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methyl 2-O-benzoyl-4,6-O-benzylidene-α-D-xylo-hexopyranosid-3-ulose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109010-31-3

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109010-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109010-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,0,1 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 109010-31:
(8*1)+(7*0)+(6*9)+(5*0)+(4*1)+(3*0)+(2*3)+(1*1)=73
73 % 10 = 3
So 109010-31-3 is a valid CAS Registry Number.

109010-31-3Relevant academic research and scientific papers

Enolates of carbohydrates, 5. Syntheses of axially methyl-branched pyranosiduloses

Klemer, Almuth,Klaffke, Werner

, p. 759 - 764 (2007/10/02)

The α-C-methylated carbohydrates 3 and 5 are available from the benzoyl- and benzylidene protected 2- and 3-uloses 1a, 2, and 4 by reaction with potassium tert-butoxide/methyl iodide in N,N-dimethylformamide.Under pthe same conditions the 2-O-benzyl-3-ulose 1b yields the enol ether 6a, and the enolone 8 is obtained from the 2-O-benzoyl-3-ulose 7.

Arylazo-glycenosides. Part 8. Synthesis and Reactions of Some 2- and 3-Arylazo-derivatives of Methyl 4,6-O-Benzylidene-2,3-dideoxy-D-threo-hex-2-enopyranosides

Dang, Neeta,Munasinghe, Ranjith N.,Overend, W. George

, p. 257 - 264 (2007/10/02)

Preparations are described of the α- and β-anomers of methyl 4,6-O-benzylidene-2,3-dideoxy-2-phenylazo-D-threo-hex-2-enopyranoside and of methyl 4,6-O-benzyliden-2,3-dideoxy-3-phenylazo-α-D-threo-hex-2-enopyranoside using D-galactose as the initial materi

Branched-chain Sugars. XXIV. Synthesis of Methyl 6-Deoxy-3-C-methyl-β-D-gulopyranoside (Methyl β-Virenoside)

Hong, Namgi,Sato, Ken-ichi,Yoshimura, Juji

, p. 2379 - 2382 (2007/10/02)

Methyl 6-deoxy-3-C-methyl-β-D-gulopyranoside (methyl β-virenoside) was prepared from D-galactose.An attempted synthesis of the virenoside by the inversion at C-4 of methyl 6-deoxy-3C-methyl-α-D-allopyranoside was unsuccessful.

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