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Acetic acid (1S,2R,3S)-2,3-bis-benzyloxy-4-hydroxy-6-oxo-cyclohexyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110372-54-8

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110372-54-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110372-54-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,3,7 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 110372-54:
(8*1)+(7*1)+(6*0)+(5*3)+(4*7)+(3*2)+(2*5)+(1*4)=78
78 % 10 = 8
So 110372-54-8 is a valid CAS Registry Number.

110372-54-8Relevant academic research and scientific papers

Synthesis of Optically Active Substituted Cyclohexenones from Carbohydrates by Catalytic Ferrier Rearrangement

Chida, Noritaka,Ohtsuka, Masami,Ogura, Katsuyuki,Ogawa, Seiichiro

, p. 2118 - 2121 (2007/10/02)

Conversion of hex-5-enopyranosides into substituted cyclohexenones (Ferrier rearrangement) was found to proceed efficiently with a catalytic amount of various mercury(II) salts at room temperature in a neutral solvent system.Among the mercury(II) salts tested, mercury(II) trifluoroacetate showed the highest activity.Four optically active cyclohexenones were prepared from hex-5-enopyranosides utilizing this method.

Total Synthesis of Antibiotic Hygromycin A

Chida, Noritaka,Ohtsuka, Masami,Nakazawa, Keiichi,Ogawa, Seiichiro

, p. 2976 - 2983 (2007/10/02)

The first total synthesis of the antibiotic (-)-hygromycin A (1) has been achieved by a coupling reaction of the sugar moiety (2) and the cyclitol moiety (3).Both components were synthesized in homochiral forms starting from D-glucose.This synthesis fully

α-Glucosidase Inhibitors, 5.- Investigations towards a Synthesis of C1-Branched Cyclitols from D-Glucose

Koehn, Arnim,Schmidt, Richard R.

, p. 1045 - 1054 (2007/10/02)

The glucose derivatives 1 and 2 were transformed by Ferrier rearrangement as one of the reaction steps into the cyclitol derivatives 3a,b and 4a,b, respectively.The attachment of a functional C1-side chain at the carbonyl group was tested with

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