14686-89-6 | 1,2:5,6-Di-O-isopropylidene-alpha-D-gulofuranose

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$8.00	$5.00
1g	98%	in stock	$10.00	$7.00
5g	98%	in stock	$20.00	$14.00
10g	98%	in stock	$36.00	$25.00
25g	98%	in stock	$89.00	$62.00

Description

• Catalog Number: AA65138
• Chemical Name: 1,2:5,6-Di-O-isopropylidene-alpha-D-gulofuranose
• CAS Number: 14686-89-6
• Molecular Formula: C12H20O6
• Molecular Weight: 260.2836
• MDL Number: MFCD00080776
• SMILES: O[C@@H]1[C@@H](O[C@H]2[C@@H]1OC(O2)(C)C)[C@H]1COC(O1)(C)C

Computed Properties

• Complexity: 342
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 5
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1

Upstream Synthesis Route

Diacetone-D-Glucose is a versatile compound that is commonly used in chemical synthesis due to its unique properties. This compound serves as a valuable building block in the creation of various organic molecules and has found applications in a wide range of industries.In chemical synthesis, Diacetone-D-Glucose is frequently employed as a protecting group for hydroxyl functionalities. By temporarily modifying the hydroxyl group with Diacetone-D-Glucose, chemists can selectively manipulate other functional groups without affecting the original hydroxyl functionality. This protection strategy is essential in the synthesis of complex molecules where multiple functional groups need to be controlled and manipulated with precision.Additionally, Diacetone-D-Glucose can be utilized as a chiral building block in asymmetric synthesis. Its unique structure allows for the creation of enantiopure compounds, which are crucial in the pharmaceutical and fine chemical industries. By incorporating Diacetone-D-Glucose into a synthesis pathway, chemists can access specific stereoisomers with high levels of efficiency and selectivity.Overall, the application of Diacetone-D-Glucose in chemical synthesis enables chemists to streamline complex reactions, control regioselectivity, and access enantiomerically pure compounds, making it a valuable tool in modern organic chemistry.