Boronic acid derivatives

eMolecules​ 5720-06-9 | 2-Methoxyphenylboronic acid | ChemScene | MFCD00236047 | 151.960 | C7H9BO3 | 98.000 | COc1ccccc1B(O)O | 5g | 874112883

2-Methoxyphenylboronic acid | ChemScene | 5720-06-9 | MFCD00236047 | 151.960 | C7H9BO3 | 98.000 | COc1ccccc1B(O)O | 5g | 874112883

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eMolecules​ 5720-07-0 | 4-Methoxyphenylboronic acid | ChemScene | MFCD00039139 | 151.960 | C7H9BO3 | 98.000 | COc1ccc(cc1)B(O)O | 1g | 894452990

4-Methoxyphenylboronic acid | ChemScene | 5720-07-0 | MFCD00039139 | 151.960 | C7H9BO3 | 98.000 | COc1ccc(cc1)B(O)O | 1g | 894452990

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eMolecules​ 5720-07-0 | 4-Methoxyphenylboronic acid | Ambeed | MFCD00039139 | 151.960 | C7H9BO3 | 98.000 | COc1ccc(cc1)B(O)O | 100g | 490558423

4-Methoxyphenylboronic acid | Ambeed | 5720-07-0 | MFCD00039139 | 151.960 | C7H9BO3 | 98.000 | COc1ccc(cc1)B(O)O | 100g | 490558423

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Medchemexpress LLC Butylboronic acid | 4426-47-5 | 101.94 | 10 MM * 1 ML

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Butylboronic acid is a competitive soybean urease inhibitor with an IC50 of 2.9 mM and a Ki of 1.5 mM.

• Competitive soybean urease inhibitor (IC50 of 2.9 mM and a Ki of 1.5 mM).
• Promotes cell proliferation, alkaline phosphatase activity, and expression of GJA1, ALP, and NaBC1 in human dental pulp cells in vitro.

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Aobchem Thiophene-2-boronic acid pinacol ester | ≥97% | CAS 193978-23-3 | C10H15BO2S | 25g

Thiophene-2-boronic acid pinacol ester | ≥97% | CAS 193978-23-3 | C10H15BO2S | 25g

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Aobchem Neopentyl methanesulfonate | ≥95% | CAS 16427-42-2 | C6H14O3S | 10g

Neopentyl methanesulfonate | ≥95% | CAS 16427-42-2 | C6H14O3S | 10g

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Aobchem Thiophene-2-boronic acid pinacol ester | ≥97% | CAS 193978-23-3 | C10H15BO2S | 1kg

Thiophene-2-boronic acid pinacol ester | ≥97% | CAS 193978-23-3 | C10H15BO2S | 1kg

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TARGETMOL CHEMICALS INC Phenothiazine Analogues 1MG

Also available in 5 mg, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. 3-Amino-1-(2-chloro-10H-phenothiazin-10-yl)-1-propanone is involved in the synthesis of phenothiazine series compounds. Purity 98%

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eMolecules​ 411235-57-9 | Cyclopropylboronic acid | ChemScene | MFCD04038750 | 85.900 | C3H7BO2 | 95.000 | OB(O)C1CC1 | 500g | 582637519

Cyclopropylboronic acid | ChemScene | 411235-57-9 | MFCD04038750 | 85.900 | C3H7BO2 | 95.000 | OB(O)C1CC1 | 500g | 582637519

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eMolecules​ 72824-04-5 | Allylboronic acid pinacol ester,98%(stabilized with Phenothiazine) | ChemScene | MFCD00013347 | 168.040 | C9H17BO2 | 98.000 | CC1(C)OB(CC=C)OC1(C)C | 25g | 536841435

Allylboronic acid pinacol ester,98%(stabilized with Phenothiazine) | ChemScene | 72824-04-5 | MFCD00013347 | 168.040 | C9H17BO2 | 98.000 | CC1(C)OB(CC=C)OC1(C)C | 25g | 536841435

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eMolecules​ 126726-62-3 | Isopropenylboronic acid pinacol ester | Ambeed | MFCD08276843 | 168.040 | C9H17BO2 | 98.000 | CC(=C)B1OC(C)(C)C(C)(C)O1 | 5g | 526391936

Isopropenylboronic acid pinacol ester | Ambeed | 126726-62-3 | MFCD08276843 | 168.040 | C9H17BO2 | 98.000 | CC(=C)B1OC(C)(C)C(C)(C)O1 | 5g | 526391936

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eMolecules​ 3-CYANOPHENYLBORONIC ACID 25G

5000159961 3-CYANOPHENYLBORONIC ACID 25G

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eMolecules​ 472805-74-6 | 4-Methyl-2-(2-methoxyphenyl)thiazole-5-carboxylic acid | Oakwood Chemical | MFCD06857926 | 249.280 | C12H11NO3S | 98.000 | COc1ccccc1-c1nc(C)c(s1)C(O)=O | 5g | 537688035

4-Methyl-2-(2-methoxyphenyl)thiazole-5-carboxylic acid | Oakwood Chemical | 472805-74-6 | MFCD06857926 | 249.280 | C12H11NO3S | 98.000 | COc1ccccc1-c1nc(C)c(s1)C(O)=O | 5g | 537688035

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Medchemexpress LLC 3-Aminophenylboronic acid monohydrate | 206658-89-1 | 154.96 | 10 G

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3-Aminophenylboronic acid monohydrate is a biochemical reagent useful as a biological material or organic compound for life science related research. It is intended for research use only and not for sale to patients.

• Reagent in the preparation of Suzuki-Miyaura cross-coupling
• Used for Gram-positive anti-virulence drugs and inhibitors of Streptococcus agalactiae Stk1
• Regioisomer of Zaleplon, a sedative
• Amphiphilic random glycopolymer that forms nanoparticles
• Chemomechanical polymer that expands and contracts in blood plasma with high glucose selectivity
• Reagent in the preparation of nonbenzodiazepine hypnotic agents

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eMolecules​ 862081-37-6 | ChemScene | 5-(4455-Tetramethyl-132-dioxaborolan-2-yl)isobenzofuran-1(3H)-one | 250mg | 559783437 | CS-W020496 | MFCD18251723 | 260.1 | C14H17BO4

ChemScene | 5-(4455-Tetramethyl-132-dioxaborolan-2-yl)isobenzofuran-1(3H)-one | 250mg | 559783437 | CS-W020496 | 862081-37-6 | MFCD18251723 | 260.100 | C14H17BO4

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