(2-Amino-3-bromophenyl)methanol

Name: (2-Amino-3-bromophenyl)methanol
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CAS No. 397323-70-5
Cat. No. CS-0042660
Purity≥97%
MDL No.None

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(2-Amino-3-bromophenyl)methanol|CS-0042660

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General Information

CAS No. 397323-70-5
Cat. No. CS-0042660
Purity ≥97%
MDL No. None
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₇H₈BrNO
Molecular Weight 202.05
Synonym(s) Ambroxol Impurity 51
SMILES OCC1=CC=CC(Br)=C1N

Description

This bench-stable arylmethanol features a brominated aromatic ring and a primary alcohol group, enabling direct incorporation into Suzuki-Miyaura couplings and other cross-coupling transformations. The ortho-amino functionality supports coordination in catalytic systems and facilitates downstream derivatization through electrophilic substitution or diazotization reactions.

Application

(2-Amino-3-bromophenyl)methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. Its ortho-amino and bromomethyl functionalities facilitate sequential functionalization via Pd-catalyzed coupling and electrophilic substitution. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for medicinal chemistry campaigns requiring modular scaffold elaboration.

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-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

TPSA 46.25
LogP 1.5236
H_Acceptors 2
H_Donors 2
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Alcohol

Building Blocks Functional Group Bromide

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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(2-Amino-3-bromophenyl)methanol

CAS No. 397323-70-5

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