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O-(6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-α,β-D-glucopyranosyl) trichloroacetimidate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135415-92-8

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  • O-(6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-α,β-D-glucopyranosyl) trichloroacetimidate

    Cas No: 135415-92-8

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135415-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135415-92-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,4,1 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 135415-92:
(8*1)+(7*3)+(6*5)+(5*4)+(4*1)+(3*5)+(2*9)+(1*2)=118
118 % 10 = 8
So 135415-92-8 is a valid CAS Registry Number.

135415-92-8Relevant articles and documents

PROCESS FOR THE PRODUCTION OF FONDAPARINUX SODIUM

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Paragraph 0067-0069, (2017/01/31)

The present invention provides improved processes of preparing Fondaparinux sodium comprising converting a compound of formula ABCDE4 to Fondaparinux sodium at a reaction pH of no more than about 9.0. In some embodiments, the intermediates for the synthes

PROCESS FOR THE PRODUCTION OF FONDAPARINUX SODIUM

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Paragraph 0094-0097, (2017/02/24)

The present invention refers to a fly step compounds of formula ABC5 novel sodium [...] provides manufacturing method: In some embodiments, step for the synthesis intermediates are sodium [...] fly is provided in addition. (by machine translation)

PROCESS FOR THE PRODUCTION OF FONDAPARINUX SODIUM

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Paragraph 0060; 0061, (2015/02/19)

The present invention provides novel processes for the preparation of Fondaparinux sodium by using the compound of formula ABC5 In some embodiments, the intermediates for the synthesis of Fondaparinux sodium, are also provided.

PROCESS FOR THE PRODUCTION OF FONDAPARINUX SODIUM

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Paragraph 0046; 0047, (2015/02/19)

The present invention provides improved processes of preparing Fondaparinux sodium comprising converting a compound of formula ABCDE4 to Fondaparinux sodium at a reaction pH of no more than about 9.0. In some embodiments, the intermediates for the synthes

PROCESS FOR THE PRODUCTION OF FONDAPARINUX SODIUM

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Paragraph 0046, (2015/02/19)

The present invention provides novel processes for the preparation of Fondaparinux sodium by using the compound of formula ABC5. In some embodiments, the intermediates for the synthesis of Fondaparinux sodium, are also provided.

PROCESS FOR THE PRODUCTION OF FONDAPARINUX SODIUM

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Paragraph 0038, (2015/02/19)

The present invention provides improved processes of preparing Fondaparinux sodium comprising converting a compound of formula ABCDE4 to Fondaparinux sodium at a reaction pH of no more than about 9.0. In some embodiments, the intermediates for the synthes

Total synthesis of anticoagulant pentasaccharide fondaparinux

Li, Tiehai,Ye, Hui,Cao, Xuefeng,Wang, Jiajia,Liu, Yonghui,Zhou, Lifei,Liu, Qiang,Wang, Wenjun,Shen, Jie,Zhao, Wei,Wang, Peng

, p. 1071 - 1080 (2014/05/20)

The anticoagulant pentasaccharide fondaparinux was synthesized using an improved and optimized synthetic strategy including a convergent [3+2] coupling approach, orthogonal protecting groups and various glycosyl donors. The new methods of glycosylation were also used for controlling the stereochemical configuration and improving the yield of the glycosylation. In addition, HPLC and NMR methods to monitor the process of total synthesis of fondaparinux were employed. This work provides a comprehensive elaboration for the synthesis and analysis of fondaparinux based on related literature, as well as abundant information for the synthesis of heparin-like oligosaccharides. A matter of protection! The anticoagulant pentasaccharide fondaparinux was synthesized using an improved and optimized synthetic strategy. The process of total synthesis was monitored by HPLC and NMR. This work will contribute to continued improvement of the multistep production of fondaparinux and provide abundant information for the synthesis of heparin-like oligosaccharides.

A synthetic approach to aromatic aminoglycoside as a neamine mimic

Inoue, Ryo,Matsuda, Sho,Oda, Yoshiki,Ooyama, Hirofumi,Yoshida, Akihiro,Hamasaki, Keita,Yamanoi, Takashi

experimental part, p. 1335 - 1343 (2012/03/27)

This paper describes the synthetic approach to an aromatic a-glycoside as a mimic of neamine, which is a common core structure of some aminoglycoside antibiotics. We achieved the synthesis of the protected precursor of the neamine mimic, 4-(2,6-diamino-2,

Modular synthesis of heparin oligosaccharides

Orgueira, Hernan A.,Bartolozzi, Alessandra,Schell, Peter,Litjens, Remy E. J. N.,Palmacci, Emma R.,Seeberger, Peter H.

, p. 140 - 169 (2007/10/03)

A general, modular strategy for the first completely stereoselective synthesis of defined heparin oligosaccharides is described. Six monosaccharide building blocks (four differentially protected glucosamines, one glucuronic and one iduronic acid) were uti

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