2-phenyl-pyrimidine

6-methyl-2-phenylpyrimidin-4-ol

Downstream raw materials:

6-cyano-2-methoxy-4-phenylpyrimidine

6-Methoxy-2-phenyl-pyrimidine-4-carboxylic acid amide

2-Phenyl-6-(1H-tetrazol-5-yl)-pyrimidin-4-ol

4-Methoxy-2-phenyl-6-(1H-tetrazol-5-yl)-pyrimidine

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