Boronic acid derivatives
4-Aminobenzeneboronic acid hydrochloride, 97%
CAS: 80460-73-7 Molecular Formula: C6H9BClNO2 Molecular Weight (g/mol): 173.403 MDL Number: MFCD03001333 InChI Key: QBYGJJSFMOVYOA-UHFFFAOYSA-N Synonym: 4-aminophenylboronic acid hydrochloride,4-aminophenyl boronic acid hydrochloride,4-aminobenzeneboronic acid hydrochloride,4-aminophenylboronic acid hcl,4-boronoaniline hydrochloride,4-aminophenylboronic acid, hcl,boronic acid, 4-aminophenyl-, hydrochloride,pubchem1747,4-aminophenylboronicacidhydrochloride,ksc494e4p PubChem CID: 2734614 IUPAC Name: (4-aminophenyl)boronic acid;hydrochloride SMILES: B(C1=CC=C(C=C1)N)(O)O.Cl
2,6-Dichlorophenylboronic acid, 98%, Thermo Scientific™
CAS: 73852-17-2 Molecular Formula: C6H5BCl2O2 Molecular Weight (g/mol): 190.81 MDL Number: MFCD00064869 InChI Key: CXDPUSMFYPQXCV-UHFFFAOYSA-N Synonym: 2,6-dichlorobenzeneboronic acid,2,6-dichlorophenyl boronic acid,2,6-dichlorophenylboronicacid,2,6-dichlorophenyl boranediol,boronic acid, 2,6-dichlorophenyl,pubchem7938,acmc-1bc3m,ksc489k8l,2,6-dichloro-phenylboronic acid PubChem CID: 2734332 IUPAC Name: (2,6-dichlorophenyl)boronic acid SMILES: OB(O)C1=C(Cl)C=CC=C1Cl
5-Indolylboronic acid, 97%
CAS: 144104-59-6 Molecular Formula: C8H8BNO2 Molecular Weight (g/mol): 160.97 MDL Number: MFCD01319013 InChI Key: VHADYSUJZAPXOW-UHFFFAOYSA-N Synonym: 5-indolylboronic acid,indole-5-boronic acid,1h-indol-5-yl boronic acid,1h-indole-5-boronic acid,5-indolboronic acid,5-indolyl boronic acid,5-indole-boronic acid,1h-indol-5-ylboranediol,5-indole boric acid,5-indoleboronic acid PubChem CID: 2734361 IUPAC Name: 1H-indol-5-ylboronic acid SMILES: OB(O)C1=CC=C2NC=CC2=C1
1-Cyclohexenylboronic acid pinacol ester, 97%
CAS: 141091-37-4 Molecular Formula: C12H21BO2 Molecular Weight (g/mol): 208.11 MDL Number: MFCD05663845 InChI Key: QNZFUMVTUFOLRT-UHFFFAOYSA-N Synonym: 2-cyclohex-1-en-1-yl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,1-cyclohexen-yl-boronic acid pinacol ester,cyclohexene-1-boronic acid pinacol ester,1-cyclohexen-1-yl-boronic acid pinacol ester,2-cyclohexenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,1-cyclohexeneboronic acid,2-1-cyclohexenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,cyclohexen-1-ylboronic acid, pinacol ester,2-1-cyclohexen-1-yl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,1-cyclohexeneboronic acid pinacol ester PubChem CID: 10932675 IUPAC Name: 2-(cyclohexen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane SMILES: CC1(C)OB(OC1(C)C)C1=CCCCC1
Medchemexpress LLC Ethylboronic acid | 4433-63-0 | 73.89 | 500 G
Ethylboronic acid is an organic boron compound. It serves as a versatile building block for various chemical syntheses.
- Used as a drug intermediate
- Applicable in constructing macrocycles
- Utilized in forming capsules
- Aids in the synthesis of polymers
- Integral in creating covalent organic frameworks (COFs)
Medchemexpress LLC 5-Quinolinylboronic acid | 355386-94-6 | 172.98 | 500 MG
Quinoline-5-boronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. This compound is suitable for various studies within life sciences, including its potential role as an inhibitor.
- Biochemical reagent
- Biological material
- Organic compound
- For life science related research
- Can be used as an inhibitor
Medchemexpress LLC Cyclopropylboronic acid | 411235-57-9 | MFCD04038750 | 99.2% | C3H7BO2 | 500 G
Cyclopropylboronic acid is an intermediate that can be utilized in the synthesis of EGFR kinase inhibitor (Compound 25). This compound demonstrates antiproliferative effects on EGFR mutant (EGFR Δ19del/T790M/C797S) cells, suggesting its potential use in lung cancer research.
- Used to synthesize EGFR kinase inhibitor.
- Demonstrates antiproliferative effects on EGFR mutant cells.
- Potential for use in lung cancer research.
- Inhibits proliferation of Ba/F3 triple-mutant suspension cells.
Medchemexpress LLC 3-aminophenylboronic acid | 30418-59-8 | MFCD00007755 | 99.9% | 136.94 g/mol | C6H8BNO2 | 500 G
3-Aminophenylboronic acid is an organoboron reagent used in organic synthesis and biochemical research. It serves as a building block for cross-coupling chemistry and can be functionalized for biosensing applications, such as glycoprotein recognition when attached to nanomaterials. The compound is supplied at high purity and is suitable for analytical, preparative, and material science workflows.
- High purity suitable for analytical and synthetic applications.
- Serves as a boronic acid building block for cross-coupling reactions.
- Contains a reactive amino group for derivatization and bioconjugation.
- Applicable to sensor development for selective glycoprotein detection.
- Available in packaging sizes that support scale-up and bulk use.
Cayman Chemical CAY10573 Fatty Acids and Deriv
A PPAR agonist that displays potent binding at PPARα, γ, and δ (IC50s = 113, 50, 223 nM, respectively) and potently transactivates PPARα, γ, and δ (EC50s = 8, 70, 500 nM, respectively); demonstrates stronger binding and functional activity for PPARγ than rosiglitazone
Cayman Chemical CAY10573 Fatty Acids and Deriv
A PPAR agonist that displays potent binding at PPARα, γ, and δ (IC50s = 113, 50, 223 nM, respectively) and potently transactivates PPARα, γ, and δ (EC50s = 8, 70, 500 nM, respectively); demonstrates stronger binding and functional activity for PPARγ than rosiglitazone
Cayman Chemical CAY10573 Fatty Acids and Deriv
A PPAR agonist that displays potent binding at PPARα, γ, and δ (IC50s = 113, 50, 223 nM, respectively) and potently transactivates PPARα, γ, and δ (EC50s = 8, 70, 500 nM, respectively); demonstrates stronger binding and functional activity for PPARγ than rosiglitazone
Cayman Chemical CAY10573 Fatty Acids and Deriv
A PPAR agonist that displays potent binding at PPARα, γ, and δ (IC50s = 113, 50, 223 nM, respectively) and potently transactivates PPARα, γ, and δ (EC50s = 8, 70, 500 nM, respectively); demonstrates stronger binding and functional activity for PPARγ than rosiglitazone