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N-(p-chlorophenyl)-α-D-glucopyranosylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72002-97-2

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72002-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72002-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72002-97:
(7*7)+(6*2)+(5*0)+(4*0)+(3*2)+(2*9)+(1*7)=92
92 % 10 = 2
So 72002-97-2 is a valid CAS Registry Number.

72002-97-2Downstream Products

72002-97-2Relevant academic research and scientific papers

Mechanism of the transition-metal-catalyzed mutarotation reaction of N-(p-chlorophenyl)-β-D-glucopyranosylamine in methanol

Smiataczowa, Kazimiera,Kosmalski, Jaroslaw,Widernik, Teresa,Warnke, Zygmunt

, p. 969 - 975 (2003)

Rate constants for the mutarotation reaction of N-(p-chlorophenyl)-β-D-glucopyranosylamine (NGlc) in methanol have been determined in the presence of transition metal chlorides (MCl2), at 25°C. The activity of the metal ions catalyzing the α-py

Mechanism of the hydrogen chloride/methanol-catalyzed mutarotation reaction of N-(p-chlorophenyl)-β-D-glucopyranosylamine

Smiataczowa, Kazimiera,Maj, Katarzyna,Skurski, Piotr

, p. 4269 - 4274 (2001)

The rate of the hydrogen chloride/methanol-catalyzed mutarotation of N-(p-chlorophenyl)-β-D-glucopyranosylamine has been studied polarimetrically at 16, 20, 25, and 30 °C. Rate constants and activation parameters have been determined for two parallel reac

Influence of alkali metal chlorides on the rate of mutarotation of N-(p-chlorophenyl)-β-D-glucopyranosylamine in methanol

Smiataczowa,Maj

, p. 429 - 437 (2007/10/03)

The rate of benzoic acid catalyzed mutarotation reaction of N-(p-chlorophenyl)-β-D-glucopyranosylamine has been studied in the presence of LiCl, NaCl, KCl, RbCl, CsCl, NH4Cl and (CH3)4NCl in methanol and in methanolic benz

Kinetics of the hydrogen chloride/methanol-catalyzed mutarotation reaction of N-(p-chlorophenyl)-β-D-glucopyranosylamine

Smiataczowa

, p. 1513 - 1522 (2007/10/03)

The rate of hydrogen chloride-catalyzed mutarotation reaction of N-(p-chlorophenyl)-β-D-glucopyranosylamine has been studied polarimetrically in absolute methanol at 25°C. Depending on the HCI concentration, conversion of isomer β to isomer α has been fou

Kinetics and mechanism of acid catalysis in the mutarotation reaction of N-(p-chlorophenyl)-β-D-glucopyranosylamine in methanolic benzoate buffer solutions

Smiataczowa,Maj,Korewa

, p. 831 - 839 (2007/10/03)

Rate constants of the mutarotation reaction of N-(p-chlorophenyl)-β-D-glucopyranosylamine have been determined in methanolic benzoate buffer solutions of various benzoic acid/sodium benzoate molar concentration ratios, at 25°C. The measurements were repea

Dissociation Constants of Carboxylic Acids and Phenols in Methanol Determined by the Catalytic Method

Smiataczowa, K.,Wawrzynow, A.,Korewa, R.

, p. 1306 - 1314 (2007/10/02)

Catalytic constants, kc, have been determined for the weak acid-catalyzed mutarotation reaction of N-(p-chlorophenyl)-β-D-glucopyranosyloamine in methanol, at 25 deg C.The Broensted law of catalysis has been exploited for calculations of new di

Acid Catalysis in the Mutarotation of N-(p-Chlorophenyl)-β-D-glucopyranosylamine in Methanolic Medium

Smiataczowa, Kazimiera

, p. 1593 - 1598 (2007/10/02)

The relationship has been studied between the rate of mutarotation of N-(p-chlorophenyl)-β-D-glucopyranosylamine and the concentration of a variety of substituted benzoic acids in methanol at 25 deg C.Catalytic constants of these acids and of 2,6-dinitrop

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