N-Iodosaccharin

Name: N-Iodosaccharin
Brand: ChemScene
Availability: InStock
Rating: 5 (1 reviews)

CAS No. 86340-94-5
Cat. No. CS-0205380
Purity≥97%
MDL No.MFCD09037939

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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.

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Description

N-Iodosaccharin delivers a potent electrophilic iodine source for direct C–H functionalization and halogenation reactions. This bench-stable, moisture-tolerant reagent features a polarized N–I bond that facilitates selective iodination under mild conditions. The electron-deficient saccharin scaffold enhances reactivity while minimizing side processes.

Application

N-Iodosaccharin serves as a stable, bench-ready source of electrophilic iodine for direct C–H functionalization and heterocycle iodination. It enables regioselective mono-iodination of electron-rich aromatic systems under mild conditions, with high functional group tolerance and straightforward purification. The reagent functions effectively in both stoichiometric and catalytic applications, facilitating access to iodinated intermediates for cross-coupling and medicinal chemistry campaigns.

General Information

CAS No. 86340-94-5
Cat. No. CS-0205380
Purity ≥97%
MDL No. MFCD09037939
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₇H₄INO₃S
Molecular Weight 309.08
Synonym(s) 2-Iodo-1,2-benzisothiazol-3(2H)-one 1,1-Dioxide
SMILES O=C1C=2C=CC=CC2S(=O)(=O)N1I

Computational Chemistry Data

TPSA 54.45
LogP 1.1811
H_Acceptors 3
H_Donors 0
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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362

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N-Iodosaccharin

CAS No. 86340-94-5

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