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The chemical "(2S,3R,4E)-[4'-O-(β-D-galactopyranosyl)-β-D-glucopyranosyl]-(1'->1)-2-(hexadecanoylamido)-4-octadecene-1,3-diol" is a complex glycolipid molecule. It consists of a glycerol backbone with two hydroxyl groups at the 1 and 3 positions, and a double bond in the 4 position, indicating an E-configuration. The molecule is further characterized by the presence of a hexadecanoylamide group (a fatty acid amide) at the 2 position, which is a common feature in lipids. Additionally, it has a β-D-glucopyranosyl group linked to a β-D-galactopyranosyl group, which are sugar moieties, with the galactose being attached to the glucose in a 4'-O-glycosidic linkage. This structure is typical of certain glycosphingolipids, which are important components of cell membranes and play roles in cell recognition and signaling. The specific stereochemistry at the glycerol backbone (2S,3R) and the double bond (4E) are crucial for its biological activity and interactions.

7084-64-2

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7084-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7084-64-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,8 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7084-64:
(6*7)+(5*0)+(4*8)+(3*4)+(2*6)+(1*4)=102
102 % 10 = 2
So 7084-64-2 is a valid CAS Registry Number.

7084-64-2Downstream Products

7084-64-2Relevant academic research and scientific papers

Borinic acid-catalyzed stereo- and site-selective synthesis of β-glycosylceramides

D'Angelo, Kyan A.,Taylor, Mark S.

, p. 5978 - 5980 (2017)

A method for activation of unprotected ceramides towards stereo- and site-selective glycosylation is described. Two-point binding of a diarylborinic acid catalyst to the ceramide accelerates its reactions with 'armed' glycosyl methanesulfonate donors, resulting in the formation of a β-glycosidic linkage at the primary OH group.

Efficient syntheses of a series of glycosphingolipids with 1,2-trans-glycosidic linkages

Liu, Yunpeng,Ding, Ning,Xiao, Hualing,Li, Yingxia

, p. 471 - 489 (2007/10/03)

A series of glycosphingolipids with 1,2-trans-glycosidic linkages were synthesized in the presence of neighboring group participation using trichloroacetimidates as glycosyl donors and an azido-sphingosine as the glycosyl acceptor. During the preparation

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