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Methylboronic acid, 97%
CAS: 13061-96-6 | CH5BO2 | 59.86 g/mol
$95.49 - $289.51
Chemical Identifiers
| CAS | 13061-96-6 |
|---|---|
| Molecular Formula | CH5BO2 |
| Molecular Weight (g/mol) | 59.86 |
| MDL Number | MFCD00002105 |
| InChI Key | KTMKRRPZPWUYKK-UHFFFAOYSA-N |
| Synonym | methaneboronic acid, methyl boronic acid, dihydroxymethylborane, boronic acid, methyl, unii-8z1me41sch, methane boronic acid, 8z1me41sch, methylboronicacid, methyboronic acid, methyl-boronic acid |
| PubChem CID | 139377 |
| IUPAC Name | methylboronic acid |
| SMILES | CB(O)O |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAL1558903
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Thermo Scientific Chemicals
L1558903 |
1 g |
Each for $95.49
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AAL1558906
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Thermo Scientific Chemicals
L1558906 |
5 g |
Each for $289.51
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Description
Reagent used for palladium-catalyzed stille and suzuki-miyaura cross-couplings, microwave-heated heterogeneous palladium (pd)-catalytized reactions, ruthenium (ru)-catalyzed silylation reactions, bis(aminotropone) titanium (ti) catalysts for ethylene polymerizations, enantioselective asymmetric bromoaminocyclization and bromoaminocyclization using amino-thiocarbamate catalysts. Reagent used in preparation of common building blocks for pharmaceuticals and agrochemicals, chrysin analogs by suzuki-miyaura coupling reactions, casein kinase i inhibitors, divergent c-h functionalizations directed by sulfonamide pharmacophores in drug discovery.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsReagent used for palladium-catalyzed stille and suzuki-miyaura cross-couplings, microwave-heated heterogeneous palladium (pd)-catalytized reactions, ruthenium (ru)-catalyzed silylation reactions, bis(aminotropone) titanium (ti) catalysts for ethylene polymerizations, enantioselective asymmetric bromoaminocyclization and bromoaminocyclization using amino-thiocarbamate catalysts. Reagent used in preparation of common building blocks for pharmaceuticals and agrochemicals, chrysin analogs by suzuki-miyaura coupling reactions, casein kinase i inhibitors, divergent c-h functionalizations directed by sulfonamide pharmacophores in drug discovery.
Solubility
Soluble in water.
Notes
Hygroscopic.Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, water, moisture.
Identifiants chimiques
| 13061-96-6 | |
| 59.86 | |
| KTMKRRPZPWUYKK-UHFFFAOYSA-N | |
| 139377 | |
| CB(O)O |
| CH5BO2 | |
| MFCD00002105 | |
| methaneboronic acid, methyl boronic acid, dihydroxymethylborane, boronic acid, methyl, unii-8z1me41sch, methane boronic acid, 8z1me41sch, methylboronicacid, methyboronic acid, methyl-boronic acid | |
| methylboronic acid |
Spécifications
| 13061-96-6 | |
| Odorless | |
| CH3B(OH)2 | |
| 1 g | |
| Hygroscopic | |
| Soluble in water. | |
| CB(O)O | |
| 59.86 | |
| 59.86 | |
| Methylboronic acid |
| 89°C to 94°C | |
| CH5BO2 | |
| MFCD00002105 | |
| 1731087 | |
| methaneboronic acid, methyl boronic acid, dihydroxymethylborane, boronic acid, methyl, unii-8z1me41sch, methane boronic acid, 8z1me41sch, methylboronicacid, methyboronic acid, methyl-boronic acid | |
| KTMKRRPZPWUYKK-UHFFFAOYSA-N | |
| methylboronic acid | |
| 139377 | |
| 97% |
Sécurité et manipulation
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
missing translation for 'tsca' : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only