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Methyl 2-(acetylamino)-4,6-O-benzylidene-2-deoxyhexopyranosid-3-ulose is a complex organic compound with the molecular formula C16H19NO6. It is a derivative of a sugar molecule, specifically a deoxyhexopyranosid, which has undergone several modifications. The compound features a methyl group attached to the acetylamino functional group, and the 4 and 6 positions of the sugar ring are connected to a benzylidene group, which is a phenylmethylidyne group. The 3 position of the sugar ring is in the form of a ulose, indicating an oxidation state that is characteristic of a ketone or aldehyde. methyl 2-(acetylamino)-4,6-O-benzylidene-2-deoxyhexopyranosid-3-ulose is likely to be found in the field of organic chemistry, particularly in the synthesis of complex carbohydrates and related bioactive molecules, and may have potential applications in pharmaceuticals or materials science due to its unique structure and reactivity.

4288-74-8

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4288-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4288-74-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4288-74:
(6*4)+(5*2)+(4*8)+(3*8)+(2*7)+(1*4)=108
108 % 10 = 8
So 4288-74-8 is a valid CAS Registry Number.

4288-74-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(6-methoxy-8-oxo-2-phenyl-4a,6,7,8a-tetrahydro-4H-pyrano[3,2-d][1,3]dioxin-7-yl)acetamide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:4288-74-8 SDS

4288-74-8Relevant academic research and scientific papers

3- and 4-uloses derived from N-acetyl- D -glucosamine: A unique pair of complementary organocatalysts for asymmetric epoxidation of alkenes

Schoeberl, Christof,Jaeger, Volker

, p. 790 - 796 (2012/05/04)

The 4-ulose and the 3-ulose, both derived in two steps from the α-methyl glycoside of N-acetyl-D-glucosamine (GlcNAc), act as organocatalysts in the asymmetric epoxidation of alkenes, with unprecedented complementary enantioselectivity. The best results are found with α,β-unsaturated esters as substrates, with enantiomeric ratios up to 90:10 and 11:89, respectively. Copyright

Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: dialkylzinc-aldehyde additions.

Emmerson, Daniel P G,Villard, Renaud,Mugnaini, Claudia,Batsanov, Andrei,Howard, Judith A K,Hems, William P,Tooze, Robert P,Davis, Benjamin G

, p. 3826 - 3838 (2007/10/03)

The ready construction of 24 stereochemically and functionally diverse carbohydrate ligand structures from a core D-glucosamine scaffold has allowed the evaluation of broad ranging structure activity relationships in ligand accelerated zincate additions t

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