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2-isopropyl-5-methylcyclohexyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16124-23-5

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16124-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16124-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,2 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16124-23:
(7*1)+(6*6)+(5*1)+(4*2)+(3*4)+(2*2)+(1*3)=75
75 % 10 = 5
So 16124-23-5 is a valid CAS Registry Number.

16124-23-5Downstream Products

16124-23-5Relevant academic research and scientific papers

Polyvinyl trisulfonate ethylamine based solid acid catalyst for the efficient glycosylation of sugars under solvent free conditions

Chaugule, Avinash A.,Jadhav, Amol R.,Kim, Hern

, p. 104715 - 104724 (2015)

Heterogeneous Bronsted solid acid catalysts have the potential to decrease the environmental impact related to chemical production. Herein, we have synthesized polyvinyl bound trisulfonate ethylamine chloride (PV-THEAC) and polyvinyl bound disulfonate ethylamine (PV-DSEA) as Bronsted solid acid catalysts which exhibited effective catalytic activity for acid catalyzed glycosylation reactions with sugar derivatives. In particular, 0.3 equiv. of the PV-THEAC catalyst was found to be the most efficient and a reusable catalyst for glycosylation reactions. A high density of the trisulfonic group (-OSO3H) contributed to the excellent catalytic activity during glycosylation. Moreover, glycosylation reactions with d-mannose, d-xylose and d-glucose have been studied with alcohol. Remarkable acceleration of the glycosylation reaction using a glycosyltrichloroacetimidate donor was obtained with the selective production of β-glycoside.

Preparation of New Terpenyl β-D-Glucopyranosides by a Modified Koenigs-Knorr Procedure.

Ackermann, Irmtraud E.,Banthorpe, Derek V.,Fordham, William D.,Kinder, John P.,Poots, Ian

, p. 79 - 82 (2007/10/02)

Ten new hemi- and monoterpenyl β-D-glucopyranosides have been prepared by a modification of the Koenigs-Knorr procedure which utilises silver fluoroacetate as a soluble catalyst coupled with the introduction of a basic ion-exchange resin to effect the deacetylation step.Most of these compounds could not be obtained in acceptable yields using the classical procedure.

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