6-Amino-1-indanone

Name: 6-Amino-1-indanone
Brand: ChemScene
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CAS No. 69975-65-1
Cat. No. CS-W020513
Purity≥95%
MDL No.MFCD00100747

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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.

There is a HazMat shipping fee for each item that qualifies as a dangerous good. Please contact our quotation team via email to confirm the details.

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

Structure of 69975-65-1

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Description

6-Amino-1-indanone features a fused bicyclic core with an amino group at the 6-position, delivering enhanced electron density and reactivity. This bench-stable scaffold integrates readily into pharmaceutical intermediates and functional materials, offering improved solubility in polar solvents and compatibility with standard synthetic protocols.

Application

6-Amino-1-indanone serves as a versatile building block in medicinal chemistry, enabling the synthesis of indanone-based scaffolds through standard functional group transformations. Its amino group facilitates nucleophilic substitution, amidation, and coupling reactions, while the ketone moiety supports enolate formation and reductive amination. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it valuable for iterative synthesis workflows.

General Information

CAS No. 69975-65-1
Cat. No. CS-W020513
Purity ≥95%
MDL No. MFCD00100747
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₉H₉NO
Molecular Weight None
Synonym(s) 6-Aminoindanone
SMILES O=C1CCC2=C1C=C(N)C=C2

Computational Chemistry Data

TPSA 43.09
LogP 1.3977
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 0

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS06
Signal Word : Danger	UN#: 2811
Class : 6.1	Packing Group : Ⅲ
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P264-P270-P330-P405-P501

Quality Control

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Other Classifications

Building Blocks Functional Group Ketone

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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6-Amino-1-indanone

CAS No. 69975-65-1

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