(4-(n-Cyclopropylsulfamoyl)phenyl)boronic acid

Name: (4-(n-Cyclopropylsulfamoyl)phenyl)boronic acid
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CAS No. 871329-67-8
Cat. No. CS-0175163
Purity≥95%
MDL No.None

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(4-(n-Cyclopropylsulfamoyl)phenyl)boronic acid|CS-0175163

Structure of 871329-67-8

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General Information

CAS No. 871329-67-8
Cat. No. CS-0175163
Purity ≥95%
MDL No. None
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₉H₁₂BNO₄S
Molecular Weight 241.07
Synonym(s) N-Cyclopropyl 4-boronobenzenesulfonamide
SMILES O=S(C1=CC=C(B(O)O)C=C1)(NC2CC2)=O

Description

This boronic acid features a cyclopropylsulfamoyl group at the para position, enhancing solubility and metabolic stability. The boronate moiety enables efficient Suzuki-Miyaura coupling under mild conditions, facilitating rapid assembly of biaryl scaffolds in medicinal chemistry and materials synthesis.

Application

(4-(n-Cyclopropylsulfamoyl)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. The cyclopropylsulfamoyl group imparts enhanced metabolic stability and favorable solubility properties, while the boronic acid functionality offers excellent bench stability and compatibility with diverse functional groups. This compound facilitates rapid access to pharmacologically relevant aryl motifs in medicinal chemistry and materials science applications.

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 86.63
LogP -1.1929
H_Acceptors 4
H_Donors 3
Rotatable_Bonds 4

Other Classifications

Building Blocks Functional Group Boronic Acid And Its Ester

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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(4-(n-Cyclopropylsulfamoyl)phenyl)boronic acid

CAS No. 871329-67-8

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