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3,5-Dimethoxybenzeneboronic acid, 98%, Thermo Scientific Chemicals
61.90 € - 234.00 €
Chemical Identifiers
| CAS | 192182-54-0 |
|---|---|
| Molecular Formula | C8H11BO4 |
| Molecular Weight (g/mol) | 181.982 |
| MDL Number | MFCD03095127 |
| InChI Key | XUIURRYWQBBCCK-UHFFFAOYSA-N |
| Synonym | 3,5-dimethoxybenzeneboronic acid, 3,5-dimethoxyphenyl boronic acid, 3,5-dimethoxyphenylboronicacid, boronic acid, 3,5-dimethoxyphenyl, pubchem1827, acmc-1c82c, ksc174i6h, 3,5-dimethoxy phenyl boronic acid, 3,5-dimethoxyphenylboronic acid, boronic acid, b-3,5-dimethoxyphenyl |
| PubChem CID | 4374257 |
| IUPAC Name | (3,5-dimethoxyphenyl)boronic acid |
| SMILES | B(C1=CC(=CC(=C1)OC)OC)(O)O |
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|---|---|---|---|---|---|---|---|---|---|
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|
15409737
|
Thermo Scientific Alfa Aesar
H52965.03 |
1 g |
61.90 €
1g |
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|
15419737
|
Thermo Scientific Alfa Aesar
H52965.06 |
5 g |
234.00 €
5g |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
Description
3,5-Dimethoxybenzeneboronic acid is used as reactant for palladium-catalyzed coupling reactions, preparation of benzopyranone derivatives as positive GABAA receptor modulators, preparation of aryl alkenes via three-component coupling catalyzed by palladium and Suzuki-Miyaura coupling. It is also used as reactant for rhodium catalyzed cyanation with N-cyano-N-phenyl-p-methylbenzenesulfonamide and preparation of bisphosphonate inhibitors of human farnesyl pyrophosphate synthase.
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.
Applications3,5-Dimethoxybenzeneboronic acid is used as reactant for palladium-catalyzed coupling reactions, preparation of benzopyranone derivatives as positive GABAA receptor modulators, preparation of aryl alkenes via three-component coupling catalyzed by palladium and Suzuki-Miyaura coupling. It is also used as reactant for rhodium catalyzed cyanation with N-cyano-N-phenyl-p-methylbenzenesulfonamide and preparation of bisphosphonate inhibitors of human farnesyl pyrophosphate synthase.
Solubility
Soluble in methanol.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
Chemical Identifiers
| 192182-54-0 | |
| 181.982 | |
| XUIURRYWQBBCCK-UHFFFAOYSA-N | |
| 4374257 | |
| B(C1=CC(=CC(=C1)OC)OC)(O)O |
| C8H11BO4 | |
| MFCD03095127 | |
| 3,5-dimethoxybenzeneboronic acid, 3,5-dimethoxyphenyl boronic acid, 3,5-dimethoxyphenylboronicacid, boronic acid, 3,5-dimethoxyphenyl, pubchem1827, acmc-1c82c, ksc174i6h, 3,5-dimethoxy phenyl boronic acid, 3,5-dimethoxyphenylboronic acid, boronic acid, b-3,5-dimethoxyphenyl | |
| (3,5-dimethoxyphenyl)boronic acid |
Specifications
| 192182-54-0 | |
| C8H11BO4 | |
| 3,5-dimethoxybenzeneboronic acid, 3,5-dimethoxyphenyl boronic acid, 3,5-dimethoxyphenylboronicacid, boronic acid, 3,5-dimethoxyphenyl, pubchem1827, acmc-1c82c, ksc174i6h, 3,5-dimethoxy phenyl boronic acid, 3,5-dimethoxyphenylboronic acid, boronic acid, b-3,5-dimethoxyphenyl | |
| XUIURRYWQBBCCK-UHFFFAOYSA-N | |
| (3,5-dimethoxyphenyl)boronic acid | |
| 4374257 | |
| 98% |
| 205°C to 207°C | |
| MFCD03095127 | |
| Soluble in methanol. | |
| B(C1=CC(=CC(=C1)OC)OC)(O)O | |
| 181.982 | |
| 181.98 | |
| 3,5-Dimethoxybenzeneboronic acid |
Safety and Handling
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
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