Boronic acid derivatives
eMolecules 214360-73-3 | 4-Aminophenylboronic acid, pinacol ester | Synthonix - Stock | MFCD02093721 | 219.090 | C12H18BNO2 | 98.000 | CC1(C)OB(OC1(C)C)c1ccc(N)cc1 | 1g | 525905267
4-Aminophenylboronic acid, pinacol ester | Synthonix - Stock | 214360-73-3 | MFCD02093721 | 219.090 | C12H18BNO2 | 98.000 | CC1(C)OB(OC1(C)C)c1ccc(N)cc1 | 1g | 525905267
Cambridge Isotope Laboratories Modified JIS Dioxin Furan Calibration Solution (CS7H) 0 2 mL
Modified JIS Dioxin Furan Calibration Solution (CS7H) 0 2 mL
eMolecules 14047-29-1 | 4-Carboxyphenylboronic acid | Key Organics/BIONET | MFCD00151801 | 165.940 | C7H7BO4 | 90.000 | OB(O)c1ccc(cc1)C(O)=O | 10mg | 564101494
4-Carboxyphenylboronic acid | Key Organics/BIONET | 14047-29-1 | MFCD00151801 | 165.940 | C7H7BO4 | 90.000 | OB(O)c1ccc(cc1)C(O)=O | 10mg | 564101494
eMolecules 14047-29-1 | 4-Carboxyphenylboronic acid | Key Organics/BIONET | MFCD00151801 | 165.940 | C7H7BO4 | 90.000 | OB(O)c1ccc(cc1)C(O)=O | 5mg | 564101493
4-Carboxyphenylboronic acid | Key Organics/BIONET | 14047-29-1 | MFCD00151801 | 165.940 | C7H7BO4 | 90.000 | OB(O)c1ccc(cc1)C(O)=O | 5mg | 564101493
Medchemexpress LLC Oul35 (NSC39047) | 6336-34-1 | 99.8% | 256.26 g/mol | C14H12N2O3 | 50MG
OUL35 (NSC39047) is a selective small-molecule inhibitor of ARTD10/PARP10 with an in vitro IC50 of 329 nM. It is supplied as a high-purity research compound for biochemical and cell-based assays probing ADP-ribosylation and PARP-related cellular processes.
- Selective ARTD10/PARP10 inhibitor with reported IC50 of 329 nM.
- High purity suitable for research applications (99.8%).
- Molecular weight 256.26 g/mol; chemical formula C14H12N2O3.
- Soluble in DMSO; store solid at 4°C and protect from light.
- Available in small solid quantities and as DMSO solutions for assay setup.
eMolecules 72824-04-5 | Allylboronic acid, pinacol ester | Apollo Scientific US | MFCD00013347 | 168.040 | C9H17BO2 | 97.000 | CC1(C)OB(CC=C)OC1(C)C | 25g | 705605488
Allylboronic acid, pinacol ester | Apollo Scientific US | 72824-04-5 | MFCD00013347 | 168.040 | C9H17BO2 | 97.000 | CC1(C)OB(CC=C)OC1(C)C | 25g | 705605488
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
Aobchem 2 4-Dichloro-5-fluorophenylboronic acid | ≥97% | CAS 1417914-09-0 | C6H4BCl2FO2 | 1g
2 4-Dichloro-5-fluorophenylboronic acid | ≥97% | CAS 1417914-09-0 | C6H4BCl2FO2 | 1g
Aobchem 3-Bromo-2-ethoxyphenylboronic acid | ≥95% | CAS 352525-81-6 | C8H10BBrO3 | 250mg
3-Bromo-2-ethoxyphenylboronic acid | ≥95% | CAS 352525-81-6 | C8H10BBrO3 | 250mg
Matrix Scientific 3-AMINOPHENYLBORONIC ACID3--25
3-aminophenylboronic Acid Mf C6h8bno2 Mw 136.95 Cas 30418-59-8 Mdl MFCD00007755
eMolecules 72824-04-5 | Allylboronic acid pinacol ester | Ambeed | MFCD00013347 | 168.040 | C9H17BO2 | 97.000 | CC1(C)OB(CC=C)OC1(C)C | 1g | 552538916
Allylboronic acid pinacol ester | Ambeed | 72824-04-5 | MFCD00013347 | 168.040 | C9H17BO2 | 97.000 | CC1(C)OB(CC=C)OC1(C)C | 1g | 552538916
![Frontier Specialty Chemicals 5g, Bis[(pinacolato)boryl]methane, 97%, [78782-17-9], M13441 267.965 C13H26B2O4](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00026836-M13441.PNG-250.jpg)
Frontier Specialty Chemicals 5g, Bis[(pinacolato)boryl]methane, 97%, [78782-17-9], M13441 267.965 C13H26B2O4
Compound: Bis[(pinacolato)boryl]methane
CAS#: 78782-17-9
MDL#: MFCD27977747
Background: A geminal bis(boronate) reagent used in organic synthesis to introduce two independently functionalizable boron centers on a single carbon. It is a versatile building block for iterative cross-coupling and other organoboron chemistry.
Storage: Store at room temperature, under dry conditions.
Medchemexpress LLC N-Boc-diethanolamine | 25g
N-Boc-diethanolamine is an Alkyl/ether-based PROTAC linker can be used in the synthesis of PROTACs N-Boc-diethanolamine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]