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4-O-(6-O-triphenylmethyl-β-D-galactopyranosyl)-(1->4)-1,6-anhydro-β-D-glucopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73139-43-2

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73139-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73139-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,3 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73139-43:
(7*7)+(6*3)+(5*1)+(4*3)+(3*9)+(2*4)+(1*3)=122
122 % 10 = 2
So 73139-43-2 is a valid CAS Registry Number.

73139-43-2Downstream Products

73139-43-2Relevant academic research and scientific papers

Preparation of novel 1,6-anhydro-β-lactose derivatives for the synthesis of N-acetyllactosamine-containing oligosaccharides

Tsuda, Tetsuro,Furuike, Tetsuya,Nishimura, Shin-Ichiro

, p. 411 - 416 (2007/10/03)

Versatile intermediates for the syntheses of cell-surface oligosaccharides bearing N-acetyllactosamine units have been prepared from a readily available 1,6-anhydro-β-lactose as a key starting material. Regioselective chemical manipulations of 1,6-anhydro

Novel 1,6-Anhydro-β-lactose Derivatives for Rapid and Efficient Syntheses of Oligosaccharide Sequences Containing N-Acetyllactosamine

Nishimura, Shin-Ichiro,Murayama, Sadao,Kurita, Keisuke,Kuzuhara, Hiroyoshi

, p. 1413 - 1416 (2007/10/02)

Fully functionalized glycosyl acceptors for the efficient syntheses of cell-surface carbohydrate determinants containing N-acetyllactosamine have been systematically prepared by the regioselective manipulations of a readily available 1,6-anhydro-6'-O-trit

STUDIES ON SIALIC ACIDS. V. SYNTHESIS OF α- AND β-D-Neu5Acp-(2->6)-LACTOSE

Furuhata, Kimio,Anazawa, Katsuko,Itoh, Masayoshi,Shitori, Yoshiyasu,Ogura, Haruo

, p. 2725 - 2731 (2007/10/02)

The reaction of methyl 5-acetamide-4,7,8,9-tetra-O-acetyl-2-chloro-2,3,5-trideoxy-D-glycero-β-Dgalacto-2-nonulopyranosonate with 1,6-anhydro-2,2',3,3',4'-penta-O-benzyl-β-D-lactose in the presence of mercury cyanide and mercury bromide gave a 1:1 mixture

SYNTHESIS OF 1,6-ANHYDRO-2,3-DI-O-BENZOYL-4-O-(METHYL 2,3,4-TRI-O-BENZOYL-α-L-IDOPYRANOSYLURONATE)-β-D-GLUCOPYRANOSE FROM CELLOBIOSE

Ichikawa, Yoshitaka,Kuzuhara, Hiroyoshi

, p. 117 - 129 (2007/10/02)

The title compound (21) was synthesized from cellobiose as a synthon of a heparin-related oligosaccaride.The per-O-benzyl and per-O-benzoyl derivatives of 1,6-anhydro-4-O-(6-deoxy-β-D-xylo-hex-5-enopyranosyl)-β-D-glucopyranose were treated with a nonsolva

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