Pyrazoles

eMolecules​ 41330-49-8 | 3-CHLORO-1H-INDAZOL-5-AMINE | AstaTech | MFCD07781654 | 167.600 | C7H6ClN3 | 95.000 | Nc1ccc2[nH]nc(Cl)c2c1 | 1g | 290672581

3-CHLORO-1H-INDAZOL-5-AMINE | AstaTech | 41330-49-8 | MFCD07781654 | 167.600 | C7H6ClN3 | 95.000 | Nc1ccc2[nH]nc(Cl)c2c1 | 1g | 290672581

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eMolecules​ 35344-95-7 | 1H-Pyrazole-4-carboxaldehyde | Ambeed | MFCD02179514 | 96.089 | C4H4N2O | 97.000 | O=Cc1cn[nH]c1 | 250mg | 552730412

1H-Pyrazole-4-carboxaldehyde | Ambeed | 35344-95-7 | MFCD02179514 | 96.089 | C4H4N2O | 97.000 | O=Cc1cn[nH]c1 | 250mg | 552730412

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eMolecules​ 1316852-65-9 | 5-Bromo-2-methyl-2H-pyrazolo[3,4-b]pyridine | Combi-Blocks, Inc. | MFCD19443914 | 212.050 | C7H6BrN3 | 97.000 | Cn1cc2cc(Br)cnc2n1 | 25g | 837464092

5-Bromo-2-methyl-2H-pyrazolo[3,4-b]pyridine | Combi-Blocks, Inc. | 1316852-65-9 | MFCD19443914 | 212.050 | C7H6BrN3 | 97.000 | Cn1cc2cc(Br)cnc2n1 | 25g | 837464092

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eMolecules​ 35344-95-7 | 1H-pyrazole-4-carbaldehyde | Pharmablock | MFCD02179514 | 96.089 | C4H4N2O | 97.000 | O=Cc1cn[nH]c1 | 1g | 551086747

1H-pyrazole-4-carbaldehyde | Pharmablock | 35344-95-7 | MFCD02179514 | 96.089 | C4H4N2O | 97.000 | O=Cc1cn[nH]c1 | 1g | 551086747

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eMolecules​ 35344-95-7 | 1H-pyrazole-4-carbaldehyde | Pharmablock | MFCD02179514 | 96.089 | C4H4N2O | 97.000 | O=Cc1cn[nH]c1 | 5g | 551086748

1H-pyrazole-4-carbaldehyde | Pharmablock | 35344-95-7 | MFCD02179514 | 96.089 | C4H4N2O | 97.000 | O=Cc1cn[nH]c1 | 5g | 551086748

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eMolecules​ 35344-95-7 | 1H-Pyrazole-4-carboxaldehyde | Ambeed | MFCD02179514 | 96.089 | C4H4N2O | 97.000 | O=Cc1cn[nH]c1 | 5g | 490561626

1H-Pyrazole-4-carboxaldehyde | Ambeed | 35344-95-7 | MFCD02179514 | 96.089 | C4H4N2O | 97.000 | O=Cc1cn[nH]c1 | 5g | 490561626

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AA BLOCKS LLC 4-3 5-DIMETHYL-1H-PYRAZOL-1G

NC3371819 4-3 5-DIMETHYL-1H-PYRAZOL-1G

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ACCUSTANDARD INC 1H 1H 2H 2H-PERFLUOROOCTANE SU

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NC3369648 1H 1H 2H 2H-PERFLUOROOCTANE SU

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Medchemexpress LLC Pyrazole-3-carboxylic acid | 1621-91-6 | MFCD00077436 | 112.09 | 100 G

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Pyrazole-3-carboxylic acid is an alternative anchoring group to carboxylic acid in phthalocyanine dyes, exhibiting flexible coordination modes. It can chelate to metal ions to form stable complexes via its N and O atoms. This compound can be utilized in the synthesis of derivatives with various biological activities.

• Serves as an alternative anchoring group in phthalocyanine dyes
• Exhibits flexible coordination modes with metal ions
• Forms stable complexes with metal ions via N and O atoms
• Used in the synthesis of derivatives with antibacterial activity
• Used in the synthesis of derivatives with anti-inflammatory activity
• Used in the synthesis of derivatives with ulcerogenic liability
• Used in the synthesis of derivatives with antiproliferative activities

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Aobchem AOBCHEM

5000945743 1- 4-ISOPROPOXYPHENYL -2 2-DIM

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Aobchem AOBCHEM

5000940824 1- 4-METHYLPHENYL -1H-PYRAZOLE

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eMolecules​ 1020174-04-2 | 1-Methyl-1H-pyrazole-3-boronic acid pinacol ester | Combi-Blocks, Inc. | MFCD04114000 | 208.070 | C10H17BN2O2 | 97.000 | Cn1ccc(n1)B1OC(C)(C)C(C)(C)O1 | 25g | 569291035

1-Methyl-1H-pyrazole-3-boronic acid pinacol ester | Combi-Blocks, Inc. | 1020174-04-2 | MFCD04114000 | 208.070 | C10H17BN2O2 | 97.000 | Cn1ccc(n1)B1OC(C)(C)C(C)(C)O1 | 25g | 569291035

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Medchemexpress LLC Allopurinol (Standard) | 315-30-0 | 599413 | 99.97% | 25 MG

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Allopurinol (Standard) is the analytical standard of Allopurinol, intended for research and analytical applications. It is a potent and orally active xanthine oxidase inhibitor, utilized in the research of hyperuricemia and gout. It also decreases the expression of HIF-1α and HIF-2α proteins, and exhibits anti-depressant, anti-nociception, and anti-leishmanial activities.

• Potent and orally active xanthine oxidase inhibitor
• Used in research of hyperuricemia and gout
• Decreases expression of HIF-1α and HIF-2α protein
• Shows anti-depressant and anti-nociception activity
• Exhibits anti-leishmanial effect

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Aobchem AOBCHEM

5000950661 1- TERT-BUTYL -1H-PYRAZOLE-4-C

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Aobchem AOBCHEM

5000951021 1- TERT-BUTYL -1H-PYRAZOLE-4-C

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