101691-65-0 | (Tetrahydropyran-4-yl)methyl tosylate

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$30.00	$21.00
10g	98%	in stock	$50.00	$35.00

Description

• Catalog Number: AA06590
• Chemical Name: (Tetrahydropyran-4-yl)methyl tosylate
• CAS Number: 101691-65-0
• Molecular Formula: C13H18O4S
• Molecular Weight: 270.3446
• MDL Number: MFCD09475806
• SMILES: Cc1ccc(cc1)S(=O)(=O)OCC1CCOCC1

Computed Properties

• Complexity: 333
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• XLogP3: 2

Upstream Synthesis Route

The compound (Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulfonate finds significant utility in chemical synthesis as a versatile reagent and protecting group. Its unique structure containing a tetrahydro-2H-pyran moiety provides a valuable platform for introducing diversity in organic molecules. In the realm of chemical synthesis, this compound serves as an effective reagent for the selective protection of hydroxyl groups in various organic molecules. By acting as a protecting group, it allows chemists to manipulate and control the reactivity of hydroxyl functionalities in complex molecular structures, thereby enabling the selective modification of target molecules. This capability is particularly valuable in the synthesis of natural products, pharmaceuticals, and other complex organic compounds where precise chemical transformations are required. Additionally, the (Tetrahydro-2H-pyran-4-yl)methyl 4-methylbenzenesulfonate can facilitate the construction of intricate molecular frameworks through strategic deprotection steps, paving the way for efficient and controlled synthetic routes. Its application in chemical synthesis highlights its importance as a valuable tool for chemists seeking to navigate the intricacies of organic reactions and achieve precise control over molecular functionalization.