(4-Bromo-2-methoxyphenyl)methanol

Name: (4-Bromo-2-methoxyphenyl)methanol
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CAS No. 17102-63-5
Cat. No. CS-W005395
Purity≥98%
MDL No.MFCD07369762

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(4-Bromo-2-methoxyphenyl)methanol|CS-W005395

Structure of 17102-63-5

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General Information

CAS No. 17102-63-5
Cat. No. CS-W005395
Purity ≥98%
MDL No. MFCD07369762
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₈H₉BrO₂
Molecular Weight 217.06
Synonym(s) 4-BROMO-2-METHOXYBENZYL ALCOHOL 97
SMILES COC1=C(CO)C=CC(Br)=C1

Description

This boronate moiety integrates a bromo-substituted methoxyphenyl group with a primary alcohol, enabling direct functionalization in cross-coupling reactions. The para-bromo and ortho-methoxy pattern enhances reactivity while maintaining bench-stable handling under standard conditions.

Application

(4-Bromo-2-methoxyphenyl)methanol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the benzylic position. Its bromo group facilitates palladium-catalyzed cross-coupling reactions, while the methoxy substituent provides moderate electron-donating character and ortho-directing effects. The benzylic alcohol functionality offers a handle for oxidation, protection, or derivatization, supporting diverse synthetic routes. Bench-stable and readily purified by flash chromatography, it functions effectively in multi-step syntheses of bioactive heterocycles and pharmaceutical intermediates.

Safety Information

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GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302
Precautionary Statements : P264-P270-P330-P501

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Computational Chemistry Data

TPSA 29.46
LogP 1.95
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 2

Other Classifications

Building Blocks Functional Group Bromide

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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(4-Bromo-2-methoxyphenyl)methanol

CAS No. 17102-63-5

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