1,2-O-Isopropylidene-α-D-glucofuranose

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1,2-O-Isopropylidene-α-D-glucofuranose

Original price was: $795.00.Current price is: $395.00.

Catalog Number: B2027244 (1 g)
1,2-O-Isopropylidene-α-D-glucofuranose is a protected monosaccharide derivative widely utilized as a key building block and intermediate in organic synthesis, carbohydrate chemistry, and biotechnology. Derived from D-glucose, it features an isopropylidene group that selectively protects the hydroxyl groups at the C-1 and C-2 positions, providing increased stability and reactivity control during chemical transformations. Supplied as a high-purity crystalline powder, this reagent is essential for the selective synthesis of glycosides and complex biomolecules. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

1,2-O-Isopropylidene-α-D-glucofuranose
Catalog number: B2027244
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 220.22
Supplied as: Powder
Storage: NA
Keywords: Monoacetone Glucose, Acetone Glucose, Acetone-D-Glucose, 1,2-O-Isopropylidene-alpha-D-glucofuranose, Mono-Acetone-D-Glucose

References:
1. Kovacevic SZ, Jevric LR, Podunavac-Kuzmanovic SO, Loncar ES. Prediction of in-silico ADME properties of 1,2-O-isopropylidene aldohexose derivatives. Acta Chimica Slovenica. 2014;61(1):145-155.
2. Schmidt OT. 1,2-O-Isopropylidene-alpha-D-glucofuranose. Methods in Carbohydrate Chemistry. 1963;2:318-325.
3. Gramera RE, Park A, Whistler RL. Pyrolysis of 1,2-O-isopropylidene-alpha-D-glucofuranose. Journal of Organic Chemistry. 1963;28(11):3230-3232.
4. Brimacombe JS, Gent PA, Stacey M. Nucleophilic replacement reactions of 1,2-O-isopropylidene-alpha-D-glucofuranose derivatives. Carbohydrate Research. 1968;6(4):499-503.
5. Glen AT, Morrison A, Tener GM. Derivatization and selective reactions of 1,2-O-isopropylidene-alpha-D-glucofuranose. Journal of the Chemical Society C: Organic. 1966;(12):1120-1127.
6. Srivastava RM, Bakhru M. Synthesis and structural studies of modified 1,2-O-isopropylidene-alpha-D-glucofuranose compounds. Carbohydrate Research. 1981;93(1):141-147.
7. Fleet GW, Witty DR. Synthesis of polyhydroxylated pyrrolidines from 1,2-O-isopropylidene-alpha-D-glucofuranose. Tetrahedron: Asymmetry. 1990;1(2):119-124.
8. Rao VS, Perlin AS. Regioselectivity in reactions of 1,2-O-isopropylidene-alpha-D-glucofuranose. Canadian Journal of Chemistry. 1983;61(4):652-657.
9. Whistler RL, Lake WC. Selective functionalization of 1,2-O-isopropylidene-alpha-D-glucofuranose. Methods in Carbohydrate Chemistry. 1972;6:286-291.
10. Kawsar SM, Islam M, Jelir S. Synthesis, characterization, and biological evaluation of 1,2-O-isopropylidene-alpha-D-glucofuranose derivatives. Journal of the Bangladesh Chemical Society. 2018;30(1):31-38.
1,2-O-Isopropylidene-α-D-glucofuranose

Products Related to 1,2-O-Isopropylidene-α-D-glucofuranose can be found at Carbohydrates

Additional Information

Weight 0.15 oz
Dimensions 2 × 0.5 × 0.5 in
5/5 - (1 vote)

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