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cyclohexyl 3,4,6-tri-O-benzyl-2-deoxy-2-iodo-α-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84207-52-3

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84207-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84207-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84207-52:
(7*8)+(6*4)+(5*2)+(4*0)+(3*7)+(2*5)+(1*2)=123
123 % 10 = 3
So 84207-52-3 is a valid CAS Registry Number.

84207-52-3Downstream Products

84207-52-3Relevant academic research and scientific papers

Phenyl 2-Deoxy-2-iodo-1-thio-glycosides: New Glycosyl Donors for the Stereo-selective Synthesis of 2-Deoxy-oligosaccharides

Arnés, Xavier,Díaz, Yolanda,Castillón, Sergio

, p. 2143 - 2146 (2003)

Phenyl 2-deoxy-2-iodo-1-thioglycosides, prepared from simple pentoses by olefination and iodine-induced cyclization, have proved to be efficient glycosyl donors for the stereoselective synthesis of 2-deoxy-2-iodo- oligosaccharides, which are precursors of

Bronsted Acids of Anionic Chiral Cobalt(III) Complexes as Catalysts for the Iodoglycosylation or Iodocarboxylation of Glycals

Wang, Rui,Wu, Wen-Qiang,Li, Na,Shen, Jia,Liu, Kun,Yu, Jie

supporting information, p. 1077 - 1084 (2019/05/24)

Bronsted acids of anionic chiral Co(III) complexes were found to act as efficient phase-transfer catalysts for the diastereoselective iodoglycosylation or iodocarboxylation of glycals with a variety of alcohols or carboxylic acids, respectively, with N -iodosuccinimide as the iodo cation source. The corresponding 2-deoxy-2-iodoglycosides, including monosaccharides and disaccharides, and 2-deoxy-2-iodoglycosyl carboxylates, which are of high synthetic and biological importance, were obtained in high yields (up to 88%) with good diastereoselectivities (up to 9:1 dr).

Glycosylations of Glycals using N-Iodosuccinimide (NIS) and Phosphorus Compounds for Syntheses of 2-Iodo- and 2-Deoxyglycosides

Kimura, Tomoya,Takahashi, Daisuke,Toshima, Kazunobu

, p. 9552 - 9562 (2015/10/12)

The glycosylations of glycals and alcohols using N-iodosuccinimide (NIS) and a catalytic amount of PPh3 effectively proceeded under mild conditions to provide the corresponding 2-deoxy-2-iodoglycosides in high yields. The reactivity of the iodo

HIGHLY STEREOSELECTIVE SYNTHESIS OF α-D-GLUCOPYRANOSIDES BY THE N-IODOSUCCINIMIDE-PROMOTED INTERNAL CYCLIZATION

Suzuki, Keisuke,Mukaiyama, Teruaki

, p. 1525 - 1528 (2007/10/02)

Highly stereoselective cyclizations of hydroxy enol ethers are effected by N-iodosuccinimide to result in the exclusive formation of 2'-deoxy-2'iodo-α-D-glucopyranosides.An analog of glycolipid is also successfully synthesized according to the present met

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