4-Bromo-1-methyl-3-propyl-1H-pyrazole-5-carboxylic acid

Base Information

• Chemical Name: 4-Bromo-1-methyl-3-propyl-1H-pyrazole-5-carboxylic acid
• CAS No.: 128537-50-8
• Molecular Formula: C₈H₁₁BrN₂O₂
• Molecular Weight: 247.092
• Hs Code.: 2933199090
• DSSTox Substance ID: DTXSID70467742
• Wikidata: Q82294803
• Mol file: 128537-50-8.mol

Synonyms:4-Bromo-1-methyl-3-propyl-1H-pyrazole-5-carboxylic acid;128537-50-8;4-BROMO-2-METHYL-5-PROPYLPYRAZOLE-3-CARBOXYLIC ACID;4-Bromo-1-methyl-3-propyl-1H-pyrazole-5-carboxylicacid;DTXSID70467742;AKOS015997374;VS-10190;CS-0329094;A805836

Chemical Property of 4-Bromo-1-methyl-3-propyl-1H-pyrazole-5-carboxylic acid

Chemical Property:

• PSA: 55.12000
• LogP: 1.83330
• XLogP3: 2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 246.00039
• Heavy Atom Count: 13
• Complexity: 201

Purity/Quality:

97% ^*data from raw suppliers

4-Bromo-1-methyl-3-propyl-1H-pyrazole-5-carboxylicacid 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCC1=NN(C(=C1Br)C(=O)O)C

Technology Process of 4-Bromo-1-methyl-3-propyl-1H-pyrazole-5-carboxylic acid

There total 1 articles about 4-Bromo-1-methyl-3-propyl-1H-pyrazole-5-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: 88.0%

1-methyl-3-propyl-1 H-pyrazole-5-carboxylic acid (139755-99-0) → 4-bromo-1-methyl-3-propyl-1H-pyrazole-5-carboxylic acid (128537-50-8)

Guidance literature:

With bromine; potassium carbonate; In dichloromethane; at 20 ℃; for 6h;

DOI:10.1002/jhet.5570420608

Reference yield:

4-bromo-1-methyl-3-propyl-1H-pyrazole-5-carboxylic acid (128537-50-8) → 5-(3-nitrophenyl)-1-methyl-3-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one

Guidance literature:

Multi-step reaction with 4 steps

1: thionyl chloride / 2 h / Heating

2: 0.21 g / aq. NH₄OH / 2 h / 20 °C

3: 17 percent / basic alumina / 0.1 h / microwave irradiation

4: 99 percent / basic alumina / 0.02 h / microwave irradiation

With aluminum oxide; ammonium hydroxide; thionyl chloride;

DOI:10.1002/jhet.5570420608

Reference yield:

4-bromo-1-methyl-3-propyl-1H-pyrazole-5-carboxylic acid (128537-50-8) → 5-(3-bromophenyl)-1-methyl-3-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one

Guidance literature:

Multi-step reaction with 3 steps

1: thionyl chloride / 2 h / Heating

2: 0.21 g / aq. NH₄OH / 2 h / 20 °C

3: 62 percent / basic alumina / 0.12 h / microwave irradiation

With aluminum oxide; ammonium hydroxide; thionyl chloride;

DOI:10.1002/jhet.5570420608

upstream raw materials:

1-methyl-3-propyl-1 H-pyrazole-5-carboxylic acid

Downstream raw materials:

4-[(3-bromobenzoyl)amino]-1-methyl-3-propyl-1H-pyrazole-5-carboxamide

4-[(3-nitrobenzoyl)amino]-1-methyl-3-propyl-1H-pyrazole-5-carboxamide

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