3-(Aminomethyl)benzeneboronic acid hydrochloride, 96%
3-(Aminomethyl)benzeneboronic acid hydrochloride, 96%
3-(Aminomethyl)benzeneboronic acid hydrochloride, 96%
3-(Aminomethyl)benzeneboronic acid hydrochloride, 96%
Thermo Scientific Chemicals

3-(Aminomethyl)benzeneboronic acid hydrochloride, 96%

CAS: 352525-94-1 | C7H11BClNO2 | 187.43 g/mol
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Quantity:
250 mg
1 g
Catalog number H53284.03
also known as H53284-03
Price (USD)
144.65
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161.00
Save 16.35 (10%)
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Quantity:
1 g
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Price (USD)
144.65
Online Exclusive
161.00
Save 16.35 (10%)
Each
Add to cart
Specifications
CAS352525-94-1
Chemical Name or Material3-(Aminomethyl)benzeneboronic acid hydrochloride
Formula Weight187.43
Health Hazard 1H315-H319-H335
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
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3-(Aminomethyl)benzeneboronic acid hydrochloride is used as intermediates. Hydroxybenzene boronic acids are involved in suzuki miyaura reactions. It is a arylboronic acid. 3-Fluoro-4-hydroxybenzeneboronic acid, can be an effective catalyst for amidation and esterification of carboxylic acids.

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
3-(Aminomethyl)benzeneboronic acid hydrochloride is used as intermediates. Hydroxybenzene boronic acids are involved in suzuki miyaura reactions. It is a arylboronic acid. 3-Fluoro-4-hydroxybenzeneboronic acid, can be an effective catalyst for amidation and esterification of carboxylic acids.

Solubility
Slightly soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents. Refrigerate.
RUO – Research Use Only

General References:

  1. Tomohiro Yasukawa et. al.Copper-catalyzed, aerobic oxidative cross-coupling of alkynes with arylboronic acids: remarkable selectivity in 2,6-lutidine media.. Organic & Biomolecular Chemistry. 2011, 9(18), 6208-6210.