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Methyl 3,6-di-O-benzoyl-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51996-11-3

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51996-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51996-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,9 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51996-11:
(7*5)+(6*1)+(5*9)+(4*9)+(3*6)+(2*1)+(1*1)=143
143 % 10 = 3
So 51996-11-3 is a valid CAS Registry Number.

51996-11-3Downstream Products

51996-11-3Relevant academic research and scientific papers

A green and convenient method for regioselective mono and multiple benzoylation of diols and polyols

Zhang, Xiaoling,Ren, Bo,Ge, Jiantao,Pei, Zhichao,Dong, Hai

, p. 1005 - 1010 (2016/02/03)

An efficient method for regioselective benzoylation of diols and polyols was developed. The benzoylation is catalyzed by only 0.2 equiv of benzoate anion in acetonitrile with the addition of a stoichiometric amount of benzoic anhydride under very mild condition, leading to high yields. Compared with all other methods, this method shows particular advantage in regioselective multiple benzoylation of polyols, and in avoiding the use of any metal-based catalysts and any amine bases, which is more environment-friendly.

Reagent-dependent regioselective control in multiple carbohydrate esterifications

Dong, Hai,Pei, Zhichao,Bystroem, Styrbjoern,Ramstroem, Olof

, p. 1499 - 1502 (2007/10/03)

(Chemical Equation Presented) Regioselective control in organotin-mediated multiple acylation of carbohydrates is presented. The acylation reagent could be efficiently used to direct the product formation. Reagent-dependent thermodynamic and kinetic contr

Regioselective acylation of carbohydrates with 1-acyloxy-1H-benzotriazoles

Pelyvas,Lindhorst,Streicher,Thiem

, p. 1015 - 1018 (2007/10/02)

Acylation of representative carbohydrate derivatives was accomplished with in situ generated 1-acyloxy-1H-benzotriazoles. The observed high regioselectivity, mild reaction conditions and convenient work-up make the presented one-pot procedure generally applicable and more advantageous than acylations with previously introduced reagents, including N-acylimidazoles.

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