5-Bromo-1H-indol-6-amine

Name: 5-Bromo-1H-indol-6-amine
Brand: ChemScene
Availability: InStock
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CAS No. 873055-33-5
Cat. No. CS-0043008
Purity≥97%
MDL No.MFCD09880057

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Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
Inaccessible (Haz class 6.1 or 9), Domestic	$68.00+
Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
Accessible (Haz class 3, 4, 5 or 8), International	$238.00+

An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

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*For research and further manufacturing use only, not for direct human use.

Structure of 873055-33-5

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Description

5-Bromo-1H-indol-6-amine features a bromine substituent at the 5-position and a primary amine at the 6-position of the indole core. This configuration enables direct incorporation into Suzuki-Miyaura couplings and other cross-coupling reactions, facilitating rapid access to functionalized indole derivatives for medicinal chemistry and materials science applications.

Application

5-Bromo-1H-indol-6-amine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the 6-position via palladium-catalyzed cross-coupling reactions. Its bromo group exhibits high reactivity in Suzuki, Stille, and Negishi transformations, while the pendant amine facilitates conjugation or derivatization under mild conditions. The molecule demonstrates excellent bench stability and is readily purified by standard chromatographic methods, making it well-suited for scalable synthesis of indole-based pharmaceuticals and kinase inhibitors.

General Information

CAS No. 873055-33-5
Cat. No. CS-0043008
Purity ≥97%
MDL No. MFCD09880057
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₈H₇BrN₂
Molecular Weight 211.06
Synonym(s) 6-Amino-5-bromoindole
SMILES NC1=CC2=C(C=CN2)C=C1Br

Computational Chemistry Data

TPSA 41.81
LogP 2.5126
H_Acceptors 1
H_Donors 2
Rotatable_Bonds 0

Safety Information

Download SDS

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

Quality Control

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Other Classifications

Building Blocks Functional Group Bromide

Building Blocks Skeleton Aromatic heterocycle compounds Indole compounds

Key Words

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5-Bromo-1H-indol-6-amine

CAS No. 873055-33-5

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