10284-63-6 | D-Pinitol

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$11.00	$8.00
250mg	97%	in stock	$16.00	$11.00
1g	97%	in stock	$23.00	$17.00
5g	97%	in stock	$71.00	$50.00
25g	97%	in stock	$231.00	$162.00
100g	97%	in stock	$708.00	$496.00
250g	97%	in stock	$1,600.00	$1,120.00

Description

• Catalog Number: AE08038
• Chemical Name: D-Pinitol
• CAS Number: 10284-63-6
• Molecular Formula: C7H14O6
• Molecular Weight: 194.1825
• MDL Number: MFCD00216659
• SMILES: CO[C@@H]1[C@@H](O)[C@@H](O)[C@@H]([C@@H]([C@H]1O)O)O

Computed Properties

• Complexity: 158
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 4
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 5
• Rotatable Bond Count: 1
• XLogP3: -3.2

Upstream Synthesis Route

## D-Pinitol: Enhancing Chemical Synthesis Possibilities Utilized as a versatile compound in chemical synthesis applications, D-Pinitol, also known as 3-O-methyl-D-chiro-inositol, presents significant potential for a variety of reactions. This naturally occurring compound, commonly sourced from leguminous plants, boasts a unique structure that enables it to serve as a valuable building block in numerous synthetic pathways.D-Pinitol's chemical properties lend themselves to various synthesis processes, offering opportunities for the creation of complex organic molecules through strategic manipulation of its functional groups. Its hydroxyl groups, in particular, make it a valuable reagent for the formation of esters, ethers, and other derivatives essential in the production of pharmaceuticals, agrochemicals, and fine chemicals.Furthermore, the chiral nature of D-Pinitol provides a valuable platform for asymmetric synthesis, allowing chemists to access enantiomerically pure compounds crucial in drug development and other industries requiring high-purity substances. By leveraging D-Pinitol's stereochemistry, researchers can achieve efficient and selective transformations, facilitating the creation of advanced molecular architectures with precise control over stereochemical outcomes.In addition to its role as a synthetic building block, D-Pinitol can also function as a chiral ligand in transition metal catalysis, enabling catalytic transformations that are both economical and environmentally friendly. By harnessing its unique structural features, chemists can unlock innovative catalytic pathways that lead to the rapid synthesis of valuable compounds with enhanced efficiency and selectivity.Overall, D-Pinitol's diverse applications in chemical synthesis make it a valuable tool for advancing the field of organic chemistry, driving the development of new synthetic strategies and enabling the efficient production of complex molecules with desired stereochemical properties.