107869-45-4 | (3aR,6S)-8,8-dimethyl-4,5,6,7-tetrahydro-3h-3a,6-methanobenzo[c]isothiazole 2,2-dioxide

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$10.00	$7.00
5g	98%	in stock	$33.00	$23.00
25g	98%	in stock	$112.00	$79.00

Description

• Catalog Number: AB54456
• Chemical Name: (3aR,6S)-8,8-dimethyl-4,5,6,7-tetrahydro-3h-3a,6-methanobenzo[c]isothiazole 2,2-dioxide
• CAS Number: 107869-45-4
• Molecular Formula: C10H15NO2S
• Molecular Weight: 213.2966
• MDL Number: MFCD00064576
• SMILES: O=S1(=O)N=C2[C@@]3(C1)CC[C@@H](C2)C3(C)C

Computed Properties

• Complexity: 430
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• XLogP3: 1.1

Upstream Synthesis Route

(3aR,6S)-8,8-Dimethyl-4,5,6,7-tetrahydro-3H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide is a valuable compound in chemical synthesis due to its unique structural features. This compound can serve as a versatile building block in the creation of various organic molecules. Its bicyclic structure containing both sulfur and oxygen atoms makes it a useful intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.In organic synthesis, (3aR,6S)-8,8-Dimethyl-4,5,6,7-tetrahydro-3H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide can participate in a range of reactions to introduce functional groups or modify existing functionalities. Its rigid framework and stereochemical configuration provide opportunities for selective transformations, allowing for the creation of complex molecules with high structural diversity.Furthermore, the presence of the sulfur dioxide moiety in this compound can enable it to act as a sulfinylating agent, facilitating the introduction of sulfinyl groups into target molecules. This reactivity expands the synthetic utility of (3aR,6S)-8,8-Dimethyl-4,5,6,7-tetrahydro-3H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide in the design and construction of novel compounds with specific biological or physical properties.Overall, the strategic incorporation of (3aR,6S)-8,8-Dimethyl-4,5,6,7-tetrahydro-3H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide into synthetic pathways offers chemists a powerful tool for the efficient and selective generation of diverse molecular architectures tailored to particular applications in the fields of pharmaceuticals, materials science, and beyond.