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3-(Hydroxymethyl)benzeneboronic acid, 98%, Thermo Scientific Chemicals

Catalog Number p-7046604
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Quantity:
1 g
5 g
This item is not returnable. View return policy
To receive the discount customers must purchase three of the same product at list price in a single order to receive 33.33% discount. There is no limit to the multiples of 3 that customers can buy. Use promo code ”21615” to get your promotional price
87199-15-3
C7H9BO3
151.96
MFCD01317846
HGTDLKXUWVKLQX-UHFFFAOYSA-N
3-hydroxymethyl phenylboronic acid, 3-hydroxymethylphenylboronic acid, 3-hydroxymethyl phenyl boronic acid, 3-hydroxymethyl benzeneboronic acid, 3-boronobenzyl alcohol, 3-hydroxymethylphenyl boronic acid, 3-hydroxymethyl phenylboronicacid, 3-hydroxymethyl phenyl boranediol, 3-boronophenyl methanol
2734662
[3-(hydroxymethyl)phenyl]boronic acid
OCC1=CC=CC(=C1)B(O)O
This item is not returnable. View return policy
To receive the discount customers must purchase three of the same product at list price in a single order to receive 33.33% discount. There is no limit to the multiples of 3 that customers can buy. Use promo code ”21615” to get your promotional price
87199-15-3
C7H9BO3
151.96
MFCD01317846
HGTDLKXUWVKLQX-UHFFFAOYSA-N
3-hydroxymethyl phenylboronic acid, 3-hydroxymethylphenylboronic acid, 3-hydroxymethyl phenyl boronic acid, 3-hydroxymethyl benzeneboronic acid, 3-boronobenzyl alcohol, 3-hydroxymethylphenyl boronic acid, 3-hydroxymethyl phenylboronicacid, 3-hydroxymethyl phenyl boranediol, 3-boronophenyl methanol
2734662
[3-(hydroxymethyl)phenyl]boronic acid
OCC1=CC=CC(=C1)B(O)O

Reactant used for copper-mediated trifluoromethylation, copper-catalyzed transformations from arylboronic acids in water, Mitsunobu, Suzuki, and amidation reactions with hydroxyphenylamino bromopyrazinecarboxylate. Reactant involved in the synthesis of biologically active molecules including Mycobacterium tuberculosis H37Rv chorismate mutase inhibitors via Suzuki coupling reactions, HIV protease inhibitors with antiviral activity against drug-resistant viruses, Pyrrole derivatives for use as PDE4B inhibitors.

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.

Applications
Reactant used for copper-mediated trifluoromethylation, copper-catalyzed transformations from arylboronic acids in water, Mitsunobu, Suzuki, and amidation reactions with hydroxyphenylamino bromopyrazinecarboxylate. Reactant involved in the synthesis of biologically active molecules including Mycobacterium tuberculosis H37Rv chorismate mutase inhibitors via Suzuki coupling reactions, HIV protease inhibitors with antiviral activity against drug-resistant viruses, Pyrrole derivatives for use as PDE4B inhibitors.

Solubility
Soluble in water.

Notes
Store in cool. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
TRUSTED_SUSTAINABILITY
Melting Point 93°C to 98°C
Quantity 1 g
Beilstein 8832019
Solubility Information Soluble in water.
Formula Weight 151.96
Percent Purity 98%
Chemical Name or Material 3-(Hydroxymethyl)benzeneboronic acid

RUO – Research Use Only

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