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3-O-benzoyl-D-erythro-sphingosine is a synthetic sphingosine derivative, which is a type of sphingolipid, a class of lipids that play a crucial role in cell signaling and membrane structure. This specific compound is characterized by the presence of a benzoyl group attached to the 3-hydroxyl position of the sphingosine backbone. The D-erythro configuration refers to the stereochemistry of the molecule, indicating the spatial arrangement of its atoms. 3-O-benzoyl-D-erythro-sphingosine is often used in biochemical research to study the effects of sphingolipids on cellular processes, as it can mimic or modulate the activity of endogenous sphingosine and its metabolites. It has been implicated in the study of various biological pathways, including those involved in cell growth, differentiation, and apoptosis.

4201-60-9

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4201-60-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4201-60-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,0 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4201-60:
(6*4)+(5*2)+(4*0)+(3*1)+(2*6)+(1*0)=49
49 % 10 = 9
So 4201-60-9 is a valid CAS Registry Number.

4201-60-9Relevant academic research and scientific papers

Practical syntheses of [13C]- and [14C]-labelled glucosphingolipids

Duffin, Gordon R.,Ellames, George J.,Hartmann, Sascha,Herbert, John M.,Smith, David I.

, p. 2237 - 2242 (2007/10/03)

Synthetic routes to [glucose-U-14C]-1-O-(β-D-glucopyranosyl)-N-stearoyl-D-erythro-sp hingosine 1b and to [glucose-13C6]-1-O-(β-D-glucopyranosyl)sphingosine ([glucose-13C6]glucopsychosine, 2b) are described. Whereas the protected ceramide precursor for lb was prepared using conventional methodology, two new strategies were developed in the course of the synthesis of 2b. Of these, one relies on keeping a protecting group in place at all times to avoid the handling difficulties associated with sphingosine 4, while the other generates a protected derivative (24) of sphingosine indirectly by means of a Mitsunobu inversion.

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