α-D-Glucopyranoside, 2-propenyl 2,3-bis-O-(phenylmethyl)- (9CI), with the CAS number 87326-32-7, is a glycoside derivative of glucose. This compound features a glucopyranoside structure, which is a six-membered cyclic form of glucose, and is modified with two phenylmethyl (benzyl) groups at the 2 and 3 positions, enhancing its lipophilicity and potentially its biological activity. The presence of a propenyl group indicates that it has an unsaturated carbon chain, which may contribute to its reactivity and interactions in various chemical environments. This compound is likely to exhibit properties typical of glycosides, such as solubility in polar solvents and potential applications in organic synthesis or as a biochemical probe. Its structural modifications suggest potential uses in medicinal chemistry or as a building block in the synthesis of more complex molecules. As with many glycosides, it may also exhibit specific biological activities, although detailed studies would be necessary to elucidate its exact properties and applications.

a-D-Glucopyranoside, 2-propenyl2,3-bis-O-(phenylmethyl)- (9CI)

87326-32-7: α-D-Glucopyranoside, 2-propenyl 2,3-bis-O-(phenylmethyl)- (9CI), with the CAS number 87326-32-7, is a glycoside derivative of glucose. This compound features a glucopyranoside structure, which is a six-membered cyclic form of glucose, and is modified with two phenylmethyl (benzyl) groups at the 2 and 3 positions, enhancing its lipophilicity and potentially its biological activity. The presence of a propenyl group indicates that it has an unsaturated carbon chain, which may contribute to its reactivity and interactions in various chemical environments. This compound is likely to exhibit properties typical of glycosides, such as solubility in polar solvents and potential applications in organic synthesis or as a biochemical probe. Its structural modifications suggest potential uses in medicinal chemistry or as a building block in the synthesis of more complex molecules. As with many glycosides, it may also exhibit specific biological activities, although detailed studies would be necessary to elucidate its exact properties and applications.

Allyl 2,3-di-O-benzyl-a-D-glucopyranoside

<p>Allyl 2,3-di-O-benzyl-a-D-glucopyranoside is a plant growth regulator that stimulates callus formation. It belongs to the group of auxins and has been shown to promote callus growth in Arabidopsis thaliana cultivars, such as glaberrima and kinetin. This compound has also been shown to stimulate the formation of calli from coconut explants.</p>

CAS 87326-32-7

a-D-Glucopyranoside, 2-propenyl2,3-bis-O-(phenylmethyl)- (9CI)

Allyl 2,3-di-O-benzyl-a-D-glucopyranoside

Ref: 7W-GC4346

Allyl 2,3-di-O-benzyl-a-D-glucopyranoside

Ref: 3D-MA02906