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(1S)-1,5-anhydro-2-deoxy-1-(2,6-dimethoxyphenyl)-3,4,6-tris-O-acetyl-D-erythro-hex-2-enitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86388-87-6

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86388-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86388-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,8 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86388-87:
(7*8)+(6*6)+(5*3)+(4*8)+(3*8)+(2*8)+(1*7)=186
186 % 10 = 6
So 86388-87-6 is a valid CAS Registry Number.

86388-87-6Downstream Products

86388-87-6Relevant academic research and scientific papers

Regio- and stereoselective synthesis of 2-deoxy-C-aryl glycosides via palladium catalyzed decarboxylative reactions

Xiang, Shaohua,Cai, Shuting,Zeng, Jing,Liu, Xue-Wei

supporting information; experimental part, p. 4608 - 4611 (2011/10/13)

An efficient and versatile approach for the synthesis of 2-deoxy-C-aryl glycosides is reported. This strategy is based on a palladium-catalyzed decarboxylative Heck coupling reaction of benzoic acids and glycals. A wide variety of glycals and benzoic acid

Arylation de glycals catalysee par les sels de palladium: nouvelle synthese de C-glycosides

Czernecki, Stanislas,Dechavanne, Veronique

, p. 533 - 540 (2007/10/02)

The arylation of peracetylated glycals catalyzed by palladium salts provides a new synthesis of C-glycosides.The title reaction is applied to several aromatic compounds, including fluoro and nitro derivatives.The regioselectivity of the reaction with respect to the aromatic nucleus is explained by the formation of an arylpalladium directly from the aromatic compound and the salt.A two-step mechanism, involving syn-addition of the arylpalladium to the glycal double bond, followed by a syn-elimination is proposed and discussed.

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